Ultrasound Guided Transversus Abdominis Plane Block in Pediatric Surgery

• Status: Completed
• Trial end date: 2017-10-01
• Target enrollment: 0
• Participant gender: Male

Summary

The primary objective of this study is to assess differences in postoperative pain experienced by pediatric patients having transversus abdominis plane block block with bupivacaine (0.125% and 0.25%) compared with control group will receive conventional iv analgesia after Laparoscopic surgery.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Abdelrady S Ibrahim, MD
• Treatments: Bupivacaine

Criteria

Inclusion Criteria:

• ASA I-II physical status patients.

• Genders Eligible for Study :male.

• All children scheduled for laparoscopic surgery between the ages of 1and 5 years.

• Duration of Laparoscopic procedure not exceeding 90 minutes.

• Written informed consent from parent of guardian .

Exclusion Criteria:

• Sensitivities to local anesthetics.

• Significant renal, liver, or cardiac disease.

• Surgery requiring an open procedure