One shot instead of many: a simpler path to IVF egg retrieval?
NCT ID NCT06635538
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
This pilot study tests a streamlined ovarian stimulation protocol for women undergoing fertility treatment. Participants receive a single injection of corifollitropin alfa plus daily oral clomiphene citrate, instead of the usual multiple daily injections. Researchers will measure hormone levels and egg retrieval outcomes to see if this simpler approach works as well as standard protocols.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A single injection of corifollitropin alfa plus daily oral clomiphene citrate
- What this could lead to
- If this works, it could simplify ovarian stimulation for IVF, reducing the number of injections women need while maintaining good egg retrieval outcomes.
- What could go wrong
- This is a small pilot study with only 20 participants, so results may not apply broadly. The approach might not produce enough eggs or could cause hormone imbalances.
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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20 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Nov 2025
- 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 40 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: Age \<= 40 AMH (Anti-Mullerian Hormone) 1.2-3.5 ng/ml or AFC 7-20 No family history of hereditary or chromosomal diseases Body mass index (BMI) 18 to 30 kg/m2
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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.
Contacts and locations
Locations
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Departamento de Ginecología Obstetricia y Reproducción. Hospital Universitari Dexeus
Barcelona, 08037, Spain
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Dexeus Mujer Sabadell
Sabadell, Barcelona, 08203, Spain
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Dexeus Mujer Sant Cugat
Sant Cugat del Vallès, Barcelona, 08195, Spain
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