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Study identifier: NCT07073209 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

PENG vs Femoral Block for Hip Fracture Analgesia

Condition: Hip Fractures  ·  Sponsor: Weill Medical College of Cornell University

PhaseNA
Planned participants352
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to compare the Pericapsular Nerve Group (PENG) block with femoral block for hip fracture pain. Participants presenting to the hospital with a diagnosis of hip fracture and consenting to analgesic block will receive either a PENG or femoral block. The choice of block will be dictated by a randomized monthly schedule, and all participants presenting during each four-week period will receive the designated block. A sub-group analysis will be performed to determine any difference in efficacy in participants with intracapsular versus extracapsular fractures.

This description comes directly from the study's public registry record.

Talk to the study team

Michele Steinkamp, BSN, RN  ·  212-746-2953  ·  mls9004@med.cornell.edu

Mark Abdelmassih, B.S.  ·  212-746-2774  ·  maa4068@med.cornell.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Weill Cornell MedicineManhattan, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07073209