FIT-PLESE: A study for overweight women with unexplained infertility, seeking pregnancy report Trial 3
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- STATUS
- Recruiting
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- participants needed
- 90
Summary
FIT-PLESE is a research study to find out the effects of lifestyle modification in obese women with unexplained infertility. Eligible participants will be randomized to either an Intensive Lifestyle Modification Program or a Standard Physical Activity Program for 16 weeks, followed by fertility treatment with ovarian stimulation and intrauterine insemination.
Description
The FIT-PLESE study includes three phases: lifestyle intervention, infertility treatment, and pregnancy. Phase I will involve randomization to either an Intensive Lifestyle Modification program or a Standard Physical Activity Program. The Intensive Lifestyle Modification Program will consist of an over the counter weight loss drug (Orlistat/Alli), caloric restriction assisted by the use of meal replacements (Nutrisystem), and increased physical activity (monitored by a Fitbit). The Standard Physical Activity Program will consist of increased physical activity alone (monitored by a Fitbit). After completion of the 16 week lifestyle intervention, subjects will receive up to 3 cycles of ovarian stimulation with an oral medication (clomiphene citrate), triggered ovulation with hCG, and a single intrauterine insemination per cycle (Phase II). Subjects who conceive in either Phase I or Phase II will have visits once per trimester and all pregnancies will be followed to completion (Phase III). Participation in this study may take up to 18 months to complete, and may require an average of 17 study-related visits.
Details
Condition | Female Infertility |
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Age | 18years - 40years |
Clinical Study Identifier | TX1037 |
Last Modified on | 25 April 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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