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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00700492
Other study ID # ML2437-30/12/2003
Secondary ID
Status Terminated
Phase N/A
First received June 17, 2008
Last updated June 24, 2015
Start date May 2004
Est. completion date June 2008

Study information

Verified date June 2015
Source University Hospital, Gasthuisberg
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

A randomized study to investigate if hormonal luteal support after intra-uterine insemination (IUI) in ovulation induction cycles with human menopausal gonadotropin increases the pregnancy rate


Recruitment information / eligibility

Status Terminated
Enrollment 82
Est. completion date June 2008
Est. primary completion date March 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 43 Years
Eligibility Inclusion Criteria:

- Signed informed consent

- Tubal patency demonstrated

- ovulation induction with human menopausal gonadotropin

Exclusion Criteria:

- ovulation induction with clomiphene citrate

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
progesterone
vaginal capsules 3X200mg daily

Locations

Country Name City State
Belgium Leuven University Fertility Center Leuven Vlaams Brabant

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Gasthuisberg

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical pregnancy rate per cycle 12 weeks pregnancy No
Secondary rate of miscarriages per cycle 12 weeks pregnancy No
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