Efficacy of Pericapsular Nerve Group Block
Study Comparing the Efficacy of Pericapsular Nerve Group (PENG) Block and Facia Iliaca Compartment Block (FICB) in Hip Fracture - A Prospective Randomised Controlled Trial
1 other identifier
interventional
100
1 country
1
Brief Summary
Hip fracture is a common orthpaedic problem especially in elderly population. Fascia iliaca compartment block (FICB) and femoral nerve block are well-established technique as part of peri-operative multimodal analgesia for hip fractures. Reviews have shown peripheral nerve blocks including FICB, femoral nerve block and 3-in-1 block could reduce both pain and opioid consumption compared with systematic analgesia. However, there are also literature suggesting that some nerves that account for the major hip joint sensory innervation are not consistently covered. As a result, a new ultrasound guided regional technique, Pericapsular Nerve Group Block (PENG) was introduced in 2018. The primary aim of this study is to compare the analgesic effect of PENG block and FICB in terms of pain score during post-operative period. It also compares the range of movement, quadriceps power and other parameters related to physical functions of the operated hip as secondary outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2021
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 15, 2021
CompletedFirst Submitted
Initial submission to the registry
November 29, 2021
CompletedFirst Posted
Study publicly available on registry
December 13, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedDecember 1, 2023
November 1, 2023
2.1 years
November 29, 2021
November 29, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Pain score at rest on postoperative day 1
Measure pain score at rest using numerical rating scale from 0 to 10, where 0 is no pain and 10 is the worst pain
on postoperative day 1
Study Arms (2)
Pericapsular Nerve Group Block
EXPERIMENTAL30ml 0.3% Ropivacaine will be injected between psoas muscle and iliopubic eminence.
Fascia iliaca compartment block
ACTIVE COMPARATOR30ml 0.3% Ropivacaine will be injected into fascia iliaca compartment.
Interventions
Nerve block targeting major hip joint sensory nerves.
Routine nerve block for hip fracture surgery.
Eligibility Criteria
You may qualify if:
- ASA I-II
- Age 18 or above
- Scheduled for hip fracture corrective surgery in Queen Mary Hospital
- Chinese patients
- Able to provide informed oral and written consent
- Abbreviated Mental Test (AMT) 7 or above
You may not qualify if:
- Patient refusal
- ASA III or above
- Allergy to local anaesthetics, opioids, paracetamol, NSAID including COX-2 inhibitors
- Operation delayed for more than 2 days on admission
- Pre-existing peripheral neuropathy or history of stroke
- Preoperative non-walker
- Pre-existing osteoarthritis of knee (KL grade 4)
- Multiple fractures (additional to hip fracture)
- Sepsis
- Impaired renal function (Defined as preoperative creatinine level \>120 μmol or eGFR \<50% of normal reference for their age group
- Patient with coagulopathy (Platelet \< 100 or INR \>1.5)
- Prior surgery at the inguinal or supra-inguinal area
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Timmy Chan
Hong Kong, Hong Kong
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Timmy CW Chan, MBBS
The University of Hong Kong
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
November 29, 2021
First Posted
December 13, 2021
Study Start
November 15, 2021
Primary Completion
December 31, 2023
Study Completion
December 31, 2024
Last Updated
December 1, 2023
Record last verified: 2023-11