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Erector Spinae Plane Block Catheters and Intrathecal Morphine for Hepatic Resection

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated June 7, 2022 (before its estimated May 1, 2023 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Re-verified, no change to tracked fieldsv5
  2. Minor Study description revisedv4 See this version in full on ClinicalTrials.gov ↗
  3. Minor Start date: May 3, 2021 to May 24, 2021v3
  4. Minor Primary and study completion dates: Apr 1, 2023 to May 1, 2023 Start date: Apr 19, 2021 to May 3, 2021 · Interventions: 0.2% ropivacaine local anesthetic continuous erector spinae plane block (Drug) to 0.2% ropivacaine local anesthetic continuous erector spinae plane block (Drug), 0.2% ropivacaine local anesthetic superficially taped… · Study description expanded, about 7 wordsv2 Show 3 more changesShow less
    • Start date: Apr 19, 2021 to May 3, 2021
    • Interventions: 0.2% ropivacaine local anesthetic continuous erector spinae plane block (Drug) to 0.2% ropivacaine local anesthetic continuous erector spinae plane block (Drug), 0.2% ropivacaine local anesthetic superficially taped…
    • Study description expanded, about 7 words

    See this version in full on ClinicalTrials.gov ↗

  5. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
To determine whether the addition of erector spinae plane (ESP) catheters to existing multimodal analgesic regimen with intrathecal morphine provides superior postoperative analgesia in patients undergoing hepatic resection compared with patients not receiving ESP catheters.
Trial Details
NCT Number NCT04849455
Lead Sponsor University of California, San Diego
Conditions Hepatic Resection, Acute Pain, Anesthesia, Anesthesia, Local
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov