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Comparison of Cryoablation of Pericapsular Nerve Group (PENG) to Fascia Iliaca Catheter in Patients With a Hip Fracture

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 12 months later Oct 1, 2026 → Oct 1, 2027
See other at-risk trials from University of Minnesota

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary completion pushed from Oct 1, 2026 to Oct 1, 2027
    • Eligibility criteria expanded, about 5 words
  2. Re-verified, no change to tracked fieldsv6
  3. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    v5
  4. Start date: Aug 1, 2024 to Oct 1, 2024
    • Primary completion date: Aug 1, 2026 to Oct 1, 2026
    • Study completion date: Feb 1, 2027 to Oct 1, 2027
    v4
  5. Start date: Jun 1, 2024 to Aug 1, 2024
    • Primary completion date: Jun 1, 2026 to Aug 1, 2026
    • Study completion date: Dec 1, 2026 to Feb 1, 2027
    v3
  6. Start date: Mar 1, 2024 to Jun 1, 2024
    • Primary completion date: Mar 1, 2026 to Jun 1, 2026
    • Study completion date: Sep 1, 2026 to Dec 1, 2026
    v2
  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to determine if patients with hip fractures who undergo cryoablation of the PENG have improved pain control 30 days from surgery when compared to those who have a fascia iliaca catheter.
Trial Details
NCT Number NCT06278987
Lead Sponsor University of Minnesota
Conditions
(from sponsor)		 Hip Fractures
Related terms Hip Fractures
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov