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Analgesic Effect of Supraclavicular Block and Interscalene Analgesia Versus an Intercostobrachial Nerve Block Versus PCA in Forearm Surgery

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Primary and study completion dates: Nov 30, 2024 to Dec 30, 2025v8
  2. Primary and study completion dates: Apr 30, 2024 to Nov 30, 2024v7
  3. Primary and study completion dates: Dec 30, 2023 to Apr 30, 2024v6
  4. Start date: Nov 10, 2022 to Dec 10, 2022
    • Primary and study completion dates: Oct 30, 2023 to Dec 30, 2023
    v5
  5. Primary and study completion dates: Apr 30, 2023 to Oct 30, 2023v4
Show 2 earlier versionsHide 2 earlier versions
  1. Primary and study completion dates: Jan 30, 2023 to Apr 30, 2023v3
  2. Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v2
  1. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 etiology of tourniquet pain is complex, and the study team hypothesizes that blocking with Interscalene brachial plexus block (ISBPB) is more efficient in decreasing the incidence of tourniquet pain in comparison with other techniques. As there is a paucity of studies that evaluate the effect of intercostobrachial nerve (ICBN) block and ISBPB and Patient-Controlled Analgesia (PCA) with a supraclavicular brachial plexus block (SCBPB) on tourniquet pain in forearm surgery, Therefore, we established this randomized study to compare ISBPB and ICBN and PCA with fentanyl with SCBPB in terms of the incidence and severity of tourniquet pain in patients undergoing forearm surgery.
Trial Details
NCT Number NCT05602636
Lead Sponsor Al-Azhar University
Conditions
(from sponsor)		 Forearm Surgery, US-Guided Supraclavicular Block, Interscalene Analgesia, Tourniquet Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov