The goal of this clinical trial is to evaluate a long Clomid protocol as compared to a 5-day Clomid protocol for ovarian stimulation in patients with diminished ovarian reserve undergoing ovarian stimulation for in-vitro fertilization. The aim of the long Clomid protocol is to intensify stimulation of the ovaries and reduce both cost and injection burden for patients. Participants will be randomized to receive the long Clomid protocol vs. the typical protocol involving Clomid only for 5 days followed by growth hormone-releasing hormone (GnRH) antagonist. The primary outcome the investigators will evaluate will be the number of mature eggs retrieved.
Undergoing IVF
Must meet POSEIDON criteria based on clinic evaluation
Female partner: Antral follicle count of 2 or more and age <45 at time of stimulation start
Male partner/sperm source: Cannot be azoospermic
Normal ovarian reserve or good response
Allergy or adverse reaction to Clomid
Minimal stimulation protocols
History of prior premature ovulation