Autopsy report · NCT03343158
Orphans and Vulnerable Children Risk Screening Tool Research Study (Zimbabwe)
Cause of deathStaffing, sites or logistics
“Significantly more resources would have been necessary to complete the study.”
Life of this trial
- Ran for about 5 months before it stopped.
- 2,260 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Elizabeth Glaser Pediatric AIDS Foundation
- Sponsor type
- University, hospital or other
- Conditions
- Orphans, Children, Adolescents; Vulnerable Children, Adolescents; Community-based
- Participants
- 2,260
- Sites
- 1
- Countries
- Zimbabwe
Trials that died the same way
- Philadelphia Immediate Transport in Penetrating Trauma Trial
“The study was not feasible due to logistical elements” - HBOT Late Radiation Tissue Injury
“Lack of resources to complete the study” - Noninvasive NAVA Versus NIPPV in Low Birthweight Premature Infants
“Insufficient resources available to complete the study” - Mindfulness in Medical Training
“Not enough resources to proceed with the study” - Capecitabine and Temozolomide for Treatment of Recurrent Pituitary Adenomas
“the study had a low accrual rate”
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.