Actively Recruiting
IVM With Low Cost Priming, Enhanced Oocyte Recovery, and Delayed Transfer
Led by Bruce Rose, MD · Updated on 2019-11-04
300
Participants Needed
1
Research Sites
242 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
IVM With Low Cost Priming, Enhanced Oocyte Recovery, and Delayed Transfer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female participants aged 18 to 38 years
- Presence of polycystic ovary (PCO) pattern with more than 25 antral follicles
- Anti-Mullerian hormone (AMH) level greater than 3.5
You will not qualify if you...
- Body mass index (BMI) greater than 35
- Body shape or size making transvaginal oocyte retrieval difficult or impossible
- Medical conditions that make pregnancy or IVF relatively unsafe or contraindicated
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Brown Fertility
Jacksonville, Florida, United States, 32256
Actively Recruiting
Research Team
B
Bruce I Rose, MD, PhD
CONTACT
S
Samuel Brown, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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