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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01622023
Other study ID # 1/2012
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date October 2010
Est. completion date June 2013

Study information

Verified date April 2019
Source Universitair Ziekenhuis Brussel
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the present study is to prospectively evaluate whether performing an intra-uterine insemination 24 hours after the spontaneous LH peak may result in significantly higher ongoing pregnancy rates compared to 48 hours.


Recruitment information / eligibility

Status Completed
Enrollment 435
Est. completion date June 2013
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 39 Years
Eligibility Inclusion Criteria:

- below 39 years of age on the day of LH peak

- donor semen

- natural cycle (without CC)

- cycle with less than 3 follicles reaching 15 mm of diameter or more.

- with basal hormonal values of progesterone ( < 1,2 ng/dl)

Exclusion Criteria:

The patients excluded are women

- who underwent more than 6 intrauterine inseminations,

- with tubal infertility

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
intra-uterine insemination
Artificial insemination is the process by which sperm is placed into the reproductive tract of a female for the purpose of impregnating the female by using means other than sexual intercourse or natural insemination.

Locations

Country Name City State
Belgium Christophe Blockeel Brussel

Sponsors (1)

Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary pregnancy rate end of 2013 (up to 2 years)
Secondary live birth rate end of 2013 (up to 2 years)
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