Could two hormones beat one for IVF success?
NCT ID NCT07269392
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether giving two hormones (HCG and GnRH agonist) together before transferring a frozen embryo can improve implantation rates. About 170 women aged 24-45 undergoing modified natural cycle frozen embryo transfer will be randomly assigned to receive either the standard HCG trigger or the dual trigger. The main goal is to see if more embryos successfully implant with the dual trigger.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- GnRH agonist (added to HCG for ovulation trigger)
- What this could lead to
- If it works, this could improve the chance of embryo implantation in frozen embryo transfer cycles, potentially increasing pregnancy rates.
- What could go wrong
- This is a Phase 4 trial with only 170 participants, so results may not apply to all IVF patients. The dual trigger may not improve outcomes and could cause side effects.
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
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 170 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 to 44 years
- Sex
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Female participants only
- Healthy volunteers
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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\. 24\<= Age \< 45 patient undergo mNC-FET Exclusion Criteria: 1\. Congenital or acquired uterine abnormalities (uterine malformation, submucosal myoma, intrauterine adhesion or endometrial polyp \>1cm)
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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- Cervical mucus may hold key to better IVF timing
- New embryo transfer device aims to boost IVF success