TTrialPathMatch Me to Trials
← Back to trials
RecruitingPolycystic Ovary Syndrome

IVM With Low Cost Priming, Enhanced Oocyte Recovery, and Delayed Transfer

Eligible age

18–38 yrs

Accepts

Women

Locations

1 state

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

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 patient have a PCO pattern in their ovaries during transvaginal ultrasound.

Sponsor: Bruce Rose, MD

You may qualify if…

  • PCO pattern with \> 25 antral follicles
  • AMH \> 3.5

You may not qualify if…

  • BMI \> 35
  • body morphology making transvaginal retrieval difficult or impossible
  • complicating medical condition making pregnancy or IVF relatively contra-indicated

Where it's recruiting

Florida

Jacksonville

Source: ClinicalTrials.gov · NCT04149496 · last updated 2019-11-04

IVM With Low Cost Priming, Enhanced Oocyte Recovery, and Delayed Trans · TrialPath