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临床试验/NCT05838144
NCT05838144招募中不适用

Efficacy of Acapella on Spirometry Measures in Patients With Bronchiectasis.

South Valley University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年8月1日最近更新:
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适应症

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
1
主要终点
Spirometry measures
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

  1. Acapella group. Will use Acapella device for 3 times per day for 15 minutes for 7 days beside medications and routine chest physical therapy program .
  2. Only routine physical therapy program group ( control group). Will only take medications and routine chest physical therapy program.

详细描述

  1. Acapella group.Will use Acapella device for 3 times per day for 15 minutes for 7 days beside medications and routine chest physical therapy program.
  2. Only routine physical therapy program group( control group). Will only take medications and routine chest physical therapy program Spirometer measures such as forced vital capacity (FVC) and forced expiratory volume in the first second (FEV1) will be measured for every patient before and after the end of 7 days.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
40 Years 至 55 Years（Adult）
性别
All
接受健康志愿者
是

入选标准

  • •bronchiectasis patients.
  • •Age range between 40 to 55 years old of both gender.
  • •Cooperative patients.

排除标准

  • •Patients with severe cardiac disorders.
  • •Un controlled hypertensive patients.
  • •Un controlled diabetic patients.

结局指标

主要结局

Spirometry measures

时间窗: 7 days

FVC, FEV1

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

Shymaa yussuf abo zaid

Lecturer

South Valley University

研究点 (1)

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