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Sponsored by: |
University of Connecticut Health Center |
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Information provided by: | University of Connecticut |
ClinicalTrials.gov Identifier: | NCT00633555 |
Patients who have undergone in vitro fertilization (IVF) and produced four or less follicles or had four or less oocytes (eggs) retrieved are often referred to as poor responders. We will refer to these patients from this point forward as "low responders" to avoid using a potentially offensive label. We are currently using 2 different IVF medication protocols in our practice to treat low responder patients with infertility: the "Microdose Leuprolide" protocol and the "Luteal Phase Ganirelix" protocol. We would like to conduct a randomized-controlled trial and randomize patients to one treatment group or the other to determine which medication protocol is more effective in treating infertility in this group of patients.
Condition |
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Infertility |
Study Type: | Observational |
Study Design: | Case Control, Prospective |
Official Title: | A Randomized Controlled Trial of Microdose Leuprolide Protocol vs. Luteal Phase Ganirelix Protocol in Predicted Low Responders |
Estimated Enrollment: | 240 |
Study Start Date: | July 2006 |
Estimated Study Completion Date: | September 2009 |
Estimated Primary Completion Date: | September 2009 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 21 Years to 44 Years |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Women ages 21-44 who are currently undergoing In Vitro Fertilization treatment at our center.
Inclusion Criteria:
OR
Exclusion Criteria:
Contact: Victoria L Scranton, BS | 860-679-4612 | vscranton@nso2.uchc.edu |
United States, Connecticut | |
The Center for Advanced Reproductive Services | Recruiting |
Farmington, Connecticut, United States, 06030-6224 |
Principal Investigator: | John Nulsen, MD | The Center for Advanced Reproductive Services, P.C. |
Responsible Party: | The Center for Advanced Reproductive Services ( John Nulsen, MD ) |
Study ID Numbers: | 06-198-2, CARS-06-198 |
Study First Received: | March 4, 2008 |
Last Updated: | December 9, 2008 |
ClinicalTrials.gov Identifier: | NCT00633555 History of Changes |
Health Authority: | United States: Institutional Review Board |
Genital Diseases, Female Infertility Ganirelix Leuprolide Genital Diseases, Male |
Genital Diseases, Female Infertility Genital Diseases, Male |