临床试验/PACTR202201626031418

PACTR202201626031418招募中未知

Comparison between paracervical block anesthesia and Spinal anesthesia regarding endometrial sampling in women with abnormal uterine bleeding

faculity of medicine Suez canal university0 个研究点目标入组 240 人开始时间: 2021年11月12日最近更新: 2023年5月29日

适应症

试验速览

阶段: 未知
状态: 招募中
发起方
入组人数: 240

研究概览入排标准研究者记录与标识符相似试验

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

•1-Age from 25-60 years with abnormal uterine bleeding
•2- Patients with ultrasound findings of endometrial or cervical pathology which will require cervical and endometrial sampling.
•3-Patients who were ASAI (American Society of Anesthesiologists') physical status Grade I, ASA II (ASA Grade II).
•4-Controlled clinical illness as DM and hypertension.
•5-No history of allergic reaction to the anaesthetic agents.

排除标准

•1-Patients with mental or behavioral disorders that will impair or interfere with perioperative and follow-up procedures,
•2-Bleeding tendency,
•3- patients with cervicitis or pelvic inflammatory disease before treatment.
•4-A known sensitivity to used drugs,
•5-Pregnancy,
•6-vaginismus

研究者

发起方

faculity of medicine Suez canal university

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