Autopsy report · NCT05497206

ROSA® Hip System THA PMCF

“The data needed for regulatory submissions based on the current pace of the study, will not be available in the foreseeable future.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 2 years 3 months before it started.
• Ran for about 6 months before it stopped.
• 12 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

Zimmer Biomet

Sponsor type

Industry

Conditions

Osteoarthritis, Hip; Avascular Necrosis of Hip

Interventions

One of the following hip implants may be used within this arm of the study: G7 Acetabular System, Taperloc Complete System, Avenir and Avenir Complete Systems, and Echo Bi-Metric System

Participants

12

Sites

2

Countries

United States

Trials that died the same way

• A Phase III Study of Re-Irradiation in Recurrent Glioblastoma
  “This study will not be proceeding due to lack of funding from anticipated sources” (61% match in meaning)
• A Study of Montelukast (MK-0476) Compared With Fluticasone in Pediatric Participants With Chronic Asthma (MK-0476-303)
  “Based on input from regulatory agencies, it is not necessary to conduct this study. An ongoing study was sufficient for regulatory purposes.” (61% match in meaning)
• Immunomonitoring and Biomarker Research in Patients With Squamous Cell Anal Carcinoma
  “Study not submitted to regulatory authorities” (60% match in meaning)
• Randomized Controlled Clinical Outcomes of the Vanguard XP Bicruciate Knee System
  “Data no longer required to meet regulatory requirements.” (59% match in meaning)
• Study of Body Composition Methodology in Young Children (InfantPod)
  “This study will not be conducted. A new study is replacing this one.” (57% match in meaning)

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.