L-Carnitine and CoQ10 for Male Fertility: Positive Placebo-Controlled Study Results

Nelson Vergel

Founder, ExcelMale.com
L-Carnitine and CoQ10 for Male Fertility:
The Complete Evidence-Based Guide to Improving Sperm Quality

Curated By Nelson Vergel | ExcelMale.com | Updated January 2026

Introduction​

Could a simple combination of two naturally occurring compounds hold the key to improving male fertility? For the millions of men struggling with idiopathic infertility—where conventional medical evaluation fails to identify a specific cause—the answer may lie in addressing a fundamental issue: oxidative stress. A groundbreaking 2025 randomized controlled trial has provided compelling new evidence that the combination of L-carnitine and Coenzyme Q10 (CoQ10) produces superior improvements in sperm parameters compared to either supplement alone.
Male infertility accounts for approximately 50% of all infertility cases, with idiopathic male infertility—cases without identifiable causes—representing about 30% of male factor infertility. Oxidative stress induced by reactive oxygen species (ROS) has emerged as a major underlying mechanism, damaging sperm DNA, cell membranes, and mitochondrial function. This comprehensive guide examines the latest clinical evidence on L-carnitine and CoQ10 supplementation, providing practical recommendations for men seeking to optimize their fertility potential.
You will learn how these antioxidants work at the cellular level, what the most recent clinical trials reveal about their effectiveness, optimal dosing protocols, and practical implementation strategies based on the latest peer-reviewed research.

Understanding Oxidative Stress and Male Infertility​

Reactive oxygen species (ROS) are oxygen-derived free radicals produced during normal cellular metabolism, particularly through the mitochondrial respiratory chain. In physiological concentrations, ROS are essential for normal sperm function, including capacitation, hyperactivation, and the acrosome reaction necessary for fertilization. However, when ROS production exceeds the body's antioxidant defenses, the resulting oxidative stress damages sperm in multiple ways.

How Oxidative Stress Damages Sperm​

Lipid peroxidation: Sperm plasma membranes are rich in polyunsaturated fatty acids, making them particularly vulnerable to oxidative damage. Lipid peroxidation compromises membrane integrity, affecting sperm motility and their ability to fuse with the oocyte.
DNA fragmentation: Excess ROS directly attack sperm DNA, causing single- and double-strand breaks. Sperm DNA fragmentation (SDF) is now recognized as a critical marker of male fertility potential. Studies show that SDF above 25% is associated with reduced pregnancy rates through natural conception and IUI, while values above 50% correlate with poor IVF outcomes.
Mitochondrial dysfunction: The sperm midpiece contains mitochondria that generate the ATP required for motility. Oxidative damage to mitochondrial DNA and membranes impairs energy production, directly reducing sperm motility.
Apoptotic pathways: Severe oxidative stress triggers premature apoptosis in developing sperm cells, reducing overall sperm count and increasing the proportion of abnormal forms.

L-Carnitine: The Cellular Energy Shuttle​

L-carnitine is a quaternary ammonium compound synthesized from the amino acids lysine and methionine. While approximately 25% of the body's L-carnitine is synthesized endogenously, the remaining 75% must be obtained from dietary sources, primarily red meat, poultry, fish, and dairy products. Remarkably, L-carnitine concentrations in the epididymal fluid can be up to 2,000 times higher than blood levels, reflecting its critical importance for sperm maturation and function.

Mechanisms of Action​

Energy production via β-oxidation: L-carnitine functions as an essential cofactor for transporting long-chain fatty acids across the inner mitochondrial membrane, where they undergo β-oxidation to produce ATP. This "shuttle" function is critical for sperm cells, which rely heavily on fatty acid oxidation for energy, particularly during their transit through the epididymis and their journey to the oocyte.
Antioxidant activity: Beyond its role in energy metabolism, L-carnitine acts as a direct free radical scavenger and enhances the expression and activity of key antioxidant enzymes including superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx). It reduces malondialdehyde (MDA) levels, a marker of lipid peroxidation.
Anti-apoptotic effects: L-carnitine helps protect developing sperm cells from oxidative stress-induced apoptosis by maintaining mitochondrial membrane integrity and preventing cytochrome C release.
Acetyl-L-carnitine (LAC), the acetylated form, provides readily available acetyl groups for metabolic processes and has shown particular benefits for sperm motility. Many clinical protocols use combinations of L-carnitine and acetyl-L-carnitine for optimal results.

