Autopsy report · NCT00161694
Use of Sucrose to Relieve Pain During Eye Exams in Infants
Cause of deathFutility
“results did not show intervention was beneficial”
Life of this trial
- Registered 2 months after it had already started.
- 300 participants planned (an estimate, not an actual count).
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Weill Medical College of Cornell University
- Sponsor type
- University, hospital or other
- Conditions
- Apnea of Prematurity; Retinopathy of Prematurity; Pain
- Interventions
- sucrose solution
- Participants
- 300 (planned, not actual)
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Development and Dissemination of Oral Health Risk Assessment and Referral Guidelines
“Published study provided evidence that intervention would provide little effect; study not approved by provider community.” - A Safety and Efficacy Study to Determine if Giving Intravenous Fish Oil Helps Children With Liver Disease
“study intervention was approved by the FDA” - BIIB023 Proof-of-Concept Study in Participants With Lupus Nephritis
“Results from pre-specified criteria did not demonstrate sufficient efficacy to warrant continuation of the study.” - Penicillin Allergy Risk-Stratification and Delabeling of Low-Risk Patients
“screening challenges that prevented the intervention from being implemented” - Study to Evaluate the Clinical Benefit Response in Cancer Patients With Advanced Disease With AMT2003 Versus Placebo
“Lack of efficacy. Stopped at first interim evaluation point”
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.