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Comparison of Spinal Anesthesia Adjuvant and Quadratus Lumborum Block on the Opioid Requirement and Perioperative Pain of Laparoscopic Kidney Transplant Donor

U

University of Indonesia (UI)

Status

Enrolling

Conditions

Laparoscopic Donor Nephrectomy
Perioperative Pain Management

Treatments

Procedure: General Anesthesia
Procedure: Spinal anesthesia adjuvant
Procedure: Quadratus Lumborum Block (QLB)

Study type

Interventional

Funder types

Other

Identifiers

NCT06764667
IndonesiaUAnes048

Details and patient eligibility

About

This study aims to compare the effectiveness of spinal anesthesia adjuvant and quadratus lumborum block on the opioid requirement and perioperative pain on patients undergoing laparoscopic kidney transplant donor.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18-65 years undergoing laparoscopic donor nephrectomy
  • Patients with BMI ≤ 35 kg/m2
  • Patients with American Society of Anesthesiology (ASA) physical status 1-2
  • Patients who are willing to participate in this study

Exclusion criteria

  • Cardiovascular disease (uncontrolled stage 2 hypertension, heart failure, arrhytmia)
  • Recent onset cerebrovascular diseasae of < 3 months
  • Infection on spinal site
  • Coagulopathy
  • Elevated intracranial pressure
  • Severe renal or liver dysfunction
  • Valvular heart disease or atrioventricular block

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Quadratus lumborum block
Active Comparator group
Description:
Patients in this arm will receive quadratus lumborum block with 20-30 ml of 0.25% Bupivacaine after induction of anesthesia and after operation.
Treatment:
Procedure: Quadratus Lumborum Block (QLB)
Procedure: General Anesthesia
Spinal anesthesia adjuvant
Experimental group
Description:
Patients in this arm will receive 10 mg 0.5% hyperbaric Bupivacaine, 100 mcg Morphine, 100 mcg Sulfas Atropine, and 0.9% normal saline to total volume of 4 ml before induction of anesthesia.
Treatment:
Procedure: Spinal anesthesia adjuvant
Procedure: General Anesthesia

Trial contacts and locations

1

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Central trial contact

Dita Aditianingsih, Prof.

Data sourced from clinicaltrials.gov

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