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NCT01933009 Clinical Trial

The Effect of GnRH Administration During Luteal Support in Frozen-thawed Transfer Cycles

Pregnancy Rate Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01933009
Other study ID # 79/13
Secondary ID
Status Recruiting
Phase N/A
First received August 28, 2013
Last updated August 28, 2013
Start date August 2013
Est. completion date August 2014

Study information
Verified date August 2013
Source Assaf-Harofeh Medical Center
Contact Ido Ben-Ami, MD PhD
Phone 972-8-9779005
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Observational [Patient Registry]

Clinical Trial Summary

GnRH administration during the luteal phase was found to significantly increase pregnancy rates in women undergoing fresh-cycle IVF cycles.

We aim to investigate the effect of GnRH administration during the luteal phase in women undergoing frozen-thawed IVF cycles.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date August 2014
Est. primary completion date May 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

Frozen-thawed IVF cycles

Exclusion Criteria:

Hydrosalpings Uterine myomas

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Israel IVF and infertility unit, Assaf Harofeh Medical Center Zerifin Be'er-Ya'akov

Sponsors (1)
Lead Sponsor Collaborator
Assaf-Harofeh Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pregnancy rate 1 year No
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