Comparing breathing techniques for patients after abdominal surgery
Comparative Effects of Active Cycle of Breathing Technique and Blow Bottle Technique to Prevent Post-operative Pulmonary Complications in Patients With Abdominal Surgeries Under General Anesthesia
This study is testing two different breathing techniques to see which one helps people recover better after having abdominal surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 44 (estimated) |
| Ages | 30 Years to 50 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab Province) |
| Trial ID | NCT06454305 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effects of two breathing techniques, the Active Cycle of Breathing Technique (ACBT) and the Blow Bottle Technique, on patients who have undergone elective abdominal surgeries under general anesthesia. The study aims to determine which technique is more effective in reducing postoperative pulmonary complications, such as sputum retention and hypoxemia. A total of 44 patients aged 30 to 50 will be randomly assigned to receive one of the two interventions to assess their impact on pulmonary function and recovery. The trial will utilize a non-probability convenience sampling method for participant selection.
Who should consider this trial
Good fit: Ideal candidates are adults aged 30 to 50 who are scheduled for elective abdominal surgeries under general anesthesia.
Not a fit: Patients undergoing emergency surgeries, spinal anesthesia, or those with certain medical conditions such as neurological impairments will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve recovery outcomes and reduce complications for patients undergoing abdominal surgeries.
How similar studies have performed: Previous studies have shown positive outcomes with similar breathing techniques in improving pulmonary function post-surgery, suggesting potential for success in this trial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 30 to 50 Gender: male/Female Both Elective surgeries Under General Anesthesia (Cholecystectomy, Hysterectomy ,Appendectomy, Hemorrhoidectomy) Laparoscopic /open both POCs: Sputum retention, hypoxemia, impair pulmonary function From the day 0 or immediate after surgery Exclusion Criteria: * Elective surgeries under spinal anesthesia Emergency surgeries Cardiothoracic surgeries Neurological impairment, prolong surgeries Psychological impairment Head and neck surgeries and vascular surgeries Hemodynamically unstable
Where this trial is running
Lahore, Punjab Province
- Cairns Railway Hospital Lahore — Lahore, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Sidra Afzal, PP-DPT — Riphah International University
- Study coordinator: Iqbal Tariq, Phd
- Email: iqbal.tariq@riphah.edu.pk
- Phone: 03338236752
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.