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Postoperative Pain Management for Hip Surgeries: UltrasoundGuided Suprainguinal Fascia Iliaca Compartment Block Versus Suprainguinal Fascia Iliaca Compartment Block in Combination With Sciatic Nerve Block

Postoperative Pain Management for Hip Surgeries: UltrasoundGuided Suprainguinal Fascia Iliaca Compartment Block Versus Suprainguinal Fascia Iliaca Compartment Block in Combination With Sciatic Nerve Block

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07787442
Enrollment
30
Registered
2026-08-26
Start date
2025-11-02
Completion date
2026-06-02
Last updated
2026-08-26

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

Conditions

Postoperative Pain

Brief summary

The aim of the Study is to compare the analgesic efficacy and clinical outcomes of suprainguinal fascia iliaca block (SIFIB) alone versus SIFIB combined with sciatic nerve block (SNB) in patients undergoing hip surgery.

Detailed description

The aim of the Study is to compare the analgesic efficacy and clinical outcomes of suprainguinal fascia iliaca block (SIFIB) alone versus SIFIB combined with sciatic nerve block (SNB) in patients undergoing hip surgery. 1. Primary Objectives: Time for first rescue analgesia. 2. Secondary Objectives: * Numerical Rating Scale (NRS) scores at rest and during movement at 6 hours, 12 hours, 24 hours, and 48 hours after surgery. * Total opioid consumption within the first 24 hours post-surgery. * Postoperative incidence and severity of motor blockade in the affected limb associated with each block technique (measured using the Modified Bromage Scale). * Technical difficulty and duration of administering each block.

Interventions

DRUGBupivacaine injection

Bupivacaine injection

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age: 18 - 70 years old. * Sex: Both sexes. * American Society of Anesthesiologists (ASA) physical status I , II, III, IV. * Hip surgeries e.g.: Total hip arthroplasty, Hemi-arthroplasty, Fracture neck of femur under spinal anesthesia

Exclusion criteria

* Refusal to participate. * Known allergy to local anesthetics. * Coagulopathy or anticoagulant therapy contraindicating regional anesthesia. * Pre-existing neurological deficits in the lower limbs. * Infection at the injection site. * Severe cognitive impairment or inability to assess pain (e.g., advanced dementia). * Failed spinal anesthesia. * Body mass index (BMI) \>40 kg / m²

Design outcomes

Primary

MeasureTime frameDescription
Time for first rescue analgesiaNumerical Pain Score in PACU, 6 hrs, 12 hrs, 24 hrs and 48 hrs postoperativeTime to first request for rescue analgesia: Defined as the time interval from the end of procedure until the patient's first complaint of pain with a Numerical Rating Scale (NRS) score ≥ 4 and requests pain relief

Secondary

MeasureTime frameDescription
Motor Block AssessmentThe Modified Bromage Scale at 2 , 6 , 12 and 24 hours postoperativelyMotor Block Assessment: Assessed using the Modified Bromage Scale (0 = no block; 1 = unable to raise extended leg; 2 = unable to flex knee; 3 = unable to move foot or knee) at 2, 6, 12, and 24 hours postoperatively

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 27, 2026