Autopsy report · NCT05273918
Monitoring and Evaluation of a Cognitive Behavioral Therapy Program Focused on Attention and Emotion Regulation for Children With Fetal Alcohol Spectrum Disorder
Cause of deathStaffing, sites or logistics
“logistic problem and absence of coordinating Investigator”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Na
- Sponsor
- Centre Hospitalier Universitaire de la Réunion
- Sponsor type
- University, hospital or other
- Conditions
- Fetal Alcohol Spectrum Disorders; Hyperactivity Disorder; Attention Deficit
- Interventions
- cognitivo-comportmental therapy; body mediation
- Participants
- 0
- Sites
- 3
- Countries
- France, Reunion
Trials that died the same way
- Performance of Diuretic Stress Test in Predicting Short Term Renal Recovery in Oliguric Critically-ill Patients Recovery in the Short Term
“departure of the coordinating investigator from another institution” - Hypnosis to Reduce Pain and Drugs for Shoulder Dislocation Management
“departure of the study coordinating investigator” - Intravenous Isosorbide Dinitrate Versus Sublingual Isosorbide Dinitrate for the Relief of Acute Anginal Episodes in Acute Coronary Syndrome (ACS) Patients
“LOGISTIC DIFFICULTIES” - Insulin Pre-treatment for Steroid-associated Hyperglycemia in Pregnant Diabetic Patients
“Time constraints of primary investigator.” - PNE Plus Exercise Versus Exercise for Chronic Rotator Cuff Tendinopathy
“Logistic issues”
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.