quadro-iliac plane block in lumbar spine surgery

Ultrasound guided Quadro-iliac plane block for postoperative analgesia in lumbar spine surgery: a randomized controlled trial

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

PACTR

Registry ID

PACTR202601886878119

Enrollment

Registered

2026-01-05

Start date

2025-11-24

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Surgery Anaesthesia

Interventions

control group

quadroiliac plane block

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for elective lumbar spine under general anesthesia. 2. American Society of Anesthesiologists physical status (ASA) grades I, II. 3. Age 18 to 65 years old. 4. Both sex.

Exclusion criteria

Exclusion criteria: 1. Patient refusal. 2. Neuromuscular diseases. 3. Hematological diseases, bleeding or coagulation abnormality. 4. Local skin infection and sepsis at site of the block. 5. Known allergy to the study drugs. 6. Unstable cardiovascular condition. 7. Multi-traumatized patients 8. Patients on opioid analgesics or opioid abuse. 9. Obese patients (BMI >35) 10. Patient with abnormal renal functions,

Design outcomes

Primary

Measure	Time frame
cumulative fentanyl consumption during the first 24 hours after surgery.	—

Secondary

Measure	Time frame
duration of analgesia;total ketorolac consumption;visual analogue scale for pain score;number of patients required opioid;nausea and vomiting;hematoma;time to ambulate;patient satisfaction	—

Countries

Egypt

Contacts

Public ContactAmani Tarbay

lecturer A.I.T

Amany.tarbay@mans.edu.eg+201002031086

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 10, 2026