Autopsy report · NCT03066401

Respiratory Variations for Assessing Blood Withdrawal 2

“insufficient inclusion rate”

The sponsor’s own words in the registry.

Life of this trial

• Registered 1 year 10 months after it had already started.
• Ran for about 1 year 5 months before it stopped.
• 5 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

University Hospital, Lille

Sponsor type

University, hospital or other

Conditions

Dysmetabolic Syndrome; Hyperferritinemia; Obese

Interventions

echography

Participants

5

Sites

1

Countries

France

Trials that died the same way

• Video-Assisted Thoracoscopic Pulmonary Vein Isolation Versus Percutaneous Catheter Ablation in Atrial Fibrillation Trial
  “Inclusion rate insufficient” (98% match in meaning)
• The Influence of Pneumoperitoneum on Minimal Invasive Cardiac Output Measurements
  “Low inclusion rate” (85% match in meaning)
• PET / CT With 18F-FDG: Does it Optimize the I 123-MIBG Imaging Results in the Search for Discriminating Factors for the Implementation of an Implantable Defibrillator?
  “Inclusion rate too slow / infeasible.” (83% match in meaning)
• Risk of Rupture of Aneurysms of the Thoracic Ascending Aorta (ATA) From the Dynamic Imaging
  “low inclusion rates” (81% 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)

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.