PACTR202105631565416
Recruiting
未知
A RANDOMISED CONTROLLED COMPARISON OF VAGINAL AND ORAL BROMOCRIPTINE IN THE MANAGEMENT OF HYPERPROLACTINEMIA AMONG WOMEN ATTENDING INFERTILITY CLINIC IN ABUTH.
Irshad Asma0 sites64 target enrollmentApril 19, 2021
ConditionsFertility-female
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Fertility-female
- Sponsor
- Irshad Asma
- Enrollment
- 64
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •This will include consenting and well\-motivated infertile women with laboratory evidence of hyperprolactinemia who are ready to comply with study requirements (clinic visits, repeated blood collections, vaginal drug administrations and timely use of medications).
Exclusion Criteria
- •Women with space occupying lesions or other complications requiring urgent intervention, those with active genital tract infections or cancers, renal or hepatic insufficiency, those already on treatment at the time of the study, nonconsenting women and those with allergies to any component of the drugs will be excluded from the study.
Outcomes
Primary Outcomes
Not specified
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