Autopsy report · NCT03551717

Retinal Microvascularization and Cardiovascular Disease

“Lack of inclusion”

The sponsor’s own words in the registry.

Life of this trial

• Registered 2 months after it had already started.
• Ran for about 1 year 1 month before it stopped.
• 155 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

Centre Hospitalier Universitaire Dijon

Sponsor type

University, hospital or other

Conditions

High Cardiovascular Risk Patients; Low Cardiovascular Risk Patients

Interventions

Optical Coherence Tomography angiography; Fundus; cardiac ultrasound scan

Participants

155

Sites

1

Countries

France

Trials that died the same way

• Development of a Predictive Score for Local Complications of Femoral Bifurcation Surgery
  “lack of inclusions” (97% match in meaning)
• Pronostic Value of Endothelial Dysfunction in Heart Failure
  “Not enough inclusions” (85% match in meaning)
• Transfusion Effects in Myelodysplastic Patients: Limiting Exposure
  “Too few inclusions” (82% match in meaning)
• Bedside Therapeutic Monitoring of β-Lactam Levels in Newborns, Children and Adolescents Admitted to Intensive Care.
  “insufficient inclusions” (81% match in meaning)
• Effects of Early Musical Intervention on Prevalence and Severity of Paroxysmal Sympathetic Hyperactivity After Severe Traumatic Brain Injury
  “inclusion difficulties” (81% match in meaning)

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.