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ENROLLING BY INVITATION
NCT07023991
PHASE1

Dexmedetomidine Added to Bupivacaine for ESP Block in Children Undergoing Lower Abdominal Surgeries

Sponsor: Ain Shams University

View on ClinicalTrials.gov

Summary

This study aims to evaluate the effect of adding dexmedetomidine to bupivacaine in erector spinae plane (ESP) blocks on the duration of postoperative analgesia in pediatric patients undergoing lower abdominal surgery. Effective postoperative pain control in children remains a clinical challenge, and regional anesthesia techniques such as the ESP block have shown promise in improving outcomes. In this randomized, double-blind clinical trial, pediatric patients scheduled for elective lower abdominal surgeries will be assigned to receive either bupivacaine alone or bupivacaine combined with dexmedetomidine as part of an ultrasound-guided ESP block. The primary outcome is the duration of postoperative analgesia, defined as the time from the block until the first request for rescue analgesia. Secondary outcomes include total analgesic consumption and postoperative pain scores

Official title: Effect of Adding Dexmedetomidine to Bupivacaine in US- Guided Erector Spinae Plane Block for Post-operative Pain Management in Pediatric Patients Undergoing Lower Abdominal Surgeries

Key Details

Gender

All

Age Range

1 Year - 7 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2025-05-01

Completion Date

2025-08-31

Last Updated

2025-06-17

Healthy Volunteers

Yes

Interventions

DRUG

Bupivacaine

Bupivacaine will be used in an ESP block to provide postoperative analgesia.

DRUG

Dexmedetomidine

Dexmedetomidine will be added to bupivacaine in the ESP block to evaluate its effect on duration of postoperative analgesia.

Locations (1)

Ain Shams University

Cairo, Egypt, Egypt