UnknownNot Applicable

Posterior Quadratus Lumborum Block Using 0.125% Versus 0.25% Bupivacaine for Analgesia in Children Undergoing LPEC

Thailand50 participantsStarted 2021-08-15

Plain-language summary

The aim of the present study is to evaluate and compare the analgesic efficiency of the difference concentration between 0.125% and 0.25% bupivacaine provided by ultrasound guided posterior quadratus lumborum block undergoing LPEC in children

Who can participate

Age range1 Year – 6 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Children scheduled for laparoscopic percutaneous extraperitoneal closure(LPEC) for pediatric inguinal hernia and hydrocele * ASA I-II physical status patients * Complete inform consent for intervention Exclusion Criteria: * Contraindication for regional anesthesia * Sensitive to local anesthetic agent, opioid or acetaminophen * Previous history of abdominal surgery * History of neuromuscular disease * G6PD deficiency

What they're measuring

Quality of postoperative analgesia

Timeframe: 24 hours after surgery

Trial details

NCT IDNCT04998071

SponsorQueen Sirikit National Institute of Child Health

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2022-05-31

Contact for this trial

SUWITCHA TAMRONGCHOTE, MD

+66989425629 S.NI.KTAMP@GMAIL.COM

View on ClinicalTrials.gov More Postoperative Pain trials