Effects of Pericapsular Nerve Group Block Applied in Patients Undergoing Hip Fracture Surgery.

StatusCompleted
PhaseNot applicable
Started

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Record History

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  1. Minor Trial completed
    • Eligibility criteria expanded, about 7 words
    • Site details revised at 2 of 2 sites
  2. Notable Primary completion date: Jun 30, 2025 to Dec 30, 2025
    • Study completion date: Jul 30, 2025 to Jan 30, 2026
    v9
  3. Minor Primary completion date: Mar 28, 2025 to Jun 30, 2025
    • Study completion date: May 30, 2025 to Jul 30, 2025
    v8
  4. Minor Primary completion date: Dec 28, 2024 to Mar 28, 2025
    • Study completion date: Dec 31, 2024 to May 30, 2025
    v7
  5. Minor Primary completion date: Nov 8, 2024 to Dec 28, 2024
    • Study completion date: Nov 30, 2024 to Dec 31, 2024
    v6
Show 4 earlier versionsHide 4 earlier versions
  1. Minor Primary completion date: Aug 8, 2024 to Nov 8, 2024
    • Study completion date: Sep 30, 2024 to Nov 30, 2024
    v5
  2. Minor Primary completion date: Jun 8, 2024 to Aug 8, 2024
    • Study completion date: Jul 31, 2024 to Sep 30, 2024
    v4
  3. Minor Primary completion date: May 8, 2024 to Jun 8, 2024v3
  4. Minor Primary completion date: Mar 21, 2024 to May 8, 2024
    • Study completion date: Apr 2024 to Jul 31, 2024
    v2
  1. Minor Study First Submitted
  • 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.
In this study, it was aimed to compare the multimodal analgesia application or the pericapsular nerve group (PENG) block methods in patients undergoing hip surgery. The effectiveness and benefit rate of the PENG block in postoperative pain will be evaluated. Postoperative pain, need for additional analgesia, range of motion of the hip joint, mobilization time, length of hospital time and adverse events in patients undergoing hip fracture surgery with and without PENG block will be investigated.
Trial Details
NCT Number NCT06183541
Lead Sponsor Umraniye Education and Research Hospital
Conditions
(from sponsor)
Hip Fractures, Pain, Postoperative
Related terms Hip Fractures, Postoperative Pain
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov