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Clinical Trials/NCT07280182
NCT07280182CompletedNot Applicable

Comparing the Early Postoperative Analgesic Effect of the Transmuscular Quadratus Lumborum Block Versus the Lumbar Plexus Block for Patients Undergoing Spiral Thighplasty Surgery

Menoufia University1 site in 1 country42 target enrollmentStarted: December 13, 2025Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
42
Locations
1
Primary Endpoint
Visual analogue scale score

Study Overview

Brief Summary

Whether trans muscular QLB provides postoperative analgesia compared with LPB after thigh lift surgery

Detailed Description

Adequate analgesia after spiral thigh reduction (thigh lift) is essential for early mobilization and patient satisfaction. Quadratus lumborum block (QLB) has shown analgesic efficacy comparable to lumbar plexus block (LPB) for hip area surgery with potential advantages in motor-sparing and safety

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Masking Description

Computer-generated randomization in variable blocks; allocation sealed in opaque envelopes. Blocks performed by an anesthesiologist not involved in postoperative assessment. Patients and outcome assessors are blinded. Drape and opaque dressings conceal injection sites for both groups to preserve blinding

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • ASA ( American Society of Anaesthesia) I-II
  • elective bilateral spiral thigh lift under general anesthesia
  • consent to regional block and trial participation

Exclusion Criteria

  • Coagulopathy or therapeutic anticoagulation not meeting ASRA safety windows
  • infection at injection sites
  • allergy to local anesthetics
  • preexisting significant neuropathy
  • BMI > 35 kg/m² if impeding ultrasound visualization; renal/hepatic failure; pregnancy; inability to use NRS; chronic opioid use >60 mg oral morphine equivalents/day; contraindication to study analgesics.

Arms & Interventions

Group QLB

Other

Ultrasound-Guided Trans-muscular QLB

Intervention: Ultrasound-Guided Trans-muscular QLB (Other)

Group LPB

Other

Ultrasound-Guided Posterior Lumbar Plexus (Psoas Compartment) Block

Intervention: Ultrasound-Guided Posterior Lumbar Plexus (Psoas Compartment) Block (Other)

Outcomes

Primary Outcomes

Visual analogue scale score

Time Frame: 24 hours

Visual analogue scale score at 1st,6th,12th and 24 h (where 0 is interpreted as no pain, 1-4 mild pain, 5-6 moderate pain, 7-10 severe pain)

Secondary Outcomes

  • Time for first analgesic request(24 hours)
  • Opioid consumption(24 hours)
  • Time to walk >30 (meter)(24 hours)
  • Performance Time(minutes)
  • The number of patients who develop block-related complications(24 hours)
  • the patients Satisfaction questionnaire(24 hours)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Amal Gouda Elsayed Safan

lecturer

Menoufia University

Study Sites (1)

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