Coenzyme Q10: The Mitochondrial Powerhouse​

Coenzyme Q10 (CoQ10), also known as ubiquinone, is a lipid-soluble compound found in the mitochondria of virtually all cells. The "Q" refers to the quinone chemical group, while "10" indicates the number of isoprenyl units in its tail. In sperm cells, CoQ10 is concentrated in the mitochondria of the midpiece, where it plays essential roles in both energy production and antioxidant defense.

Forms: Ubiquinone vs. Ubiquinol​

CoQ10 exists in two interconvertible forms: ubiquinone (the oxidized form) and ubiquinol (the reduced, active form). Ubiquinol has superior bioavailability and is the form that directly functions as an antioxidant. Sperm cells can convert ubiquinone to ubiquinol through enzymatic processes in the cytoplasm and mitochondrial membranes. For supplementation, ubiquinol may offer advantages, particularly in older men or those with reduced conversion capacity.

Mechanisms of Action​

Electron transport chain function: CoQ10 serves as an electron carrier in mitochondrial complexes I, II, and IV of the respiratory chain, essential for ATP synthesis. Optimal CoQ10 levels ensure efficient energy production for sperm motility.
Antioxidant protection: Ubiquinol is a potent lipid-soluble antioxidant that protects sperm membranes from lipid peroxidation and inhibits superoxide production. It regenerates other antioxidants, including vitamin E.
DNA protection: CoQ10 supplementation has been shown to reduce sperm DNA fragmentation by decreasing oxidative DNA damage and nitric oxide levels in seminal plasma.
Leydig cell support: By reducing oxidative stress in testicular tissue, CoQ10 may support Leydig cell function and testosterone synthesis. Clinical studies have demonstrated increases in serum testosterone following CoQ10 supplementation.

The 2025 Landmark Study: Combination Therapy Superiority​

A pivotal 2025 placebo-controlled, double-blind randomized clinical trial published in the Arab Journal of Urology by Higazy et al. has provided the most robust evidence to date comparing L-carnitine monotherapy, CoQ10 monotherapy, and combination therapy in men with idiopathic oligoasthenoteratozoospermia (OAT).

Study Design​

Two hundred men with idiopathic primary infertility and OAT were randomized into four equal groups and treated for three months. Group 1 received CoQ10 200 mg daily, Group 2 received L-carnitine 1 gram daily, Group 3 received both CoQ10 200 mg and L-carnitine 1 gram daily, and Group 4 received placebo. Of these, 174 patients completed the study (43 in CoQ10, 42 in L-carnitine, 44 in combination, and 45 in placebo groups).

Key Findings​

Table 1: Sperm Parameter Changes After 3 Months of Treatment

Parameter

CoQ10
L-Carnitine
Combination
Placebo
Sperm Concentration
13.4→26.9 M/mL​
13.3→20.2 M/mL​
12.9→32.9 M/mL
13.2→13.8 M/mL​
Progressive Motility
23.3%→34.9%​
22.6%→29.4%​
23.3%→38.5%
24.6%→25.8%​
Total Motility
38.2%→45.6%​
37.2%→40.3%​
38.3%→50.2%
38.8%→39.2%​
Normal Morphology
18.8%→25.5%​
19.3%→22.5%​
18.8%→29.9%
19.2%→20.1%​
DNA Fragmentation Index
31.2%→19.2%​
29.6%→23.6%​
30.4%→13.9%
30.8%→29.6%​
Note: Green-highlighted cells indicate the best results. All active treatment groups showed statistically significant improvements (p<0.001) compared to placebo.

