Sperm DNA FragmentationPhase 1NCT07873502
HMG Treatment Reduces Sperm DNA Fragmentation
A Phase 1 study testing Human Menopausal Gonadotropin (hMG) and Vitamin E in people with Sperm DNA Fragmentation, run by Jinling Hospital, China at 1 site in China.
Trial summary
Male factors account for approximately 50% of infertility cases. The principal etiologies of male infertility include sexual dysfunction, semen abnormalities arising from various etiologies, and idiopathic infertility. Read more about this study
- Who is it for?
- Ages 21 years and older, men only
- Conditions the study is for
- Sperm DNA Fragmentation
- What is being tested?
- Human Menopausal Gonadotropin (hMG) and Vitamin E
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 114 participants
- Where
- 1 siteChina
- Study dates
- 2 Jul 2025to 31 Aug 2026
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 21 years and older
- Men only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- (1) couple has cohabited for over 12 months, maintained regular unprotected intercourse, yet the woman remains infertile.; (2) DFI > 30% 19on two or more semen analyses performed under standard testing conditions, with at least 7 days between tests; (3) serum sex hormone levels within the normal reference ranges: testosterone 9.4-37.0 nmol/L, follicle-stimulating hormone (FSH) 1.2-5.5 IU/L, luteinizing hormone (LH) 1.3-6.3 IU/L, and inhibin B 18.22-311.27 ng/L
Who cannot join
- (1) Allergy to any component of the study medication; (2) Pituitary or hypothalamic tumors; (3) Decompensated thyroid disease, adrenal insufficiency, or hyperprolactinemia; (4) Prostate cancer, testicular tumors, or androgen-dependent tumors; (5) Primary testicular failure; (6) Chromosomal or genetic abnormalities; (7) History of thrombosis; (8) Currently participating in another clinical trial, or any condition that in the investigator's judgment could interfere with participation or assessment.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Human Menopausal Gonadotropin Treatment for Sperm DNA Fragmentation in Men With Idiopathic Infertility: A Prospective Controlled Study
Male factors account for approximately 50% of infertility cases. The principal etiologies of male infertility include sexual dysfunction, semen abnormalities arising from various etiologies, and idiopathic infertility. Semen analysis remains a key method for assessing male fertility, with semen abnormalities representing the most significant contributing factors. Common semen abnormalities include oligozoospermia, asthenozoospermia, and teratozoospermia. In recent years, elevated sperm DNA fragmentation (SDF) has emerged as an important and increasingly prevalent cause of male infertility. The World Health Organization (WHO) Laboratory Manual for the Examination and Processing of Human Semen, Sixth Edition, likewise emphasizes the importance of sperm DNA integrity, presents several techniques, and outlines the role of SDF testing in male infertility In infertile couples, the male sperm DFI is significantly higher than that of men with normal fertility (24.5% vs 17%), and the proportion of DFI > 30% among men in infertile couples is greater. DFI is significantly associated with recurrent pregnancy loss. A meta-analysis shows that SDF is associated with sporadic miscarriage. Recent animal studies indicate that SDF may lead to fragmentation and random distribution of paternal chromosomal segments in the developing embryo, resulting in mosaicism of different genotypes within cells. Collectively, these findings suggest that increased SDF may elevate the risk of embryonic abnormalities. In IUI cycles, low SDF is associated with higher clinical pregnancy and live birth rates. IVF-ET studies indicate a significant association between high SDF and poorer embryo quality. The clinical pregnancy rate in the higher sperm DFI group is significantly lower than that in the low-DFI group.
