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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03044756
Other study ID # Omit
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received February 1, 2017
Last updated February 6, 2017
Start date January 1, 2017
Est. completion date December 30, 2017

Study information

Verified date February 2017
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Omitting the GnRH antagonist on the day of the trigger can be cost effective and more convenient to the women. We will study the impact of omitting the antagonist dose in a prospective randomized trial


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 30, 2017
Est. primary completion date August 30, 2017
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- All antagonist cycle ivf who agree to participate

Exclusion Criteria:

- expected poor responders.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Omit Citrotide 0.25 dose on the day of triggering of ovulation
Omit Citrotide 0.25 dose on the day of triggering of ovulation

Locations

Country Name City State
Egypt Osama Abdalmageed Assiut Non-US/Non-Canadian
Egypt Osama Abdalmageed Assiut Non-US/Non-Canadian

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Chang HJ, Lee JR, Jee BC, Suh CS, Lee WD, Kim SH. Cessation of gonadotropin-releasing hormone antagonist on triggering day in flexible multiple-dose protocol: A randomized controlled study. Clin Exp Reprod Med. 2013 Jun;40(2):83-9. doi: 10.5653/cerm.2013.40.2.83. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of retrieved oocytes total number and maturation of the retrieved oocytes One Month