IVF debate: does less stimulation mean better embryos?
NCT ID NCT04983173
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looked at 110 women aged 35-40 with low ovarian reserve undergoing IVF. Half received a mild stimulation (clomiphene plus low-dose hormones) and half received a stronger stimulation (higher-dose hormones). The goal was to see which approach led to more good-quality blastocysts. Researchers also tracked hormone changes and egg counts to understand how stimulation intensity affects early embryo development.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Clomiphene citrate and recombinant follicle-stimulating hormone (rFSH)
- What this could lead to
- If successful, this could help doctors choose the best stimulation intensity for IVF patients with low ovarian reserve, potentially improving embryo quality.
- What could go wrong
- This is a small, completed Phase 4 trial with only 110 participants. Results may not apply to all infertility patients, and the study focuses on embryo quality, not live birth rates.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
110 people
The number who actually took part.
- Started
-
Nov 2021
- Finished
-
Mar 2026
- Lead sponsor
-
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
-
35 to 40 years
- Sex
-
Female participants only
- Healthy volunteers
-
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: * Able and willing to sign the Patient Consent Form and adhere to study visitation schedule * Antral follicle count (AFC) ≥ 5 and ≤ 10 * Anti-Mullerian hormone (AMH) ≤1.5 ng/ml (AMH result of up to one year will be valid) * Age ≥ 35 years and ≤40 years * BMI ≥18.5 and \<25 kg/m2 Exclusion Criteria: * AFC \>10 * History of untreated autoimmune, endocrine or metabolic disorders * Contraindication for hormonal treatment * Preimplantation genetic diagnosis cycles * Severe male factor (sperm concentration \<5 M/mL) * Recent history of severe disease requiring regular treatment (clinically significant concurrent medical condition that could compromise subject safety or interfered with the trial assessment and patients with any contraindication of being pregnant).
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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
-
Salud de la Mujer Dexeus
Barcelona, 08028, Spain
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Other studies related to the condition(s) this trial covers.
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