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Erector Spinae Plane Block Versus Quadratus Lumborum Block For Postoperative Analgesia After Abdominal Hysterectomy

Erector Spinae Plane Block Versus Quadratus Lumborum Block For Postoperative Analgesia After Abdominal Hysterectomy; A Randomized Comparative Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05541588
Enrollment
64
Registered
2022-09-15
Start date
2022-07-07
Completion date
2023-02-10
Last updated
2024-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

Brief summary

The aim of this study is to compare the analgesic efficacy of erector spinae plane block and quadratus lumborum block after abdominal hysterectomy surgery and postoperative opioid consumption.

Interventions

PROCEDUREperipheral nerve block

ultrasound guided nerve block

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with American Society of Anesthesiologists (ASA) physical status 1-3. * scheduled for abdominal hysterectomy surgery.

Exclusion criteria

* History of allergy to the medications used in the study. * Contraindication to regional anesthesia as coagulopathy, local infection. * Severe hepatic impairment (child C). * Sever Renal dysfunction (creatinine clearance \< 30). * Psychiatric or mental disorder affecting patient ability to interpret VAS score. * Body mass index (BMI) ≥ 40 or ≤ 18 kg/m2. * ASA IV. * Patient refusal.

Design outcomes

Primary

MeasureTime frameDescription
Post-operative pain24 hoursPost-operative pain severity assessed by visual analog scale (VAS) (range from 0-10., 0 no pain, 10 worst pain ).

Secondary

MeasureTime frameDescription
Cumulative post-operative opioid consumption24 hoursopioid consumption
The onset of 1st analgesic request24 hourstime needed for 1st request of rescue analgesia

Other

MeasureTime frameDescription
Incidence of complications24 hourspostoperative nausea and vomiting(PONV), hematoma, local anaesthetic toxicity (LAT)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026