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Efficacy of Variable Volume Truncal Blocks in Upper Limb Orthopedic Surgery

StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated March 5, 2025 (before its estimated December 1, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Primary completion date: May 1, 2025 to Dec 1, 2025
    • Study completion date: Jun 1, 2025 to Dec 1, 2025
    • Site details revised
    • Eligibility criteria expanded, about 1 word
  2. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
aim of this study is to compare the effect of selective truncal blocks, performed at different doses and volumes, on the onset times of motor and sensory blocks required for anesthesia in patients scheduled for hand, wrist, forearm, and elbow surgeries. Completing the operation under regional anesthesia will be considered a successful block.
Trial Details
NCT Number NCT06664203
Lead Sponsor Gaziosmanpasa Research and Education Hospital
Conditions
(from sponsor)		 Pain Management, Anaesthesia Complication
Related terms Agnosia, Postoperative Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov