IVM With Low Cost Priming, Enhanced Oocyte Recovery, and Delayed Transfer
Recruiting
N/A
Interventional Study
Polycystic Ovary Syndrome
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 38
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 300 (estimated)
- Sponsor
- Bruce Rose, MD · Other
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About This Trial
A protocol was developed to improve pregnancy results after IVM compared to results from studies in the literature. Differences from most published protocols include the use of the Steiner-Tan needle to optimize oocyte environment during oocyte retrieval, use of oral medications and very low doses of FSH, and delayed embryo transfer during subsequent warmed cryo-preserved embryo transfer. Eligible…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* PCO pattern with \> 25 antral follicles
* AMH \> 3.5
Exclusion Criteria:
* BMI \> 35
* body morphology making transvaginal retrieval difficult or impossible
* complicating medical condition making pregnancy or IVF relatively contra-indicated
Contacts