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Decreasing Preoperative Stress to Prevent Postoperative Delirium and Postoperative Cognitive Decline in Cardiac Surgical Patients.

Study acronym: DESTRESS-SURG
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date: Aug 2025 to Aug 2028
    • Study completion date: Nov 2025 to Nov 2028
    v6
  2. Trial status: Not Yet Recruiting to Recruitingv5 Show 4 more changesShow less
    • Primary completion date: May 2024 to Aug 2025
    • Start date changed from estimate of Jan 2023 to Jul 27, 2023
    • Study sites: 0 to 1
    • Study completion date: Aug 2024 to Nov 2025
  3. Start date: Oct 2022 to Jan 2023
    • Secondary endpoints: 38 to 41
    v4
  4. Start date: May 2022 to Oct 2022
    • Secondary endpoints: 35 to 38
    v3
  5. Primary completion date: Sep 2023 to May 2024
    • Start date: Sep 2021 to May 2022
    • Study completion date: Dec 2023 to Aug 2024
    v2
  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Patients undergoing cardiac surgery often complain of anxiety before a major operation and the resulting stress. This circumstance is a risk factor for mental problems that may occur after the operation (e.g., delirium or memory deficits). This study aims to prevent these discomforts by a preoperative relaxation intervention.
Trial Details
NCT Number NCT05036538
Lead Sponsor Heart and Brain Research Group, Germany
Conditions
(from sponsor)		 Preoperative Stress, Postoperative Cognitive Dysfunction, Postoperative Delirium
Related terms Emergence Delirium, Postoperative Cognitive Complications
Enrollment 125 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov