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Comparison of Fascia Iliaca Block (FIB) versus Pericapsular Nerve Group (PENG) Block combined with Lateral Femoral Cutaneous Nerve (LFCN) versus PENG Block combined with FIB for postoperative pain control in Proximal Femoral Nail Antirotation (PFNA) Surgery

Comparison of Fascia Iliaca Block (FIB) versus Pericapsular Nerve Group (PENG) Block combined with Lateral Femoral Cutaneous Nerve (LFCN) versus PENG Block combined with FIB for postoperative pain control in Proximal Femoral Nail Antirotation (PFNA) Surgery

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240529011
Enrollment
66
Registered
2024-05-29
Start date
2024-05-10
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

Hip fracture patients undergoing proximal femoral nail antirotation (PFNA) surgery under spinal anesthesia in Ramathibodi hospital PFNA, hip fracture

Interventions

1. PENG block is first performed following the original description by Giron-Arango et al . The US probe is placed in a transverse plane over the anterior inferior iliac spine (AIIS), and subsequently
PF (combined PENG block and FIB),PL (combined PENG and LFCN block),F (FIB alone)

Sponsors

Faculty of medicine, Ramathibodi hospital, Mahidol university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Hip fractures undergo PFNA for primary fixation under SA., 2. American Society of Anesthesiologists (ASA) physical status I-IV, 3. Body weight > 40 kg

Exclusion criteria

Exclusion criteria: 1. Body mass index (BMI) < 18 or > 35 kg/m2, 2. Contraindications to perform SA and PNB (e.g., patient refusal, skin puncture site infection, bleeding tendency, coagulopathy), 3. Hypersensitivity to local anesthetics, 4. Comorbidity such as neurocognitive impairment, communication problems, hepatic or renal failure, neuromuscular disease of lower extremities, 5. Chronic pain with history of long-term opioid use or abuse

Design outcomes

Primary

MeasureTime frame
Static and dynamic pain score 24 hours postoperatively Numeric rating scale score

Secondary

MeasureTime frame
Spinal block positioning 30 minutes post-procedure Ease of spinal positioning (EOSP) score,Pain score during SA positioning 30 minutes post-procedure NRS,Opioid consumtion 24 hours postoperatively MME (morphine milligram equivalent),Static and dynamic pain score 0, 6, 12, 48 hours postoperatively Numeric rating scale score,Time to first rescue opioid request Post-procedure Period of time,Quadriceps strength 24 hours postoperatively Bromage score

Countries

Thailand

Contacts

Public ContactTanat Chuepongpan

Faculty of Medicine Ramathibodi Hospital, Mahidol University

tanat.chue@gmail.com0896295518

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026