Autopsy report · NCT02535845
Developing a Self-persuasion Intervention Promoting Adolescent HPV Vaccination: Feasibility Trial
Cause of deathSlow enrollment, also staffing, sites or logistics
“Halted early due to poor accrual and lack of time to receive intervention procedures adjacent to a clinic visit post randomization.”
Life of this trial
- Registered 2 years 4 months before it started.
- Ran for about 1 year 1 month before it stopped.
- 22 participants enrolled.
- Results were posted on the registry 5 years after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- University of Texas Southwestern Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Human Papillomavirus Vaccines
- Interventions
- Project Voice; HPV Informational Video
- Participants
- 22
- Sites
- 1
- Countries
- United States
Trials that died the same way
- A Study of Retreatment With Brentuximab Vedotin in Subjects With Classic Hodgkin Lymphoma or CD30-expressing Peripheral T Cell Lymphoma
“Study stopped early due to low patient accrual.” - Using Fostamatinib to Treat Post-Hematopoietic Stem Cell Transplant Immune-mediated Cytopenias
“Clinical trial was halted prematurely due to low enrollment” - Comparison of Efficacy of Behavioral Approaches for Treatment of Insomnia
“Study halted prematurely and will not resume; participants are no longer being examined or receiving intervention. COVID Complications.” - Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b Chronic Hepatitis C Virus (HCV) Infection With End Stage Renal Disease (ESRD) on Hemodialysis (HD)
“Study halted prematurely, prior to enrollment of first participant” - High Cut Off Dialysis in Systemic Inflammatory Response Syndrome Patients After Cardiac Surgery
“Study halted prematurely, prior to enrollment of first patient, due to recruiting problems.”
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.