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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00740025
Other study ID # 1-Sharara
Secondary ID
Status Completed
Phase N/A
First received August 21, 2008
Last updated October 12, 2010
Start date January 2006
Est. completion date January 2010

Study information

Verified date October 2010
Source Virginia Center for Reproductive Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This is a prospective randomized study evaluating dosing frequency of gonadotropin administration in ART cycles.


Description:

Using once daily or bid dosing of gonadotropins in ART has been arbitrary with no studies showing whether splitting the medication dose improves ART parameters. This study was undertaken to provide an answer to this important question.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date January 2010
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Female
Age group 21 Years to 39 Years
Eligibility Inclusion Criteria:

- women < 40 undergoing ART

Exclusion Criteria:

- women > 40

- endometriomas

- severe cervical stenosis

- testicular sperm

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Virginia Center for Reproductive Medicine Reston Virginia

Sponsors (1)

Lead Sponsor Collaborator
Virginia Center for Reproductive Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ongoing pregnancy 1 year No
Secondary peak estradiol, number of follicles, number of oocytes, implantation rate, multiple pregnancy rate 1 year No
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