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NCT07073209 · ClinicalTrials.gov registry record · NA

PENG vs Femoral Block for Hip Fracture Analgesia

A NA study of Hip Fractures, sponsored by Weill Medical College of Cornell University.

Recruiting
Registry status
NA
Development phase
352
Enrollment target
1
Study location

NCT07073209 is a NA study of Hip Fractures that is actively recruiting participants, run by Weill Medical College of Cornell University. The registered enrollment target is 352 participants, below the 598-participant average among 15 other Hip Fractures trials with a reported enrollment target (41% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07073209, a NA study of Hip Fractures, is actively recruiting participants, sponsored by Weill Medical College of Cornell University.

RECRUITING
Registry status
NA
Development phase
352 participants
Enrollment target
1
Study location

Study Summary

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.

Conditions Studied

Interventions

  • PROCEDURE PENG Block Administration
  • PROCEDURE Femoral Block Administration
  • DRUG Bupivacaine , epinephrine Dexamethasone

Study Locations (1)

New York

  • Weill Cornell Medicine - Manhattan

Trial Details

FieldValue
Enrollment Target 352 participants
Start Date 2025-07-10
Est. Completion 2027-04
Phase NA

What the Registry Record Tells You About NCT07073209

The ClinicalTrials.gov registry entry for NCT07073209 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 352 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 598-participant average among 15 other Hip Fractures trials with a reported enrollment target (41% lower). The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hip Fractures appearing as the primary indexed condition, and to 3 interventions - of which PENG Block Administration is the first listed.

NCT07073209 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT07073209 about?

NCT07073209 is a clinical study titled "PENG vs Femoral Block for Hip Fracture Analgesia". 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 ...

What is the current status of trial NCT07073209?

This trial is currently recruiting. It is a NA study. The enrollment target is 352 participants. The study started on 2025-07-10. Estimated completion is 2027-04.

What conditions does trial NCT07073209 study?

This clinical trial studies the following conditions: Hip Fractures.

What interventions are being tested in trial NCT07073209?

The interventions under investigation include: PENG Block Administration (PROCEDURE), Femoral Block Administration (PROCEDURE), Bupivacaine , epinephrine Dexamethasone (DRUG).

Who is sponsoring clinical trial NCT07073209?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07073209 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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