Follicle-stimulating hormone (FSH) plays a well-established role in human spermatogenesis. In most cases of azoospermia due to hypogonadotropic hypogonadism (HH), spermatogenesis can be effectively initiated. For patients with oligoasthenoteratospermia (OAT) who have low FSH levels, FSH may be administered at the same dose used for HH, enabling these infertile men to benefit from gonadotropin-based therapy. However, in some countries, FSH is not approved for male infertility treatment. Several clinical trials have evaluated recombinant FSH therapy in men with primary infertility, showing significant improvements in sperm concentration but little or no effect on progressive motility. However, most previous studies focused on men with oligoasthenoteratozoospermia or hypogonadotropic hypogonadism. It remains unclear whether HMG therapy benefits infertile men with isolated DFI elevation but normal conventional sperm count and normal sex hormone levels. This patient subgroup represents a clinical dilemma, as treatment options are limited. Therefore, we conducted this trial to evaluate the efficacy of HMG in improving DFI in this specific population.
This study aims to evaluate the efficacy of HMG treatment on sperm DFI and conventional parameters, sex hormone levels, and seminal plasma biochemical markers in infertile men with abnormal sperm DFI through a prospective controlled design.
- Conditions
- Sperm DNA Fragmentation
- Being tested
- Human Menopausal Gonadotropin (hMG), Vitamin E
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Human Menopausal Gonadotropin (hMG)Drug
Human Menopausal Gonadotropin(HMG), is a hormone medicine made from the urine of women after menopause. It contains two hormones: FSH and LH.
Vitamin EDrug
Vitamin E is a fat-soluble nutrient that acts as an antioxidant in the body. It helps protect cells from damage caused by free radicals, supports immune function, and helps keep skin and eyes healthy.
| Study group | Role | What they receive |
|---|---|---|
| Experimental Arm | Experimental | Not described Receives: Drug: Human Menopausal Gonadotropin (hMG) |
| Control Arm | Active comparator | Not described Receives: Drug: Vitamin E |
What is being measured
The primary outcome is the main question the study is designed to answer.
sperm DFI
Sperm DFI (DNA Fragmentation Index) is the percentage of sperm in a semen sample that have broken or damaged DNA.
Measured: From enrollment to the end of treatment at 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Oct 2026
- Study start2 Jul 2025
- Primary completion10 Oct 2025
- Study completion31 Aug 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Sperm DNA FragmentationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 114 participants (actual)
Sponsor and investigators
- Lead sponsor
- Jinling Hospital, China
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Bing Yao, Jinling Hospital, China
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07873502
- Sponsor's protocol ID
- HMG treatment for SDF
- Status last verified
- Oct 2026
- First submitted
- 1 Oct 2026
- Last updated
- 14 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 14 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Human Menopausal Gonadotropin Treatment for Sperm DNA Fragmentation in Men With Idiopathic Infertility: A Prospective Controlled Study
- ClinicalTrials.gov ID
- NCT07873502
- Acronym / sponsor ID
- HMG treatment for SDF
- Conditions
- Sperm DNA Fragmentation
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 114 participants (actual)
- Lead sponsor
- Jinling Hospital, ChinaUniversity, hospital or other
- Study start
- 2 Jul 2025 (actual)
- Primary completion
- 10 Oct 2025 (actual)
- Study completion
- 31 Aug 2026 (actual)
- First posted
- 14 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Male factors account for approximately 50% of infertility cases. The principal etiologies of male infertility include sexual dysfunction, semen abnormalities arising from various etiologies, and idiopathic infertility. Semen analysis remains a key method for assessing male fertility, with semen abnormalities representing the most significant contributing factors. Common semen abnormalities include oligozoospermia, asthenozoospermia, and teratozoospermia. In recent years, elevated sperm DNA fragmentation (SDF) has emerged as an important and increasingly prevalent cause of male infertility. The World Health Organization (WHO) Laboratory Manual for the Examination and Processing of Human Semen, Sixth Edition, likewise emphasizes the importance of sperm DNA integrity, presents several techniques, and outlines the role of SDF testing in male infertility In infertile couples, the male sperm DFI is significantly higher than that of men with normal fertility (24.5% vs 17%), and the proportion of DFI > 30% among men in infertile couples is greater. DFI is significantly associated with recurrent pregnancy loss. A meta-analysis shows that SDF is associated with sporadic miscarriage. Recent animal studies indicate that SDF may lead to fragmentation and random distribution of paternal chromosomal segments in the developing embryo, resulting in mosaicism of different genotypes within cells. Collectively, these findings suggest that increased SDF may elevate the risk of embryonic abnormalities. In IUI cycles, low SDF is associated with higher clinical pregnancy and live birth rates. IVF-ET studies indicate a significant association between high SDF and poorer embryo quality. The clinical pregnancy rate in the higher sperm DFI group is significantly lower than that in the low-DFI group.
