Actively Recruiting

Phase Not Applicable
Age: 40Years - 60Years
All Genders
Healthy Volunteers
NCT06476769

Combined Effects of Blow Bottle Device and Postural Drainage in Moderate to Severe Elderly COPD Patients

Led by Riphah International University · Updated on 2024-06-26

40

Participants Needed

1

Research Sites

26 weeks

Total Duration

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AI-Summary

What this Trial Is About

It will be a randomized clinical trial. Age of selected subjects will be between 40 to 70 years. Data will be collected from Wazirabad institute of cardiology. There will be 2 groups i.e. group A will receive combination of blow bottle technique and postural drainage and group B will receive postural drainage. Spirometer will be used to evaluate pulmonary functions and breathless, cough and sputum scale (BCSS) will be used to evaluate the improvement in sputum diary of patients. Interventions will be given to the patients for 20-25 minutes twice a day for 6 days per week. After data collection, data will be analyzed using SPSS version 25.

CONDITIONS

Official Title

Combined Effects of Blow Bottle Device and Postural Drainage in Moderate to Severe Elderly COPD Patients

Who Can Participate

Age: 40Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed moderate to severe GOLD (2017) COPD
  • Aged 40 to 60 years
  • Male or female
  • Hemodynamically stable patients
  • Pulmonary function test showing irreversible airflow limitation
Not Eligible

You will not qualify if you...

  • Type II diabetic mellitus
  • Systemic illness
  • Thoracic deformation or rib fracture
  • Pulmonale decompensation and signs of an unstable heart condition

AI-Screening

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Trial Site Locations

Total: 1 location

1

Wazirabad Institute of Cardiology

Multan Khurd, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

I

Iqbal Tariq, PHD

CONTACT

I

imran amjad, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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