Autopsy report · NCT05173116
Evaluation of the API-VIGIE Monitoring System: Program to Reduce Emergency Visits for Severe Paroxysmal Alcoholism
Cause of deathStaffing, sites or logistics
“protocol not implemented for logistical reasons in the recruiting center, possible rescheduling.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Sponsor
- Centre Hospitalier Arras
- Sponsor type
- University, hospital or other
- Conditions
- Intoxication;Alcohol;Acute; Emergencies
- Interventions
- Medical Outcomes Study Short Form 36 (SF 36); observationnal study
- Participants
- 0
- Sites
- 1
- Countries
- France
Trials that died the same way
- Dietary Guidelines for Americans-Ultra Processed Study
“Change in administrative priorities. Protocol has been published, but recruitment never started.” - Early Administration of the Lutein/Zeaxanthin in Premature Newborns
“Recruitment was not possible” - Clinical Management of Neuropathic Pain With Ramelteon
“Recruitment did not accrue as expected.” - Anti PD-L1 Antibody + Anti CTLA-4 Antibody in Combination With Hormone Therapy in Patients With Hormone Receptor Positive HER2-negative Recurrent or Metastatic Breast Cancer
“Recruiting was not possible” - World Health Organization Disability Assessment Schedule II (WHODAS-II) for Patients With Symptomatic Lumbar Spinal Stenosis
“Recruitment was so slow, that it made the study impossible. Organizational changes made it impossible for recruiting centers to continue recruitment”
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.