Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07272577

Erector Spinae Plane Block on Postoperative Analgesia in Patients Undergoing Laparoscopic Abdominal Surgeries

Efficacy of Erector Spinae Plane Block on Postoperative Analgesia in Patients Undergoing Laparoscopic Abdominal Surgeries

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Assiut University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study aims to evaluate the efficacy of the erector spinae plane block (ESPB) on postoperative analgesia in patients undergoing laparoscopic abdominal surgeries.

Detailed description

Laparoscopic surgery is associated with less pain, fewer wound infections, reduced hospital stay, reduced morbidity and mortality, and early return to work and improved overall quality of life. The role of ESPB as a better analgesic modality in reducing 24-hour opioid consumption has recently been established for post-operative analgesia in breast surgeries, video-assisted thoracoscopic surgery, and cardiothoracic surgeries.

Conditions

Interventions

TypeNameDescription
OTHERErector spinae plane blockPatients will receive an ultrasound-guided erector spinae plane block.

Timeline

Start date
2025-12-10
Primary completion
2026-04-01
Completion
2026-04-01
First posted
2025-12-09
Last updated
2025-12-11

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07272577. Inclusion in this directory is not an endorsement.