Intrauterine Insemination Clinical Trial
Official title:
Effect of GnRH Agonist Administration at the Time of Implantation in Intrauterine Insemination Cycles: A Randomized Controlled Trial
The aim of this study is to assess whether GnRH agonist administration in the luteal phase improves pregnancy outcome in intrauterine insemination (IUI) cycles.
Status | Completed |
Enrollment | 0 |
Est. completion date | December 2007 |
Est. primary completion date | December 2007 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 38 Years |
Eligibility |
Inclusion Criteria: - Women < 38 years old - Bilateral tubal patency confirmed by hysterosonography - Normal ultrasound scan of uterus and ovaries - Normal day 3 basal hormones - Motile sperm count after capacitation = 3 mill/ml Exclusion Criteria: - Endometriosis - Polycystic ovary syndrome - Uterine disease (polyps, myomas and müllerian diseases) |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind
Country | Name | City | State |
---|---|---|---|
Spain | Instituto Valenciano de Infertilidad Spain | Valencia |
Lead Sponsor | Collaborator |
---|---|
Instituto Valenciano de Infertilidad, IVI VALENCIA |
Spain,
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