The Power of Combination Therapy​

The study's most significant finding was the superiority of combination therapy over monotherapy with either agent alone. The combination group achieved a remarkable 155% increase in sperm concentration (from 12.9 to 32.9 million/mL), compared to 100% for CoQ10 monotherapy and 52% for L-carnitine monotherapy. Even more striking, the DNA fragmentation index dropped from 30.4% to 13.9% with combination therapy—a 54% reduction that brought values well below the clinically significant threshold of 25%.
These results support the biological rationale for combination therapy: L-carnitine and CoQ10 act through complementary mechanisms. While L-carnitine primarily supports fatty acid transport and energy production while scavenging ROS, CoQ10 optimizes mitochondrial electron transport and provides lipid-soluble antioxidant protection. Together, they address multiple pathways of oxidative damage simultaneously.

Effects on Reproductive Hormones​

The Higazy study also revealed significant hormonal changes with antioxidant therapy. Testosterone levels increased significantly in all active treatment groups: from 3.98 to 5.73 ng/mL with CoQ10 (+44%), from 4.57 to 4.97 ng/mL with L-carnitine (+9%), and from 3.87 to 6.51 ng/mL with combination therapy (+68%). The placebo group showed no significant change.
Accompanying these testosterone increases, FSH and LH levels decreased in the treatment groups, suggesting improved testicular function rather than compensatory hormone elevation. This pattern indicates that antioxidants may reduce oxidative stress in Leydig cells, enhancing their capacity for testosterone synthesis. Importantly, prolactin levels remained unchanged across all groups, indicating no adverse effects on this hormonal axis.
Table 2: Hormonal Changes After 3 Months of Treatment

Hormone

CoQ10
L-Carnitine
Combination
Placebo
Testosterone (ng/mL)
3.98→5.73​
4.57→4.97​
3.87→6.51
3.86→3.93​
FSH (mIU/mL)
8.50→6.41​
8.30→7.14​
8.56→5.17
8.65→8.22​
LH (mIU/mL)
8.07→5.24​
8.35→6.95​
8.12→4.45
8.09→7.86​

Supporting Evidence from Meta-Analyses​

The findings from the 2025 Higazy trial are consistent with and strengthened by several meta-analyses examining antioxidant therapy for male infertility.

2025 Network Meta-Analysis (Niu et al.)​

A comprehensive 2025 network meta-analysis published in Reproductive Sciences analyzed 16 studies comparing carnitine and CoQ10 interventions. The analysis found that CoQ10 produced the highest increase in sperm concentration (SMD 2.98), while L-carnitine was the most effective treatment for enhancing sperm motility. Both L-carnitine and L-carnitine combined with acetyl-L-carnitine significantly improved sperm quality parameters compared to placebo.

2025 Systematic Review on CoQ10 (World Journal of Men's Health)​

A 2025 systematic review and meta-analysis specifically examining CoQ10 for idiopathic male infertility found that CoQ10 supplementation significantly improved semen quality, seminal CoQ10 levels, and clinical pregnancy rates. Subgroup analysis revealed that treatment duration greater than 3 months was associated with significant improvements in sperm morphology. The review also confirmed CoQ10's excellent safety profile, with studies reporting no serious adverse effects.

2022 Network Meta-Analysis (Li et al.)​

A 2022 network meta-analysis published in Frontiers in Endocrinology comparing various antioxidants concluded that L-carnitine had the highest probability of being the most effective treatment for increasing sperm motility and morphology, while omega-3 fatty acids and CoQ10 showed the greatest effects on sperm concentration. This complementary profile supports the rationale for combination therapy.

Dosing Recommendations and Practical Protocols​

Based on the available clinical evidence, the following dosing protocols have demonstrated efficacy for improving sperm parameters in men with idiopathic infertility:
Table 3: Evidence-Based Dosing Protocols

Supplement

Dose
Duration
Evidence Level
L-Carnitine
1,000-3,000 mg/day​
≥3 months (ideally 6)​
Strong (RCTs)​
Acetyl-L-Carnitine
500-2,000 mg/day​
≥3 months​
Strong (RCTs)​
CoQ10 (Ubiquinone)
200-300 mg/day​
≥3 months (ideally 6)​
Strong (RCTs)​
CoQ10 (Ubiquinol)
100-200 mg/day​
≥3 months​
Moderate​

