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临床试验/NCT07176910
NCT07176910招募中不适用

Doppler Ultrasound-Guided Angiopuncture for Dysmenorrhea Pain: A Clinical Trial

City University of Hong Kong1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
visual analog scale

研究概览

简要总结

the study is to evaluated dopplar guided angiopuncture efficacy and safety in patients with dysmenorrhea

详细描述

to conduct angiopuncture, with dopplar located perforator points and also evaluate the spectrum before and after angiopuncture therapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Primary dysmenorrhea diagnosis (≥6 months of menstrual pain scoring ≥2 on numerical rating scale) Regular menstrual cycles (28-32 days), menstrual period lasts 4 to 7 days No pelvic pathology on transvaginal ultrasound.

排除标准

  • •coagulopathy (INR >1.5) recent analgesic use (48-hour washout) secondary dysmenorrhea confirmed by laparoscopy.

研究组 & 干预措施

angiopuncture treated group

Experimental

conduct angiopuncture therapy

干预措施: conduct angiopuncture on perforator points (Other)

结局指标

主要结局

visual analog scale

时间窗: pre-treatment, immediate post-treatment, check up 1, check up 2, check up 3 (3 check ups lasts for 3 months post therapy, with each for 1 month)

to measure pain score before and after angiopuncture

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rong Han

PhD student

City University of Hong Kong

研究点 (1)

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