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Recruiting NCT06291389

NCT06291389 Intraoperative Peak Airway Pressure Changes on Postoperative Pulmonary Function After Muscle Plication

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Clinical Trial Summary
NCT ID NCT06291389
Status Recruiting
Phase
Sponsor Al-Azhar University
Condition Abdominal Compartment Syndrome
Study Type OBSERVATIONAL
Enrollment 120 participants
Start Date 2024-03-10
Primary Completion 2026-12-15

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age 50 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 120 participants in total. It began in 2024-03-10 with a primary completion date of 2026-12-15.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

An abdominal panniculus excision procedure is known as an abdominoplasty (panniculectomy). Musculofascial plication is a crucial aspect of abdominoplasty, especially for patients with significant divarication of the recti muscles. This study aimed to evaluate the effect of intraoperative changes in peak airway pressure (PAP) after muscle plication on postoperative pulmonary function.

Eligibility Criteria

Inclusion Criteria: * age ranged between 20 and 50 years old, * American Society of Anesthesiologists (ASA) physical status classification I * came for abdominoplasty operation Exclusion Criteria: * anemia or hemoglobin levels below 11g/dl * bleeding problems * cardiovascular disorders * restrictive and obstructive respiratory disease * abdominoplasty without plication.

Contact & Investigator

Central Contact

Neveen Kohaf, Ph.D

✉ nevenabdo@azhar.edu.eg

📞 +201060383012

Principal Investigator

Neveen Kohaf, ph.d

PRINCIPAL INVESTIGATOR

Al-Azhar University

Frequently Asked Questions

Who can join the NCT06291389 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, up to 50 Years, studying Abdominal Compartment Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06291389 currently recruiting?

Yes, NCT06291389 is actively recruiting participants. Contact the research team at nevenabdo@azhar.edu.eg for enrollment information.

Where is the NCT06291389 trial being conducted?

This trial is being conducted at Tanta, Egypt.

Who is sponsoring the NCT06291389 clinical trial?

NCT06291389 is sponsored by Al-Azhar University. The principal investigator is Neveen Kohaf, ph.d at Al-Azhar University. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology