RECRUITING

GnRH for Luteal Support in IVF/ICSI/FET Cycles

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

During IVF cycles an embryo is generally placed into the uterine cavity between 3 and 5 days after fertilization. For a successful pregnancy to take place, that embryo must then implant in the properly primed and staged endometrium, which subsequently must continue to develop to accommodate the growing and maturing embryo and then fetus. This process is normally regulated by hormonal interactions between the fetal, endometrial and luteal tissue. It has been found that after IVF additional support for the endometrium with progesterone improves implantation and subsequent live birth rates in IVF cycle . Recent data has shown that additional supplementation with a single administration of a GnRH agonist around the time the time of embryo transfer may further enhance these rates .

Official Title

GnRH for Luteal Support in IVF/ICSI/FET Cycles

Quick Facts

Study Start:2015-11
Study Completion:2025-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT02357654

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 40 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * women undergoing IVF/ICSI or frozen embryo transfers (FET) that less than 40 years old.
  1. * day 3 transfers

Contacts and Locations

Study Contact

Peter G McGovern, MD
CONTACT
201-288-6330
mcgovepg@gmail.com

Principal Investigator

Peter G McGovern, MD
PRINCIPAL_INVESTIGATOR
Rutgers University

Study Locations (Sites)

University Reproductive Associates
Hasbrouck Heights, New Jersey, 07604
United States

Collaborators and Investigators

Sponsor: University Reproductive Associates

  • Peter G McGovern, MD, PRINCIPAL_INVESTIGATOR, Rutgers University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2015-11
Study Completion Date2025-03

Study Record Updates

Study Start Date2015-11
Study Completion Date2025-03

Terms related to this study

Additional Relevant MeSH Terms

  • Infertility