Does Time From Ovulation Trigger To Oocyte Pick-Up Affect Intracytoplasmic Sperm Injection Outcomes? A Multi-Center Single-Blinded Randomized Controlled Trial Comparing 36 and 38 Hour Intervals

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Women who undergo assisted reproduction technology (ART) treatment will be eligible for this study. The goal of this randomized clinical trial is to compare the outcomes of ART treatment between women who have 36 and 38 hours interval between the administration of ovulation trigger (ovulation trigger medication initiates oocyte maturation and makes it possible for the egg to be collected by aspiration, during a procedure called oocyte pick-up, OPU) and OPU. The main questions it aims to answer are, does prolonging the trigger-OPU interval to 38-hours improve: 1. Primarily: •Ratio of metaphase-2 oocytes to total number of follicles 2. Secondarily: * Maturation rate * Fertilization rate * Blastulation rate * Premature ovulation rate * Positive pregnancy test rate * Clinical pregnancy rate * Live birth rate compared to 36-hours interval?

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 42
Healthy Volunteers: f
View:

• To undergo assisted reproductive technology (ART) treatment and planning to undergo embryo transfer procedure within 6 months of oocyte collection

• Female partner to be between 18-42 years old at the time of informed consent

• Both partners to consent to participate in the study and be legally eligible to give consent.

Locations
Other Locations
Turkey
Baskent University
RECRUITING
Adana
Ankara University
RECRUITING
Ankara
Hacettepe University
RECRUITING
Ankara
Uludag University
RECRUITING
Bursa
Bahceci Fulya IVF Centre
RECRUITING
Istanbul
Koc University
RECRUITING
Istanbul
VKF American Hospital
RECRUITING
Istanbul
Contact Information
Primary
Engin Turkgeldi, Assoc.Prof.
engtur@gmail.com
00908502508250
Time Frame
Start Date: 2023-04-27
Estimated Completion Date: 2025-12
Participants
Target number of participants: 850
Treatments
Active_comparator: 36-Hour Group
The women randomized to this group will undergo oocyte pick-up procedure 36 hours after the injection of the ovulation triggering agent.~The choice for ovulation trigger agent is at the discretion of the treating physician. The intervention is not the drug but the interval.
Experimental: 38-Hour Group
The women randomized to this group will undergo oocyte pick-up procedure 38 hours after the injection of the ovulation triggering agent.~The choice for ovulation trigger agent is at the discretion of the treating physician. The intervention is not the drug but the interval.
Related Therapeutic Areas
Sponsors
Collaborators: Turkish Society of Reproductive Medicine
Leads: Koç University

This content was sourced from clinicaltrials.gov