Autopsy report · NCT03735940
Clinical Evaluation Program of DeltaScan (ICU)
Cause of deathStaffing, sites or logistics
“The pandemic caused a rising tide phenomenon on our primary outcomes 1) Delirium detection (increased by visit reduction \& masked staff) and 2) Admission duration (increased by reorganizations \& quarantines 'impact on being discharged)”
Life of this trial
- Registered 4 months before it started.
- Ran for about 2 years 4 months before it stopped.
- 3,630 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- UMC Utrecht
- Sponsor type
- University, hospital or other
- Conditions
- Delirium
- Interventions
- Spot monitoring device, excl. Sham
- Participants
- 3,630
- Sites
- 1
- Countries
- Netherlands
Trials that died the same way
- Bardoxolone Methyl in Patients With Connective Tissue Disease-associated Pulmonary Arterial Hypertension - CATALYST
“Exposure of these high-risk patients to clinic or in-person visits during the pandemic presented an unacceptable risk to their health” - Early Kangaroo Mother Care in Gambian Hospitalised Unstable Neonates
“In response to COVID pandemic” - Study of the Safety and Efficacy of Nabiximols Oromucosal Spray Versus Placebo in Patients With Post-traumatic Stress Disorder
“The decision to suspend this study was based upon evaluation of pandemic-related challenges impacting both clinical trial sites and potential participants. This suspension was initiated prior to site activation and participant recruitment.” - Laser Treatment for Vulvar Lichen Sclerosus
“Recruitment was significantly impacted by the COVID-19 pandemic.” - Yogurt Supplementation to Alter Bone Biomarkers, the Gut Microbiota and Inflammation in Older Adults
“Due to the onset of the COVID-19 pandemic”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.