Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
100 participants
INTERVENTIONAL
2021-11-15
2024-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Fascia iliaca compartment block (FICB) and femoral nerve block are well-established technique as part of peri-operative multimodal analgesia for hip fractures. Cochrane review has shown peripheral nerve blocks including FICB, Femoral nerve block and 3-in-1 block could reduce both pain at 30 minute and opioid consumption compared with systemic analgesia. In particular, FICB is found to be superior to opioids for pain control on movement, preoperative analgesic consumption, time to first analgesic request, and time to perform spinal anaesthesia. However, literature suggests that the obturator nerve is not consistently covered.
The anterior hip capsule which contributes the major hip joint sensory innervation is supplied by femoral nerve (FN), obturator nerve (ON) and accessory obturator nerve (AON). As a result, a novel ultrasound guided regional technique, Pericapsular Nerve Group Block (PENG) was introduced in 2018, targeting the above 3 nerves. This is very important as the obturator nerve is also blocked with this technique. Case reports showed reduction in pain scores compared with baseline 30 minutes after block placement and no clinically evident quadriceps weakness was detected.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Pericapsular Nerve Group Block
30ml 0.3% Ropivacaine will be injected between psoas muscle and iliopubic eminence.
Pericapsular Nerve Group Block
Nerve block targeting major hip joint sensory nerves.
Fascia iliaca compartment block
30ml 0.3% Ropivacaine will be injected into fascia iliaca compartment.
Fascia iliaca compartment block
Routine nerve block for hip fracture surgery.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pericapsular Nerve Group Block
Nerve block targeting major hip joint sensory nerves.
Fascia iliaca compartment block
Routine nerve block for hip fracture surgery.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
Exclusion Criteria
* 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
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
The University of Hong Kong
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr. Chan Chi-Wing
Dr
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Timmy CW Chan, MBBS
Role: PRINCIPAL_INVESTIGATOR
The University of Hong Kong
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Timmy Chan
Hong Kong, , Hong Kong
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Timmy Chan, MBBS
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
UW21-382
Identifier Type: -
Identifier Source: org_study_id