NCT05154318

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2021

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 15, 2021

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

November 29, 2021

Completed
14 days until next milestone

First Posted

Study publicly available on registry

December 13, 2021

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

December 1, 2023

Status Verified

November 1, 2023

Enrollment Period

2.1 years

First QC Date

November 29, 2021

Last Update Submit

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

EXPERIMENTAL

30ml 0.3% Ropivacaine will be injected between psoas muscle and iliopubic eminence.

Procedure: Pericapsular Nerve Group Block

Fascia iliaca compartment block

ACTIVE COMPARATOR

30ml 0.3% Ropivacaine will be injected into fascia iliaca compartment.

Procedure: Fascia iliaca compartment block

Interventions

Nerve block targeting major hip joint sensory nerves.

Pericapsular Nerve Group Block

Routine nerve block for hip fracture surgery.

Fascia iliaca compartment block

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Acute Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Timmy CW Chan, MBBS

    The University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Timmy CW Chan, MBBS

CONTACT

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

Locations