临床试验/CTRI/2024/11/076392

CTRI/2024/11/076392尚未招募3 期

A Randomized controlled trial to evaluate the efficacy of Atosiban in patients undergoing Embryo transfer.

Sree Supriya M1 个研究点分布在 1 个国家目标入组 60 人开始时间: 2024年11月12日最近更新: 2024年10月29日

试验速览

阶段: 3 期
状态: 尚未招募
发起方
入组人数: 60
试验地点: 1
主要终点: Biochemical Pregnancy rate

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Women undergoing embryo transfer who fulfil the inclusion criteria are selected and divided into two groups - the first group given the full dose - bolus dose followed by continuous intravenous infusion of 18 mg at the rate of 20 drops/min for an hour and 6 drops/min for next 2 hours and the second group proceeded without Atosiban, . Our primary objective is Biochemical pregnancy rate which is determined by a positive urine pregnancy test or serum hCG> 20 mIU/ml measured 2 weeks after embryo transfer.

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: Participant and Outcome Assessor Blinded

入排标准

年龄范围: 23.00 Year(s) 至 50.00 Year(s)（—）
性别: Female

入选标准

•Previous atleast one implantation failure Adenomyosis.
•by MUSA classification Grade A and B embryos.

排除标准

•Hydrosalpinges on scan and untreated Moderate or severe endometriosis Abnormal Chromosome in either or both partners Fibroids.
•FIGO 0,1,2 Uncorrected septate uterus.

结局指标

主要结局

Biochemical Pregnancy rate

时间窗: 5 weeks

次要结局

Implantation Rate(6 weeks of gestation)

研究者

发起方

Sree Supriya M

申办方类型

Private hospital/clinic

责任方

Principal Investigator

主要研究者

Sree Supriya M

A4 Hospital and Fertility centre

研究点 (1)

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