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Intrathecal Morphine for Analgesia in Video-assisted and Robotic-assisted Thoracic Surgery

StatusRecruiting
PhasePhase 4
Started
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Record History

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  1. Primary completion date: Jun 1, 2026 to Jun 1, 2027
    • Study completion date: Sep 1, 2026 to Sep 1, 2027
    v10
  2. Eligibility criteria expanded, about 2 wordsv9
  3. Lead sponsor: University of Chicago to Northwestern Universityv8 Show 4 more changesShow less
    • Primary completion date: Jan 1, 2026 to Jun 1, 2026
    • Study completion date: Mar 1, 2026 to Sep 1, 2026
    • Eligibility criteria expanded, about 3 words
    • Study title expanded, about 2 words
  4. 2 versions Re-verified since Oct 11, 2024, no change to tracked fieldsv6-v7
  5. Primary completion date: Sep 1, 2024 to Jan 1, 2026
    • Study completion date: Dec 1, 2024 to Mar 1, 2026
    v5
Show 3 earlier versionsHide 3 earlier versions
  1. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jul 1, 2023 to Sep 29, 2023
    • Site details revised
    v4
  2. Start date: Jan 1, 2023 to Jul 1, 2023v3
  3. Start date: Sep 1, 2022 to Jan 1, 2023v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
VATS/RATS is widely used for diagnosis and treatment of intrathoracic conditions. Despite many benefits, postoperative pain continues to be intense after VATS/RATS. The optimal strategy for pain management has not been defined. In this randomized, placebo-controlled, double-blinded clinical investigation, investigators hypothesize that 5 mcg/kg intrathecal morphine will decrease postoperative analgesic consumption and reduce pain.
Trial Details
NCT Number NCT05351229
Lead Sponsor Northwestern University
Conditions
(from sponsor)		 Pain, Postoperative
Related terms Postoperative Pain
Enrollment 90 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov