Could a simple supplement boost IVF success?
NCT ID NCT07783399
First seen Aug 24, 2026 · Last updated Aug 25, 2026 · Updated 1 time
Summary
This trial tests whether taking L-carnitine, a natural supplement, for 12 weeks before egg retrieval can improve the number and quality of eggs and embryos in women undergoing IVF. Researchers will compare women who take the supplement with those who do not, to see if it leads to higher pregnancy rates. The study aims to answer whether this simple addition could make IVF more effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- L-carnitine (500 mg daily for 12 weeks before egg retrieval)
- What this could lead to
- If effective, L-carnitine could become a simple, low-cost supplement to improve IVF success rates by boosting egg and embryo quality.
- What could go wrong
- This is a small, early-stage trial, and results may not apply to all women. Supplements can have side effects, and there is no guarantee of improved pregnancy outcomes.
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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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
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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Sep 2026
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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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * women undergoing IVF process * women aged 18-45 years Exclusion Criteria: * obesity * severe kidney disease * liver insufficiency * endocrine disorders * the use of immunosuppressive medications
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Conditions
The condition(s) this trial relates to.
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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Clinic for Gynecology and Obstetrics Narodni Front
RECRUITINGBelgrade, Savski Venac, 11000, Serbia
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Other studies related to the condition(s) this trial covers.
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- Can a slight dose change boost IVF embryo success?
- Could a cheaper hormone make IVF more affordable?
- Can tiny electric acupuncture needles help women with low egg reserve conceive?