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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Last refreshed on: 17 October 2012
Main ID:  NCT00844350
Date of registration: 13/02/2009
Primary sponsor: Tabriz University
Public title: The Effect of Oxytocin (OT) and Oxytocin Plus Human Chorionic Gonadotropin (hCG), in Cycles Induced by Letrozole or Clomiphene Citrate
Scientific title:
Date of first enrolment: October 2006
Target sample size: 177
Recruitment status: Completed
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment  
Countries of recruitment
Key inclusion & exclusion criteria

Inclusion Criteria:

- infertile women who had chronic anovulation

- classical PCOS with CC+hCG failure

- age <40 y

- had patent tubes on hysterosalpingography

- no other pelvic pathology

- participated in this study

Exclusion Criteria:

- hypersensitivity to any oxytocic medications

- history of cardiovascular disease

- took anti-hypertensive medications were excluded.

- women with blood pressure less than 90/60 mmHg

- abnormal spermogram

- anxiety

- excess prolactin levels

- other causes of infertility were excluded

Age minimum: 17 Years
Age maximum: 40 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Ovarian Response
Drug: letrozole , oxytocin,hCG,clomiphene citrate
Primary Outcome(s)
number of follicles, endometrial thickness, and clinical pregnancy rate [Time Frame: first ,second and third month]
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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