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Clinical Trials in Ireland / NCT07046052
Recruiting

PENG Block: Continuous Infusion vs. Programmed Intermittent Bolus in Neck of Femur Fracture

NCT07046052 · tracked via the Priya Life Science Ireland tracker
Sponsor
University College Cork
Phase
N/A
Started
2024-03-28
Last updated
2025-07-01

Condition(s) studied

Hip FractureAnalgesia Post Fracture

Investigational drug(s) / intervention(s)

continuous infusion of levobupivacaineProgrammed Intermittent Bolus of Levobupivacaine

continuous infusion of levobupivacaine: Participants in this arm will receive a continuous infusion of levobupivacaine via a regional anaesthesia catheter placed in the PENG fascial space. The total dose over 24 hours will be equivalent in both arms of the study.

Programmed Intermittent Bolus of Levobupivacaine: Participants in this arm will receive a timed pre-set bolus dose of levobupivacaine via a regional anaesthesia catheter placed in the PENG fascial space. The total dose over 24 hours will be equivalent in both groups.

Study summary

Pericapsular Nerve Group Block (PENG) is an effective regional anaesthesia modality in providing analgesia following neck of femur fracture. Continuous PENG techniques, using indwelling catheters and infusions of local anaesthetic, facilitate the continuation of analgesia for a number of days following hip fracture surgery. It is unclear from the published literature whether an optimal strategy of local anaesthetic delivery has been characterized.

Similar doses of local anaesthetic agents can be administered by either continuous infusion or timed intermittent bolus. It is unclear whether one dosing strategy is superior to the other in the context of hip fracture analgesia. The study aims to evaluate the clinical efficacy of both dosing strategies in patients undergoing hip fracture surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * English-speaking * over the age of 18 years * hemiarthroplasty for fractured neck of femur * able to provide written consent. Exclusion Criteria: * under 50kg body weight. * unable to provide consent due to incapacity * pregnant women * vulnerable adults under state guardianship * Patients with pre-existing chronic pain disorders or with a history of long-term opioid use * those with contraindications to a peripheral nerve block such as local site infection, allergy to local anaesthetic or those who are coagulopathic

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cork University Hospital Cork Cork Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07046052 on ClinicalTrials.gov ↗ ← All trials in Ireland