Autopsy report · NCT03136900
Impact on the Nitrogen Balance, Autonomy, Safety and Tolerance of Enteral Diets Made of With Nutrilon Without Lactose® Fortified by Concentration Versus by Maltodextrin and Oil Supplementation,After Surgery for Congenital Heart Disease, in Infants.
Cause of deathSlow enrollment
“Recuitment to slow”
Life of this trial
- Ran for about 2 years 11 months before it stopped.
- 41 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Queen Fabiola Children's University Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Congenital Heart Disease in Children
- Interventions
- Nutrilon without lactose® fortified by concentration; Nutrilon without lactose® fortified by Maltodextrin and oil supplementation
- Participants
- 41
- Sites
- 1
- Countries
- Belgium
Trials that died the same way
- Temodar (Temozolomide), Bevacizumab, Lithium and Radiation for High Grade Glioma
“Due to slow accrual”
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.