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NCT04996290

Combined PENG and LFCN Block for Total Hip Arthroplasty

Completed NA Last updated 9 August 2021
What this trial tests

NA trial testing PENG + LFCN block in Anesthesia, Conduction in 40 participants. Completed in 1 October 2020.

Timeline
1 June 2020
Primary endpoint
30 September 2020
1 October 2020

Quick facts

Lead sponsorUniversity Hospital, Antwerp
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment40
Start date1 June 2020
Primary completion30 September 2020
Estimated completion1 October 2020
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Antwerp

Who can join

Adults 18 to 90, any sex, with Anesthesia, Conduction or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A clinical trial investigating the effect of a combined locoregional anesthesia technique on the postoperative analgesia outcomes after a total hip arthroplasty. A PENG block will be used in combination with a LFCN block. The results will be compared to a control group that is solely treated with intravenous analgesia. This technique aims to provide improved pain scores after surgery without interference of revalidation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of PENG + LFCN block

Trials testing the same drug.

Other University Hospital, Antwerp trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04996290.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing