Subcostal Transverse Abdominis Plane Block for Epigastric Cardiac Pacemaker Operation

  • STATUS
    Recruiting
  • End date
    Dec 31, 2023
  • participants needed
    22
  • sponsor
    Seoul National University Hospital
Updated on 15 February 2021

Summary

This prospective randomized controlled trial aims to examine the effect of subcostal transverse abdominis plane block on the postoperative pain and opioid consumption in patients (12y age) who will undergo epigastric cardiac pacemaker operation.

Patients will be allocated to either the SC TAP(subcostal transverse abdominis plane block) group or the control group (no block). Bilateral subcostal transverse abdominis plane block will be performed using 0.25% ropivacaine (0.5mL/kg for each side, MAX 20mL for each side) under ultrasound-guidance at the end of surgery.

The pain score at 10 min after PACU admin, 1, 6, 24 hours after the surgery, the total opioid consumption at 12, and 24 hours after the surgery, the total dose of additional rescue analgesia (intravenous ketololac or nalbuphine) at 12 and 24 hour after the surgery will be recorded.

Description

This prospective randomized controlled trial aims to examine the effect of subcostal transverse abdominis plane block on the postoperative pain and opioid consumption in patients (12y age) who will undergo epigastric cardiac pacemaker operation.

Patients will be allocated to either the SC TAP(subcostal transverse abdominis plane block) group or the control group (no block). Bilateral subcostal transverse abdominis plane block will be performed using 0.25% ropivacaine (0.5mL/kg for each side, MAX 20mL for each side) under ultrasound-guidance at the end of surgery.

The pain score at 10 min after PACU admin, 1, 6, 24 hours after the surgery, the total opioid consumption at 12, and 24 hours after the surgery, the total dose of additional rescue analgesia (intravenous ketololac, acetaminophen, or fentanil) at 12 and 24 hour after the surgery will be recorded.

Details
Condition Congenital Heart Disease
Treatment Control, SC TAP
Clinical Study IdentifierNCT04570878
SponsorSeoul National University Hospital
Last Modified on15 February 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients who will undergo epigastric cardiac pacemaker operation. (12 years)

Exclusion Criteria

Allergy to opioid
Allergy to local anesthetics
Coagulation disorder
Disease in the central and peripheral nervous system
Significant renal impairment (Creatinine> 3.0 mg/dl)
Significant hepatic impairment (aspartate transaminase> 120 unit/L, alanine aminotransferase> 120 unit/L)
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