Autopsy report · NCT03289754

A Prospective Study to Evaluate the iTotal Knee and iPoly XE Tibial Inserts

Cause of deathOther Automatic label, confidence 0.3, unverified. How labels are made.

“Decision of investigational team”

The sponsor’s own words in the registry.

Life of this trial

Registered 4 months before it started.
Ran for about 4 years 5 months before it stopped.
52 participants enrolled.
Results were posted on the registry 3 years 4 months after it ended.

Vital statistics

Status: Terminated
Phase: Na
Sponsor: Restor3D
Sponsor type: Industry
Conditions: Knee Osteoarthritis
Interventions: iPoly XE tibial insert with ConforMIS iTotal KRS
Participants: 52
Sites: 1
Countries: Germany

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.