Isotretinoin vs hCG for Male Infertility

No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This study compares two medical treatments to see how well they improve sperm production in men with infertility due to low sperm counts (oligospermia) or no sperm in the semen due to non-obstructive causes (nonobstructive azoospermia). Some men with these conditions have limited nonsurgical treatment options, and current therapies do not work for everyone.

Participants in this study will be adult men ages 19 to 50 who have been diagnosed with oligospermia or nonobstructive azoospermia and do not have a correctable cause for infertility. Eligible participants will be randomly assigned to receive one of two treatments for three months: oral isotretinoin taken twice daily, or human chorionic gonadotropin (hCG) injections given three times per week. hCG is a standard hormonal therapy used in certain types of male infertility, while isotretinoin is being studied for its potential role in stimulating sperm production.

At the start of the study, participants will have blood tests to measure reproductive hormone levels and a semen analysis. Blood tests will be repeated at one month and three months, and a repeat semen analysis will be performed at three months, which corresponds to a full cycle of sperm development. The main goal of the study is to determine whether motile (moving) sperm appear in the semen after treatment. Additional goals include measuring changes in sperm count and hormone levels, as well as monitoring medication side effects.

Both study medications are FDA-approved and have known side effect profiles. Participants may or may not experience improvement in sperm production. The results of this study may help guide future treatment options for men with infertility due to low or absent sperm production.

Who Is on the Research Team?

CD

Chris Deibert, MD, MPH

Principal Investigator

University of Nebraska

Are You a Good Fit for This Trial?

Inclusion Criteria

Willing and able to comply with study procedures, including laboratory testing, semen analyses, and follow-up visits
No other identified and correctable cause of infertility
Considered appropriate candidates for medical therapy for infertility in the clinical judgment of the investigators
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Exclusion Criteria

I have been successfully treated for infertility with medication.
Significant medical or psychiatric conditions that, in the opinion of the investigators, would interfere with safe participation
Inability to provide semen samples
See 6 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either oral isotretinoin or hCG injections for 3 months to improve sperm production

3 months
Blood tests at baseline, 1 month, and 3 months; semen analysis at 3 months

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Human chorionic gonadotrophin (hCG)
  • Isotretinoin

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Isotretinoin Treatment ArmExperimental Treatment1 Intervention
Group II: hCG Treatment ArmActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Nebraska

Lead Sponsor

Trials
563
Recruited
1,147,000+