Autopsy report · NCT03672370
PMCF Study on the Safety and Performance of the Alloclassic Variall Cup Ceramic Bearing System in Total Hip Arthroplasty
Cause of deathFunding or business
“Study terminated as CE marks of the devices used have not been renewed.”
Life of this trial
- Registered 3 years 6 months after it had already started.
- Ran for about 5 years 1 month before it stopped.
- 100 participants enrolled.
- Results were posted on the registry 8 months after it ended.
Vital statistics
- Status
- Terminated
- Sponsor
- Zimmer Biomet
- Sponsor type
- Industry
- Conditions
- Avascular Necrosis; Osteoarthritis; Inflammatory Arthritis; Posttraumatic Arthritis
- Participants
- 100
- Sites
- 2
- Countries
- Austria
Trials that died the same way
- A Real-World Study in Patients With HR+/HER2- Advanced Breast Cancer
“Due to a strategic decision by the company, the study will not proceed, and no subjects have been enrolled to date.” - The ENABLE Study: Safety and Efficacy Study of INZ-701 in Patients With ENPP1 Deficiency
“Study was not initiated as it is no longer consistent with the Sponsor's development plans.” - A Safety Study of IV Stem Cell-derived Extracellular Vesicles (UNEX-42) in Preterm Neonates at High Risk for BPD
“The study was discontinued due to a business decision; no safety concerns were noted.” - Erwinase for Patients With Relapsed/Refractory Acute Lymphoblastic Leukemia (ALL) (IND 104224)
“Study was terminated due to lack of accrual.” - Utility of Hyperpolarized 13C-pyruvate Metabolic Magnetic Resonance Imaging
“"Study terminated due to institutional resource constraints, including limited availability of specialized equipment and technical support. Termination was not related to participant safety, data quality, study conduct, or the investigational product”
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.