Practical Implementation Tips​

Timing: Take supplements with meals containing fat to enhance absorption, particularly for CoQ10 which is fat-soluble.
Duration: Since spermatogenesis takes approximately 72 days, a minimum of 3 months of supplementation is necessary to see effects on mature sperm. Many studies showing the best results used 6-month protocols.
Testing: Obtain baseline semen analysis before starting supplementation. Repeat analysis at 3 months and 6 months to assess response.
DNA fragmentation testing: Consider sperm DNA fragmentation testing (TUNEL, SCD, or SCSA) if available, as this may be more sensitive to antioxidant therapy than conventional semen parameters.
Lifestyle factors: Antioxidant supplementation should complement, not replace, lifestyle modifications including smoking cessation, moderate alcohol consumption, maintaining healthy weight, and avoiding testicular heat exposure.

Safety and Side Effects​

Both L-carnitine and CoQ10 have excellent safety profiles based on decades of clinical use and research. The 2025 Higazy trial reported no significant adverse effects in any treatment group. L-carnitine is FDA-approved for treatment of carnitine deficiency in hemodialysis patients, reflecting its established safety even at therapeutic doses.
Potential side effects are generally mild and uncommon: L-carnitine may occasionally cause gastrointestinal symptoms (nausea, diarrhea) or a "fishy" body odor at high doses. CoQ10 is well-tolerated, with rare reports of mild insomnia if taken late in the day or mild GI upset.
Drug interactions: CoQ10 may interact with warfarin (potentially reducing anticoagulant effect) and some chemotherapy agents. L-carnitine has few significant interactions but may enhance the effects of thyroid hormone medications. Men taking prescription medications should consult their healthcare provider before starting supplementation.
Caution regarding excessive antioxidant use: Some research suggests that very high doses of antioxidants may paradoxically increase oxidative stress or interfere with normal cellular signaling. Stick to evidence-based dosing ranges rather than assuming "more is better."

Who Should Consider L-Carnitine and CoQ10?​

Based on current evidence, L-carnitine and CoQ10 supplementation may be particularly beneficial for:
• Men with idiopathic oligoasthenoteratozoospermia (OAT) or abnormalities in any semen parameter
• Men with elevated sperm DNA fragmentation (≥20-25%)
• Couples planning IVF/ICSI, particularly those with previous poor fertilization rates
• Men with lifestyle factors known to increase oxidative stress (smoking history, obesity, environmental exposures)
• Men over 40 who may have age-related decline in endogenous antioxidant capacity
• Men on TRT seeking to optimize remaining testicular function or preserve fertility with adjunctive hCG therapy

Limitations and Considerations​

While the evidence supporting L-carnitine and CoQ10 for male fertility is increasingly robust, several limitations should be acknowledged. The MOXI (Males, Antioxidants, and Infertility) trial, a large multicenter RCT, failed to show significant improvements in semen parameters or DNA integrity with a combination antioxidant supplement. However, critics note that the MOXI study population may not have had elevated oxidative stress at baseline, potentially explaining the negative results.
Most studies have focused on semen parameters rather than pregnancy rates or live birth rates—the outcomes that ultimately matter most to couples. The 2025 Higazy study did not evaluate pregnancy outcomes. Additionally, optimal dosing, duration, and which specific formulations work best remain areas requiring further research.
Finally, improvements in semen parameters after discontinuing therapy tend to gradually reverse, suggesting that continued supplementation may be necessary to maintain benefits. The Higazy study showed that treatment effects persisted but declined over a 12-week treatment-free period in some parameters.

Conclusion​

The 2025 Higazy trial represents a significant advancement in our understanding of antioxidant therapy for male infertility, providing the first rigorous comparison of L-carnitine, CoQ10, and combination therapy in a placebo-controlled setting. The clear superiority of combination therapy—with sperm concentration more than doubling and DNA fragmentation dropping by over 50%—provides compelling evidence for using both supplements together rather than relying on either alone.
For men with idiopathic infertility or suboptimal semen parameters, a protocol combining L-carnitine (1,000 mg/day) and CoQ10 (200 mg/day) for at least 3 months represents an evidence-based, well-tolerated approach that addresses multiple pathways of oxidative sperm damage. While antioxidant supplementation should not replace evaluation for treatable causes of infertility, it offers a low-risk intervention that can meaningfully improve sperm quality and potentially enhance fertility outcomes.

