Evaluation of a Long Versus Short Clomid Protocol for Controlled Ovarian Stimulation
Recruiting
Phase 4
Interventional Study
Infertility, Female
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 44
- Sex
- Female
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 120 (estimated)
- Sponsor
- University of Southern California · Other
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About This Trial
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 randomiz…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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
* Planning freeze-all cycle (regardless of blastocyst or cl…
Contacts