Autopsy report · NCT02724631
TubeClear® Evaluation in Pediatric Patients (Phase I)
Cause of deathSlow enrollment
“Unable to recruit; study determined not feasible to continue”
Life of this trial
- Registered 8 months before it started.
- Ran for about 3 years 8 months before it stopped.
- 1 participant enrolled.
- Results were posted on the registry 4 years 8 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Children's Hospital of Philadelphia
- Sponsor type
- University, hospital or other
- Conditions
- Enteral Nutrition
- Interventions
- TubeClear® intervention
- Participants
- 1
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Effects of Statin Therapy on Vascular Properties and Outcomes in Diastolic Heart Failure Patients
“Unable to recruit into the study” - A Study to Determine Serum and Skin Biopsy Biomarkers in Patients Receiving Topical Corticosteroid (TCS) and Following TCS Withdrawal
“Unable to meet the study's recruitment goals” - Therapy With Zoledronic Acid in Patients With Multiple Myeloma Stage I
“Recruitment in study could not be reached after 8 yrs of recruiting” - Evaluation of the Versamed iVent in the Transport of Patients Receiving Mechanical Ventilation
“Unable to recruit adequately” - Infantile Colic: Study of the Efficacy of Lactobacillus GG (ATCC 53103) Plus Chamomile in Breastfeeding Infants
“Unable to recruit study participants”
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.