This study is for women with infertility who are undergoing in-vitro fertilization (IVF) and have diminished ovarian reserve. It compares two ways of using Clomiphene Citrate (Clomid) for ovarian stimulation: a standard 5-day protocol and a longer protocol. Clomid works by helping your body release more follicle-stimulating hormone (FSH), which encourages your ovaries to produce eggs. The longer Clomid protocol aims to stimulate the ovaries more intensely, potentially reducing costs and the number of injections you need. Researchers want to see if the longer Clomid protocol results in a higher number of mature eggs retrieved. You would be randomly assigned to one of the two Clomid groups. To join, you must be a woman between 18 and 45 years old, meet specific criteria for ovarian reserve (POSEIDON criteria), and be planning a 'freeze-all' cycle or a fresh transfer if in the short Clomid group. The study is currently unclear on its recruitment status.

Study design

This is an interventional study planning to enroll 120 women. Participants will be randomly assigned to receive either the long Clomid protocol or the standard 5-day Clomid protocol.

What's involved

Not specified in the trial record.

Compensation

Not stated in the trial record.

Follow-up

The number of mature oocytes will be measured up to 1 month after the study is completed.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.