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Perioperative Lidocaine and Ketamine in Abdominal Surgery

StatusActive, Not Recruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated May 21, 2025 (before its estimated December 2025 completion). Its status may not reflect the trial's current state.

Record History

  1. Primary and study completion dates: Dec 2024 to Dec 2025v9
  2. Primary and study completion dates: Dec 2023 to Dec 2024
    • Trial status: Recruiting to Active, Not Recruiting
    • Site details revised
    v8
  3. Primary and study completion dates: Dec 2022 to Dec 2023v7
  4. Primary completion date: Dec 2021 to Dec 2022
    • Study completion date: Jun 2022 to Dec 2022
    v6
  5. Primary completion date: Jun 2021 to Dec 2021v5
Show 3 earlier versionsHide 3 earlier versions
  1. Re-verified, no change to tracked fieldsv4
  2. Site contact updatedv3
  3. Start date changed from estimate of Oct 2019 to Oct 15, 2019v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 investigators propose to test the hypothesis that perioperative infusions of lidocaine and/or ketamine reduce opioid consumption and pain scores in adults recovering from elective inpatient abdominal surgery.
Trial Details
NCT Number NCT04084548
Lead Sponsor The Cleveland Clinic
Conditions
(from sponsor)		 Postoperative Pain
Related terms Postoperative Pain
Enrollment 420 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov