Main
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Note: This record shows only 22 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. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT00844350 |
Date of registration:
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13/02/2009 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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The Effect of Oxytocin (OT) and Oxytocin Plus Human Chorionic Gonadotropin (hCG), in Cycles Induced by Letrozole or Clomiphene Citrate
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Scientific title:
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Date of first enrolment:
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October 2006 |
Target sample size:
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177 |
Recruitment status: |
Completed |
URL:
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http://clinicaltrials.gov/show/NCT00844350 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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Phase 2
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Key inclusion & exclusion criteria
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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
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Health Condition(s) or Problem(s) studied
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Ovarian Response
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Intervention(s)
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Drug: letrozole , oxytocin,hCG,clomiphene citrate
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Primary Outcome(s)
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number of follicles, endometrial thickness, and clinical pregnancy rate
[Time Frame: first ,second and third month]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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