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Clinical Trials/NCT01548027
NCT01548027
Completed
Not Applicable

Efficacy of Surgical Transversus Abdominis Plane Block for Postoperative Pain Relief Following Abdominal Surgery in Pediatric Patients.

Mahidol University1 site in 1 country54 target enrollmentJuly 2012
ConditionsChild

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Child
Sponsor
Mahidol University
Enrollment
54
Locations
1
Primary Endpoint
opioids consumption
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The objective of this study to determine the effect of surgical transversus abdominis plane block and local infiltration for postoperative pain control in major abdominal surgery compare with control group.

Detailed Description

Most children experience postoperative pain after major abdominal surgery. They may have ineffective ventilation, following atelectasis and pneumonia if receive inadequate pain management. There are several methods used for pain relief such as epidural block, intravenous analgesia with local infiltration, transversus abdominis plane (TAP) block by ultrasound guided and surgical TAP block. Therefore, the investigators would like to compare the effectiveness of postoperative pain control with TAP block. However, TAP block in children need experience and ultrasound. The investigators decided to do surgical TAP block performing by inject from peritoneum point to skin instead.

Registry
clinicaltrials.gov
Start Date
July 2012
End Date
July 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age \< 15 year
  • Abdominal surgery : all upper abdomen and lower abdomen which would have midline incision
  • Elective surgery

Exclusion Criteria

  • Allergic to Lidocaine or bupivacaine
  • Delayed development
  • Major abdominal surgery within 2 year

Outcomes

Primary Outcomes

opioids consumption

Time Frame: 24 hours

total opioids consumption in first 24 hours postoperatively

Secondary Outcomes

  • Time to first analgesic(24 hr)

Study Sites (1)

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