Actively Recruiting

Phase Not Applicable
Age: 30Years - 50Years
All Genders
NCT06454305

Effects of ACBT and Blow Bottle Technique in Patients With Abdominal Surgeries Under General Anesthesia

Led by Riphah International University · Updated on 2024-06-12

44

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A postoperative pulmonary complication (PPC) is the most common serious complication after Abdominal surgery under GA which lead to longer hospital stays and have deleterious outcomes on lung volumes, mucociliary clearance, accumulation of mucus, saliva and cough reflex. Chest physiotherapy for airway clearance which includes postural drainage, chest percussion, vibrations, Along with these, breathing exercises such ACBT and Blow bottle technique are recommended to clear secretion which aid in enhancing pulmonary function by effectively mobilizing and eliminating excess bronchial secretions. This study of randomized clinical trial will check the comparative effect of ACBT and Blow Bottle Technique in patients with abdominal surgeries under GA by taking a sample of 44 patients through non probability convenience sampling technique. Subject of both gender will be included between the age of 30 to 50 years who will undergoes with elective abdominal surgeries under GA (Cholecystectomy, Hysterectomy ,Appendectomy, Hemorrhoidectomy) and Laparoscopic /open. Elective surgeries under spinal anesthesia, emergency surgeries, cardiothoracic surgeries and hemodynamically unstable subjects will be excluded. 22 subjects will receive ACBT and other 22 subjects will receive Blow bottle technique for 20 minutes duration per session, two sessions per day for a period of 5 days. The status of airway clearance, oxygen saturation and lungs volumes will be measured pre and post intervention on day 1 and at the end of 5th day by using BCSS, Pulse oximeter and Spirometer.

CONDITIONS

Official Title

Effects of ACBT and Blow Bottle Technique in Patients With Abdominal Surgeries Under General Anesthesia

Who Can Participate

Age: 30Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 30 to 50 years
  • Male or female gender
  • Undergoing elective abdominal surgeries under general anesthesia including cholecystectomy, hysterectomy, appendectomy, hemorrhoidectomy
  • Both laparoscopic and open surgeries
  • Postoperative pulmonary complications such as sputum retention, hypoxemia, or impaired pulmonary function starting immediately after surgery
Not Eligible

You will not qualify if you...

  • Elective surgeries under spinal anesthesia
  • Emergency surgeries
  • Cardiothoracic surgeries
  • Neurological impairment
  • Prolonged surgeries
  • Psychological impairment
  • Head and neck surgeries
  • Vascular surgeries
  • Hemodynamically unstable patients

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cairns Railway Hospital Lahore

Lahore, 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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