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PENG Block in Comparison With Anesthetic Infiltration (PAI) After Hip Hemiarthroplasty

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Trial completed Show 7 more changesShow less
    • Final enrollment: 60 participants (planned 54)
    • Primary completion date changed from estimate of Oct 31, 2025 to Aug 31, 2025
    • Eligibility criteria revised
    • Secondary endpoints: details revised at 1 of 4 entries
    • Study description revised
    • Site details revised
    • Publications: details revised at 7 of 7 entries
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Nov 2024 to Nov 1, 2024
    • Site details revised
    v2
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 goal of this intervention study is to compare the analgesic efficacy of pericapsular nerve group (PENG) block versus periarticular anesthetic infiltration (PAI) block in patients undergo hemiarthroplasty after spinal anesthesia . The main questions it aims to answer are: which block has more analgesic efficacy. which block has more motor-sparing analgesia. Researchers will compare optimal motor-sparing analgesia between PENG block and PAI after hemiarthroplasty. Participants will be divided in two groups : group receive PENG block and other group receive PAI
Trial Details
NCT Number NCT06677606
Lead Sponsor Fayoum University Hospital
Conditions
(from sponsor)		 Post Operative Pain
Related terms Postoperative Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov