临床试验/NCT04406012

NCT04406012已完成不适用

Analgesic Efficacy of Ultrasound Guided Paravertebral Block in Percutaneous Nephrolithotomy Patients: A Randomized Controlled Clinical Study

Eskisehir Osmangazi University0 个研究点目标入组 53 人开始时间: 2016年2月16日最近更新: 2020年9月29日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方
入组人数: 53
主要终点: Patient VAS scores

研究概览研究设计入排标准结局指标研究者记录与标识符相似试验

研究概览

简要总结

The aim of this study is to investigate the analgesic effects of thoracal paravertebral block in the patients undergoing percutaneous nephrolitotomy. Paravertebral block was applied to the study group. Conventional analgesia methods were applied to the control group.

详细描述

Randomization was divided into two groups by using closed envelope method. Postoperative pain scores at rest at 1, 2, 4, 6, 8, 10, 12, and 24 hours with VAS (0 = no pain, very severe pain = 10) using Visual Analogue Scale was made. VAS at rest and movement (coughing and taking a deep Breath) were evaluated. Patients with VAS> 4 received additional analgesics.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
主要目的: Supportive Care
盲法: Single (Investigator)

入排标准

年龄范围: 18 Years 至 65 Years（Adult, Older Adult）
性别: All
接受健康志愿者: 是

入选标准

•ASA I, II, III patients aged 18-65 who consented to undergo unilateral percutaneous nephrolithotomy were eligible for the study. 53 patients were eligible and assesed.Informed consent was signed by all patients. Patients under 18 years of age, pregnant, with known hypersensitivity to local anesthetics, bleeding diathesis, depression and / or anxiety disorder, obesity (BMI> 35kg / m2), history of pneumothorax, phrenic nerve paralysis, severe aortic stenosis were excluded. Also who did not want to participate the study.

排除标准

未提供

结局指标

主要结局

Patient VAS scores

时间窗: 24 hours

0=no pain, 10=incredible pain

次要结局

Patient Satisfaction scores(at the end of the 24 hours)

研究者

发起方

Eskisehir Osmangazi University

申办方类型

Other

责任方

Principal Investigator

主要研究者

Ferda YAMAN

Assist. Prof. Dr.

Eskisehir Osmangazi University

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