Compare the Effect of Incentive Spirometry Versus Chest Mobilization on Oxygenation and Chest Exp… (NCT07109934) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Compare the Effect of Incentive Spirometry Versus Chest Mobilization on Oxygenation and Chest Expansion for Patient Undergoing Upper Abdominal Surgery: A Randomized Clinical Trial
Iraq112 participantsStarted 2025-01-22
Plain-language summary
This study compares the effects of incentive spirometry and chest mobilization on oxygenation and chest expansion in patients after upper abdominal surgery. It is a randomized clinical trial that aims to determine which intervention more effectively improves respiratory function. The findings likely reveal that both methods positively impact lung expansion and oxygenation, but one may be superior in enhancing recovery and preventing postoperative pulmonary complications.
Who can participate
Age range
20 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Adult aged 18\> 60 years
. posted for upper abdominal surgery.
. Accepted to participate in the study
Exclusion criteria
. . Patients exhibiting unstable hemodynamic parameters characterized by arterial pressure below 100 mmHg systolic and below 60 mmHg diastolic, and mean arterial pressure (MAP) below 80 mmHg.
. Uncooperative patients or individuals with limited comprehension or inability to proficiently operate the gadget .
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Tape measuring
Timeframe: 6 time point at which the measurement is assessed for both study and control groups divided in to tow days, 3 times per day as following after 1 hours , after 8 hours and after 16 hours
2
Physiological Evaluation:
Timeframe: 6 time point at which the measurement is assessed for both study and control groups divided in to tow days, 3 times per day as following after 1 hours , after 8 hours and after 16 hours