Autopsy report · NCT02820766
Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting
Cause of deathStaffing, sites or logistics
“Logistics of study did not allow for consistent data collection”
Life of this trial
- Registered 3 months before it started.
- Ran for about 7 months before it stopped.
- 22 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Smith & Nephew, Inc.
- Sponsor type
- Industry
- Conditions
- Osteoarthritis; Degenerative Arthritis; Traumatic Arthritis
- Participants
- 22
- Sites
- 3
- Countries
- United States
Trials that died the same way
- Tricyclic Antidepressants (TCAs) on Gastric Emptying
“Futility; study coordinator left and were unable to continue data collection; missing data” - Philadelphia Immediate Transport in Penetrating Trauma Trial
“The study was not feasible due to logistical elements” - Recurrent Abdominal Pain and Exocrine Pancreatic Insufficiency
“Data collection discontinuity and sponsor reallocation of study resources to manufacturing” - Azithromycin for Severe Acute Malnutrition in CMAM, Nigeria
“Study was halted due to low follow-up rates and issues with data collection” - Intraoperative Methadone Administration for Improved Pain Control in Spinal Fusion Patients
“Due to personnel loss and logistical issues the study was unable to be completed as planned.”
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.