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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00503217
Other study ID # VLC-JB-0205-307-9
Secondary ID
Status Completed
Phase Phase 4
First received July 17, 2007
Last updated September 5, 2016
Start date February 2005
Est. completion date December 2007

Study information

Verified date September 2016
Source Instituto Valenciano de Infertilidad, IVI VALENCIA
Contact n/a
Is FDA regulated No
Health authority Spain: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of this study is to assess whether GnRH agonist administration in the luteal phase improves pregnancy outcome in intrauterine insemination (IUI) cycles.


Recruitment information / eligibility

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)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind


Related Conditions & MeSH terms


Intervention

Drug:
Tryptorelin


Locations

Country Name City State
Spain Instituto Valenciano de Infertilidad Spain Valencia

Sponsors (1)

Lead Sponsor Collaborator
Instituto Valenciano de Infertilidad, IVI VALENCIA

Country where clinical trial is conducted

Spain, 

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Completed NCT05413629 - The Effect of Web Based Education on the Level of Coping With Infertility Stress and Infertility Self-Efficacy N/A