Hydrogel implant could offer reversible male contraception
NCT ID NCT05134428
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a new device called the ADAM System, a hydrogel implant placed in the sperm-carrying tubes to block sperm. It was tested in 25 healthy men to see if it is safe and works as a non-permanent form of male birth control. The implant is designed to be reversible, unlike a standard vasectomy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hydrogel implant (ADAM System)
- What this could lead to
- If successful, this could provide a long-lasting but reversible male contraceptive option, similar to a vasectomy but without permanent effects.
- What could go wrong
- This is a small, early feasibility study with only 25 men. The implant may not reliably block sperm, could cause side effects, or may not be easily reversible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
25 people
The number who actually took part.
- Started
-
May 2022
- Finished
-
Mar 2026
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
25 to 65 years
- Sex
-
Male participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. The subject is male 2. Subject is 25 to 65 years of age 3. Subject has a normal semen analysis (≥ 15 million sperm/mL, ≥40% total motility) defined by the WHO Laboratory Manual for the Examination and Processing of Human Semen (5th Edition), based on the average of two semen samples ≥2 days and ≤7 days apart 4. Subject is suitable to undergo a vasectomy as a long-term form of contraception 5. Subject is legally competent 6. In the opinion of the Investigator, the subject is willing and able to comply with the protocol, return for all follow-up visits and complete all protocol assessments, which includes providing recurring semen samples 7. Subject agrees to use an alternative method of contraception with any female partner of reproductive age during the course of the study treatment until study exit occurs 8. Subject is willing to accept an unknown risk of conceiving a pregnancy during the duration of the study. 9. The subject has been informed of the nature of the study, agrees to its provisions, and has willingly provided written informed consent, approved by the appropriate Human Research Ethics Committee (HREC) Exclusion Criteria: * Potential subjects will be excluded if ANY of the following criteria apply: 1. Subject is participating in another interventional clinical trial currently or within the past 3 months from the time of screening 2. Subject has history of prior hormonal therapy use (e.g., androgenic steroids, GnRH agonists and antagonists) within the past 6 months 3. Subject on exam has any of the following: vas not present, abnormal scrotum, large varicocele, hydrocele, filariasis or elephantiasis of scrotum, or intrascrotal mass that would make the subject not suitable for the study 4. Subject has allergic reaction to polyethylene glycol (PEG) containing products or has had a prior severe allergic response to injectable or implantable devices 5. Subject has local genital infections such as balanitis, scrotal skin infection, epididymitis, or orchitis, or tender (inflamed) tip of the penis, but may be admitted after resolution of an acute infection 6. Subject has current coagulopathy or other bleeding disorders 7. Subject currently taking or planning to take any type of systemic medication which could affect sperm count or ejaculation (e.g., anabolic steroids, chemotherapy, alpha blocker) 8. Subject had a previous successful or unsuccessful vasectomy or vasectomy reversal 9. Subject has any clinically significant abnormal findings or other findings identified by Investigator that would exclude the subject.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Healthy male adults are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
AndroUrology
Brisbane, Queensland, 4001, Australia
-
Epworth HealthCare
East Melbourne, Victoria, 3002, Australia
-
South Coast Urology
Wollongong, New South Wales, 2500, Australia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New drug AJ201: does food change how it works?
- Male birth control pill enters human testing
- Hormone gel transfer: does washing or clothing protect women?
- New male birth control pill could work in minutes
- New male contraceptive device aims to be reversible
- Male birth control pill moves closer to reality