跳至主要内容
临床试验/PACTR202105631565416
PACTR202105631565416招募中未知

A RANDOMISED CONTROLLED COMPARISON OF VAGINAL AND ORAL BROMOCRIPTINE IN THE MANAGEMENT OF HYPERPROLACTINEMIA AMONG WOMEN ATTENDING INFERTILITY CLINIC IN ABUTH.

Irshad Asma0 个研究点目标入组 64 人开始时间: 2021年4月19日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
64

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • 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).

排除标准

  • 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.

研究者

发起方
Irshad Asma

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