Comparative Effects of Acapella and Positive End Expiratory Pressure Device among Patients with Laparoscopic Surgery

Phase 4

Recruiting

• Conditions: Condition 1: Cholecystectomy. Condition 2: Splenectomy.; Acquired absence of other specified parts of digestive tract; Hyposplenism; Z90.4; D73.0

• Registration Number: IRCT20191117045462N9
• Lead Sponsor: Riphah International University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 44

Inclusion Criteria

Age criteria of 35-55yrs
Patients undergone Laparoscopic Surgery (Cholecystectomy, Liver Biopsy, Ectopic Pregnancy, Splenectomy, and Ovarioectomy)
Both male and female

Exclusion Criteria

Patients body mass index < 15 kg.m-2 or > 30 kg.m-2
Patient’s history of respiratory tract infection within three months
Patient’s baseline arterial partial pressure of oxygen (PaO2) < 70 mmHg or arterial partial pressure of carbon dioxide (PaCO2) > 50 mmHg; baseline forced expiratory volume in 1 s (FEV1) < 30% of predicted.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Dyspnea. Timepoint: Pre post treatment. Method of measurement: will be checked by Multidimensional Dyspnea Profile (MDP).;Sputum Diary. Timepoint: pre post treatment. Method of measurement: Breathlessness, Cough, Sputum Scale (BCSS).;Pulmonary Function Test. Timepoint: pre post treatment. Method of measurement: portable spirometer.