Autopsy report · NCT03003338
MHH-HCV-NPM-Neuropsychiatric Manifestations of HCV-infection During and After Treatment With OBV/PTV/r and DSV
Cause of deathSlow enrollment, also staffing, sites or logistics
“The recruitment was stopped prematurely by the sponsor in accordance with the principal investigator because of the difficulties to recruit patients and to achieve the planned numbers of patients within a reasonable time frame.”
Life of this trial
- Registered 1 year 3 months before it started.
- Ran for about 1 year before it stopped.
- 5 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Hannover Medical School
- Sponsor type
- University, hospital or other
- Conditions
- Hepatitis C, Chronic
- Interventions
- OBV/PTV/r and DSV; Placebo to match OBV/PTV/r and DSV
- Participants
- 5
- Sites
- 1
- Countries
- Germany
Trials that died the same way
- The Performance and Safety of Petit Drill in the French Paediatric Population: a Post-market Clinical Follow-up Study
“Due to difficulty in recruiting patients, the Sponsor decided to prematurely stop the study” - 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.” - Platelet Reactivity With Fentanyl, Morphine, or no Narcotic
“The study was halted prematurely due to difficulties in recruiting a sufficient number of participants. Despite efforts to enroll eligible individuals, the recruitment goals were not met, making it infeasible to continue the study as planned.” - Predictive Value of Pre-TAVI Infrahissian Conduction Time in the Occurrence of Complete Atrioventricular Block
“The sponsor, in consultation with the coordinating investigator, had decided to stop enrolment prematurely because the enrolment rate would not have made it possible to reach the target of 142 patients without increasing the duration of the study” - Omission of Surgery in Clinically Low-risk HER2positive Breast Cancer With High HER2 Addiction and a Complete Response Following Standard Anti-HER2-based Neoadjuvant Therapy
“The study was prematurely halted primarily due to low patient accrual. Despite efforts to optimize recruitment, the enrollment rate remained insufficient to meet the predefined targets, and continuation was deemed unfeasible”
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.