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Pain relief in hip fracture patients using latest ultrasound technology.

Comparison of analgesic efficacy between Fascia iliaca compartment block (FICB), Femoral nerve block (FNB) and PEricapsular Nerve Group block (PENG) in patients with Hip Fractures: A randomized double blind trial. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040557
Enrollment
175
Registered
2022-02-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: M848- Other disorders of continuity of bone

Interventions

Intervention1: ultrasound- guided supra-inguinal fascia iliaca block: Group I: S-FICB- ultrasound- guided supra-inguinal fascia iliaca block with 40ml of 0.25% Ropivacaine + 4mg (1ml) dexamethasone on

Sponsors

Dr Rajendra Kumar Sahoo
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 40 years and above of American Society of Anesthesiologists physical status (ASA) I-III with hip fracture scheduled for surgery under spinal anesthesia.

Exclusion criteria

Exclusion criteria: 1.Patient refusal to participate 2.Contraindication to Spinal anesthesia or peripheral nerve blocks 3.Patients with significant cognitive impairment 4.Patients on opioids for chronic pain

Design outcomes

Primary

MeasureTime frame
-Visual analogue score (VAS) at rest and on passive 15° limb lifting, 30 min after the block. - Ease of spinal positioning (EOSP). Timepoint: -Visual analogue score (VAS) at rest and on passive 15° limb lifting, 30 min after the block and it will be noted once and then patient will be taken inside operation theatre for spinal anesthesia. - Ease of spinal positioning (EOSP) score while positioning for spinal anesthesia will be noted once.

Secondary

MeasureTime frame
-Visual analogue score (VAS) at rest and on passive 15° limb lifting at 3, 6, 12 and 24 hours postoperatively. -Time to first rescue analgesic (tramadol) request. -Total opioid consumption (in mg) in first 24 hours. -Patient´s satisfaction. -Quadriceps strength at 6, 12 and 24 hours. Timepoint: up to 24 hours in the post operative period.

Countries

India

Contacts

Public ContactDr Rajendra kumar Sahoo

Kalinga Institute Of Medical Sciences

rajendra.sahoo@kims.ac.in7750008259

Outcome results

None listed

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