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A study to compare post operative analgesic efficacy of SIFI block and QL block.

Post operative analgesic efficacy of suprainguinal fascia block (SIFI) and quadratus lumborum block in total hip replacement: A prospective randomized controlled trial. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/086035
Enrollment
96
Registered
2025-04-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: M161- Unilateral primary osteoarthritisof hip

Interventions

Intervention1: GROUP S Supra Inguinal Fascia Iliaca Block Group (SIFIB): Patients will receive a suprainguinal fascia iliaca block using ultrasound guidance with local anaesthetic 0.2% ropivacaine 40

Sponsors

Dr Rama Raman Ravi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1-3 Patient under go Total Hip Replacement surgery of isolated hip pathology

Exclusion criteria

Exclusion criteria: Participants with pre-existing chronic pain/opioid dependency, unmanaged coagulopathy/anticoagulation, cognitive impairment hindering pain assessment, BMI more then 35, anticipated technical challenges for the block, contraindications to regional anesthesia, or polytrauma will be excluded.

Design outcomes

Primary

MeasureTime frame
1.To compare the postoperative pain intensity at rest at 6 hours of suprainguinal fascia iliaca (SIFI) block and quadratus lumborum (QL) block in patients undergoing total hip replacement (THR), using Visual Analog Scale [VAS] as the post operative pain score.Timepoint: 6 hours—

Secondary

MeasureTime frame
1. To compare the postoperative pain intensity on movement at 6 hours and at rest and on movement at 2, 12, 24 hours of suprainguinal fascia iliaca (SIFI) block and quadratus lumborum (QL) block in patients undergoing total hip replacement (THR), using pain scores Visual Analog Scale [VAS] as the post op pain score.Timepoint: 24 hours;2. To evaluate the total opioid requirement in the first 24 hours post-surgery for each group.Timepoint: 24 hours;3. To assess time to first analgesic request for each block (rescue analgesia).Timepoint: ;4. To assess the time for first-time independent ambulation after surgery in each block mobility score (0-2) and Evaluate time to achieve score of 2 post surgery.Timepoint: ;5. To assess Patient satisfaction using Likert s scale (1-5).Timepoint: 48 hours;6. To document and compare the incidence of block-related complications, including motor weakness, hematoma, infection, etc.Timepoint: 48 hours—

Countries

India

Contacts

Public ContactDr Rama Raman ravi

All India Institute of Medical Sciences Gorakhpur

santoshtata76@gmail.com7800130773

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026