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Influence of Analgesic Technique on Post Operative Rehabilitation After Median Laparotomy

Study acronym: QORRECTCATH
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Primary completion date: Oct 10, 2025 to Oct 10, 2028
    • Study completion date: Apr 10, 2026 to Apr 10, 2029
    v9
  2. Minor Study sites: 1 to 2
    • Secondary endpoints: 12 to 15
    v8
  3. Minor Study description expanded, about 131 wordsv7
  4. Notable Primary completion date: Oct 10, 2023 to Oct 10, 2025
    • Study completion date: Apr 10, 2024 to Apr 10, 2026
    • Site contact updated
    v6
  5. Minor Re-verified, no change to tracked fieldsv5
Show 3 earlier versionsHide 3 earlier versions
  1. Notable Primary endpoint revised
    • Eligibility criteria expanded, about 50 words
    • Secondary endpoints: details revised at 12 of 12 entries
    v4
  2. Minor Re-verified, no change to tracked fieldsv3
  3. Notable Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Sep 1, 2023 to Oct 10, 2023
    • Study completion date: Mar 1, 2024 to Apr 10, 2024
    • Start date changed from estimate of Sep 1, 2021 to Oct 11, 2021
  1. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Randomized controlled trial (1:1) in two parallel groups, multicentric, open-label, comparing two locoregional anesthesia (LRA) techniques as integral parts of multimodal analgesia: the control group will benefit from epidural anesthesia, while the experimental group will benefit from bilateral placement of catheters in the sheath of the rectus abdominis muscles.
Trial Details
NCT Number NCT04985695
Lead Sponsor Centre Hospitalier Régional Metz-Thionville
Conditions
(from sponsor)
Laparotomy
Enrollment 110 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov