Autopsy report · NCT04727060
Open Label Study to Collect Clinical Data to Document Clinical Performance and Safety in Total Knee Arthroplasty
Cause of deathRegulatory or ethics
“the clinical data collected to date are sufficient for regulatory requirements”
Life of this trial
- Registered 8 years 11 months after it had already started.
- Ran for about 11 years 11 months before it stopped.
- 2,146 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Corin
- Sponsor type
- Industry
- Conditions
- Total Knee Arthroplasty; Knee Disease; Total Knee Replacement; Osteo Arthritis Knee
- Interventions
- patient with knee arthroplasty
- Participants
- 2,146
- Sites
- 1
- Countries
- France
Trials that died the same way
- Study to Evaluate Long Term Performance and Safety of the Knee Prosthesis (HLS KneeTec Deep Dish)
“the clinical data collected to date is sufficient for regulatory requirements” - Pilot Study Of Anti-Programmed Death Ligand-1 (Anti-PD-L1, Atezolizumab) In Asymptomatic Myeloma
“Based on FDA requirements” - Novel Interventions in HIV-1 Infection
“Data from the 12 patients recruited has now been analysed, and it has been determined that it is sufficient to meet the study objectives.” - Craniomaxillofacial Allotransplantation
“It was determined that the study would be integrated into the standard clinical care.” - DB289 Versus TMP-SMX for the Treatment of Acute Pneumocystis Jiroveci Pneumonia (PCP)
“FDA Clinical Hold as of 12/21/07 due to safety concerns”
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.