Key References​

1. Higazy A, Mohammed W, Esmat M, Samir M. Evaluation of monotherapy of Coenzyme Q10, L-carnitine or combined therapy on semen parameters in idiopathic male infertility. Arab Journal of Urology. 2026;24(1):68-74. doi:10.1080/20905998.2025.2509424
2. Niu C, Lu X, Xie Y, et al. Effects of Carnitine and Coenzyme Q10 on Sperm Quality and Pregnancy Rates in Men with Unexplained Infertility: A Systematic Review and Network Meta-Analysis. Reproductive Sciences. 2025;32(9):2864-2876. PMID: 40813743
3. Li KP, Yang XS, Wu T. The Effect of Antioxidants on Sperm Quality Parameters and Pregnancy Rates for Idiopathic Male Infertility: A Network Meta-Analysis. Frontiers in Endocrinology. 2022;13:810242. doi:10.3389/fendo.2022.810242
4. Alahmar AT, Sengupta P, Dutta S, Calogero AE. Coenzyme Q10, oxidative stress markers, and sperm DNA damage in men with idiopathic oligoasthenoteratospermia. Clinical and Experimental Reproductive Medicine. 2021;48(2):150-155. doi:10.5653/cerm.2020.04084
5. Smits RM, Mackenzie-Proctor R, Yazdani A, et al. Antioxidants for male subfertility. Cochrane Database of Systematic Reviews. 2019;3:CD007411. doi:10.1002/14651858.CD007411.pub4
6. Mongioi L, Calogero AE, Vicari E, et al. The role of carnitine in male infertility. Andrology. 2016;4(5):800-807. doi:10.1111/andr.12191
7. Lafuente R, González-Comadrán M, Solà I, et al. Coenzyme Q10 and male infertility: a meta-analysis. Journal of Assisted Reproduction and Genetics. 2013;30(9):1147-1156. doi:10.1007/s10815-013-0047-5
8. Balercia G, Buldreghini E, Vignini A, et al. Coenzyme Q10 treatment in infertile men with idiopathic asthenozoospermia: a placebo-controlled, double-blind randomized trial. Fertility and Sterility. 2009;91(5):1785-1792. PMID: 18439595
9. Safarinejad MR. Efficacy of coenzyme Q10 on semen parameters, sperm function and reproductive hormones in infertile men. Journal of Urology. 2009;182(1):237-248. doi:10.1016/j.juro.2009.02.121
10. Steiner AZ, Hansen KR, Barnhart KT, et al. The effect of antioxidants on male factor infertility: the MOXI randomized clinical trial. Fertility and Sterility. 2020;113(3):552-560. doi:10.1016/j.fertnstert.2019.11.008

Medical Disclaimer​

This article is for informational purposes only and does not constitute medical advice. The information provided should not be used for diagnosing or treating a health problem or disease. Always consult with a qualified healthcare provider before starting any new supplement regimen, particularly if you have underlying health conditions or are taking medications. Individual responses to supplementation may vary, and the effectiveness of L-carnitine and CoQ10 depends on multiple factors including the underlying cause of subfertility. The ExcelMale forum and its contributors are not responsible for any adverse effects or consequences resulting from the use of any suggestions or information contained in this article.

About ExcelMale

ExcelMale.com is a men's health forum founded by Nelson Vergel with over 24,000 members and more than two decades of community discussions on testosterone replacement therapy, hormone optimization, sexual health, and male fertility. The forum serves as a bridge between clinical research and real-world patient experiences, providing evidence-based information while respecting the lived experiences of men navigating complex health decisions.
Nelson Vergel is the author of "Testosterone: A Man's Guide" and "Beyond Testosterone", comprehensive resources for men seeking to understand and optimize their hormonal health. For more information, visit www.ExcelMale.com.
 

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Lakshman KM, Kaplan B, Travison TG, Basaria S, Knapp PE, Singh AB, LaValley MP, Mazer NA, Bhasin S. The effects of injected testosterone dose and age on the conversion of testosterone to estradiol and dihydrotestosterone in young and older men. J Clin Endocrinol Metab. 2010 Aug;95(8):3955-64.

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