Follicle-stimulating hormone (FSH) plays a well-established role in human spermatogenesis. In most cases of azoospermia due to hypogonadotropic hypogonadism (HH), spermatogenesis can be effectively initiated. For patients with oligoasthenoteratospermia (OAT) who have low FSH levels, FSH may be administered at the same dose used for HH, enabling these infertile men to benefit from gonadotropin-based therapy. However, in some countries, FSH is not approved for male infertility treatment. Several clinical trials have evaluated recombinant FSH therapy in men with primary infertility, showing significant improvements in sperm concentration but little or no effect on progressive motility. However, most previous studies focused on men with oligoasthenoteratozoospermia or hypogonadotropic hypogonadism. It remains unclear whether HMG therapy benefits infertile men with isolated DFI elevation but normal conventional sperm count and normal sex hormone levels. This patient subgroup represents a clinical dilemma, as treatment options are limited. Therefore, we conducted this trial to evaluate the efficacy of HMG in improving DFI in this specific population.
This study aims to evaluate the efficacy of HMG treatment on sperm DFI and conventional parameters, sex hormone levels, and seminal plasma biochemical markers in infertile men with abnormal sperm DFI through a prospective controlled design.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Experimental Arm | Experimental | Drug: Human Menopausal Gonadotropin (hMG) |
| Control Arm | Active comparator | Drug: Vitamin E |
Who may qualify
- Ages
- 21 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- (1) couple has cohabited for over 12 months, maintained regular unprotected intercourse, yet the woman remains infertile.; (2) DFI > 30% 19on two or more semen analyses performed under standard testing conditions, with at least 7 days between tests; (3) serum sex hormone levels within the normal reference ranges: testosterone 9.4-37.0 nmol/L, follicle-stimulating hormone (FSH) 1.2-5.5 IU/L, luteinizing hormone (LH) 1.3-6.3 IU/L, and inhibin B 18.22-311.27 ng/L
Key exclusion criteria (1 listed)
- (1) Allergy to any component of the study medication; (2) Pituitary or hypothalamic tumors; (3) Decompensated thyroid disease, adrenal insufficiency, or hyperprolactinemia; (4) Prostate cancer, testicular tumors, or androgen-dependent tumors; (5) Primary testicular failure; (6) Chromosomal or genetic abnormalities; (7) History of thrombosis; (8) Currently participating in another clinical trial, or any condition that in the investigator's judgment could interfere with participation or assessment.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Human Menopausal Gonadotropin (hMG)Human Menopausal Gonadotropin(HMG), is a hormone medicine made from the urine of women after menopause. It contains two hormones: FSH and LH. | Drug | Experimental Arm |
| Vitamin EVitamin E is a fat-soluble nutrient that acts as an antioxidant in the body. It helps protect cells from damage caused by free radicals, supports immune function, and helps keep skin and eyes healthy. | Drug | Control Arm |
Primary outcome
sperm DFI
Time frame: From enrollment to the end of treatment at 3 months
Sperm DFI (DNA Fragmentation Index) is the percentage of sperm in a semen sample that have broken or damaged DNA.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Oct 2026.
- Individual participant dataSharing planned: Yes
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing Human Menopausal Gonadotropin (hMG) and Vitamin E in people with Sperm DNA Fragmentation, run by Jinling Hospital, China at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
sperm DFI (time frame: From enrollment to the end of treatment at 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Oct 2026.