跳至主要内容
临床试验/CTRI/2022/11/047112
CTRI/2022/11/047112尚未招募不适用

Effect of Remote Ischemic Pre-conditioning (RIPC) on Endothelial Dysfunction in Women with Polycystic Ovary Syndrome(PCOS)

Institute of medical sciences1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年10月11日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
maximum percentage increase in flow after cuff deflation compared to baseline flow

研究概览

简要总结

We are conducting an explorative, randomized, double- blinded, SHAM- controlled trial at the outpatient clinic at the department of Gynaecology in collaboration with the Departments of Cardiology, Endocrinology and Radiology at IMS, BHU, Varanasi.

We will include 50 pre- menopausal women with classical PCOS fulfilling the inclusion and exclusion criteria as described earlier.

The patients will be randomly assigned 1:1 to RIPC (Remote Ischemic Pre- Conditioning) or SHAM group using block method once daily for 7 days . Outcome variables as described will be measured at baseline and RIPC.

The intervention group will recieve a RIPC protocol of 4 cycles of 5 minutes each with occlusion to 220 mmHg with standard sphymomanometer BP cuff on the right arm followed by 5 minutes re-perfusion . One intervention of 4 cycles amounting to 35 minutes will be performed daily for 7 days.

The SHAM procedure will consist of a pressure cuff , inflated on the right upper arm for the same periods as the RIPC intervention but only to 40 mmHg as it has shown to mimic occlusion but not limiting blood flow.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • Case known of classical PCOS.

排除标准

  • Thyroid dysfunction Cushing syndrome Late onset of congenital adrenal hyperplasia Pregnancy and breastfeeding Use of glucocorticoids, OCPs, ovulatory agents within 3 months of study Smoking, drug and alcohol abuse.

结局指标

主要结局

maximum percentage increase in flow after cuff deflation compared to baseline flow

时间窗: 4 cycles of 5 minutes each with occlusion to 220 mmHg followed by 5 min re- perfusion | another intervention of 4 cycles of 35 minutes daily for 7 days

次要结局

未报告次要终点

研究者

发起方
Institute of medical sciences
申办方类型
Government medical college

研究点 (1)

Loading locations...

相似试验