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Surgical Transversus Abdominis Plane Block in Pediatric Patients (TAP)

M

Mahidol University

Status

Completed

Conditions

Child

Treatments

Other: No intervention
Procedure: TAP block
Procedure: Local infiltration group

Study type

Interventional

Funder types

Other

Identifiers

NCT01548027
752/2554

Details and patient eligibility

About

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.

Full 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.

Enrollment

54 patients

Sex

All

Ages

Under 15 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age < 15 year
  2. ASA I-III
  3. Abdominal surgery : all upper abdomen and lower abdomen which would have midline incision
  4. Elective surgery

Exclusion criteria

  1. Allergic to Lidocaine or bupivacaine
  2. Delayed development
  3. Major abdominal surgery within 2 year

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 3 patient groups

No intervention
Experimental group
Description:
no injection of local anesthetic agents
Treatment:
Other: No intervention
Local infiltration group
Experimental group
Description:
patients would have 0.5 ml/kg of 0.25% bupivacaine if age \< 6 months or 1 ml/kg if age \> 6 months around the wound by surgeon. The needle will be injected in subcutaneous tissue parallel to the wound.
Treatment:
Procedure: Local infiltration group
TAP block group
Experimental group
Description:
Surgical TAP block (sTAP: Patients would have 0.5 ml/kg of 0.25% bupivacaine if age \< 6 months or 1 ml/kg if age \> 6 months
Treatment:
Procedure: TAP block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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