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Effects of Analgesia Nociception Index (ANI)-Guided Analgesia on Postoperative Bowel Function.

StatusUnknown
PhaseNot applicable
Started
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Record status
This record was last updated September 5, 2024 (before its estimated October 14, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Changed Registry marked status Unknown (sponsor has not verified the record since Sep 2024); last known: Recruiting
  2. Eligibility criteria shortened, about 3 wordsv6
  3. Primary and study completion dates: Oct 14, 2023 to Oct 14, 2025v5
  4. Primary completion date: Oct 14, 2022 to Oct 14, 2023v4
  5. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Nov 30, 2021 to Nov 29, 2021
    • Study title shortened, about 5 words
    v3
  6. Start date: Nov 9, 2021 to Nov 30, 2021
    • Secondary endpoints revised (12)
    • Study title shortened, about 4 words
    v2
  7. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Investigators will examaine the effects of Analgesia Nociception Index (ANI)-guided analgesia on postoperative bowel function recovery in laparoscopic colorectal surgery. This is a prospective randomized-controlled study. Investigators will randomly divide the patients into two groups. In ANI group, remifentanil infusion rate during anesthesia will be adjusted according to ANI monitoring. In Control group, remifentanil infusion rate during anesthesia will be adjusted according to the conventional method of blood pressure and heart rate monitroing. And Investigators will evalualte the bowel function recovery in both groups after surgery, and compare between the two groups.
Trial Details
NCT Number NCT05122078
Lead Sponsor Gangnam Severance Hospital
Conditions
(from sponsor)		 Postoperative Bowel Function Recovery
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov