Actively Recruiting
Effects of Intraoperative Peak Airway Pressure Changes on Postoperative Pulmonary Function After Muscle Plication in Abdominoplasty Operations
Led by Al-Azhar University · Updated on 2026-01-06
120
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
A
Al-Azhar University
Lead Sponsor
B
Benha University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research investigates how changes in peak airway pressure (PAP) during muscle tightening in abdominoplasty surgery affect lung function after the operation. The focus is on patients undergoing abdominal panniculus excision, especially those with significant separation of the abdominal muscles. The study is observational and aims to better understand the impact of these intraoperative changes on postoperative breathing. The procedure studied involves abdominoplasty, also called panniculectomy, where excess skin and fat are removed from the abdomen and the abdominal wall muscles are tightened by musculofascial plication. The study observes changes in peak airway pressure during the surgery to see how they relate to lung function afterwards. No additional treatments or interventions are given as this is an observational study. Participants are monitored for peak airway pressure during surgery and for lung function after surgery using measures such as tidal volume and respiratory rate within 24 hours. Oxygen therapy duration and length of hospital stay are also recorded up to one week following surgery. The study lasts through the immediate postoperative period, with assessments focused on breathing and recovery after the muscle tightening part of abdominoplasty.
CONDITIONS
Brief Title
Intraoperative Peak Airway Pressure Changes on Postoperative Pulmonary Function After Muscle Plication
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 20 and 50 years old
- American Society of Anesthesiologists (ASA) physical status classification I
- Scheduled for abdominoplasty operation with muscle plication
You will not qualify if you...
- Anemia or hemoglobin levels below 11g/dl
- Bleeding problems
- Cardiovascular disorders
- Restrictive and obstructive respiratory disease
- Abdominoplasty without muscle plication
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 24 hours postoperatively
Participants undergo abdominoplasty with muscle plication and are monitored for intraoperative peak airway pressure changes and immediate postoperative pulmonary function.
1 surgical visit and 1 postoperative visit within 24 hours
Duration - Up to 1 week after surgery
Participants are observed during recovery including oxygen therapy and hospital stay.
Daily visits or assessments during hospital stay for up to 1 week
Trial Site Locations
Total: 1 location
1
Neveen Kohaf
Tanta, Egypt, Egypt, 11865
Actively Recruiting
Research Team
N
Neveen Kohaf, Ph.D
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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