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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05838144
Other study ID # PT-IMG-02/2023-505
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2023
Est. completion date October 20, 2023

Study information

Verified date July 2023
Source South Valley University
Contact Shymaa Y Abo zaid
Phone 01010941685
Email shaymaayoussef397@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date October 20, 2023
Est. primary completion date September 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 55 Years
Eligibility Inclusion Criteria: 1. bronchiectasis patients. 2. Age range between 40 to 55 years old of both gender. 3. Cooperative patients. Exclusion Criteria: 1. Patients with severe cardiac disorders. 2. Un controlled hypertensive patients. 3. Un controlled diabetic patients.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Acapella device
Group A. Will use Acapella device.
Other:
Only routine chest physical therapy program
Group B. Will take medications and perform routine chest physical therapy program.

Locations

Country Name City State
Egypt Shymaa yussuf abo zaid Cairo

Sponsors (1)

Lead Sponsor Collaborator
South Valley University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Spirometry measures FVC, FEV1 7 days
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