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The Basel BOMP-AID Randomized Trial

Study acronym: BOMP-AID
StatusRecruiting
PhasePhase 4
Started
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Record History

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  1. Notable Primary completion date: Dec 2026 to Dec 2027v13
  2. Notable Primary completion date: Dec 2024 to Dec 2026
    • Study completion date: Dec 2025 to Dec 2027
    v12
  3. Minor Re-verified, no change to tracked fieldsv11
  4. Notable Trial status: Not Yet Recruiting to Recruitingv10 Show 4 more changesShow less
    • Primary completion date: Oct 2023 to Dec 2024
    • Study completion date: Oct 2024 to Dec 2025
    • Start date changed from estimate of Nov 2021 to Jan 3, 2022
    • Site details revised
  5. Notable Primary completion date: Oct 2022 to Oct 2023
    • Start date: Nov 2020 to Nov 2021
    • Study completion date: Oct 2023 to Oct 2024
    v9
Show 7 earlier versionsHide 7 earlier versions
  1. Notable Primary completion date: Mar 2022 to Oct 2022
    • Start date: Jul 2020 to Nov 2020
    • Study completion date: Mar 2023 to Oct 2023
    v8
  2. Notable Start date: Apr 2020 to Jul 2020v7
  3. Notable Start date: Dec 1, 2019 to Apr 2020v6 Show 5 more changesShow less
    • Primary completion date: Nov 30, 2021 to Mar 2022
    • Study completion date: Feb 28, 2022 to Mar 2023
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: 4 to 6
    • Study description expanded, about 49 words
  4. Notable Primary completion date: Mar 31, 2021 to Nov 30, 2021v5 Show 5 more changesShow less
    • Start date: Sep 1, 2019 to Dec 1, 2019
    • Enrollment target: 258 to 190
    • Study completion date: Mar 31, 2022 to Feb 28, 2022
    • Eligibility criteria expanded, about 37 words
    • Study description expanded, about 361 words
  5. Notable Start date: Apr 1, 2019 to Sep 1, 2019v4
  6. Notable Start date: Dec 1, 2018 to Apr 1, 2019
    • Primary completion date: Nov 30, 2020 to Mar 31, 2021
    • Study completion date: Dec 31, 2020 to Mar 31, 2022
    v3
  7. Notable Start date: Jul 1, 2018 to Dec 1, 2018
    • Primary completion date: Sep 30, 2020 to Nov 30, 2020
    v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Delirium is a neurobehavioural syndrome that frequently develops in the postoperative and/or ICU setting. The incidence of elderly patients who develop delirium during hospital stay ranges from 11-82%. Delirium was first described more than half a century ago in the cardiac surgery population, where it was already discovered as a state that might be accompanied by serious complications such as prolonged ICU and hospital stay, reduced quality of life and increased mortality. Furthermore, the duration of delirium is associated with worse long-term cognitive function in the general ICU population. This long-term experience with delirium suggests a high socioeconomic liability and has been a focus of many studies. The aforementioned consequences of delirium are observed in all of three subtypes: hypoactive, hyperactive, and mixed. Pharmacological treatment options for hypoactive delirium are lacking. Since patients in hypoactive delirium suffer from disturbed circadian rhythm, the investigators suggest that the administration of melatonin as a promising possibility in these patients to shorten delirium duration and to lower its severity. Previous investigations confirmed loss of melatonin rhythm in patients that had developed delirium thus reasoning the study hypothesis. In this randomized study, the investigators aim to test the hypothesis that the reinstitution of a normal circadian rhythm by the administration of melatonin compared to placebo after diagnosis of hypoactive delirium, decreases the duration of delirium and reduces the transmission to a form of agitated delirium. The administration might have to be repeated several times to achieve resolution of delirium.
Trial Details
NCT Number NCT03438526
Lead Sponsor University Hospital, Basel, Switzerland
Conditions
(from sponsor)
Hypoactive Delirium
Enrollment 190 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov