Autopsy report · NCT02656628

Observational Patient Registry of the Dynamic Locking Screws

“Due to the voluntary recall of the study device (DLS 3.7mm and DLS 5.0mm)”

The sponsor’s own words in the registry.

Life of this trial

• Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.

Vital statistics

Status

Withdrawn

Sponsor

Synthes GmbH

Sponsor type

Industry

Conditions

Proximal or Diaphyseal Humerus Fracture; Diaphyseal or Distal Femur Fracture; Diaphyseal, Distal or Proximal Tibia Fracture

Interventions

Dynamic Locking Screw 3.7mm and 5.0mm

Participants

0

Sites

1

Countries

Australia

Trials that died the same way

• Real-time Tumor Localization and Guidance for Radiotherapy Using Ultrasound (US) and Magnetic Resonance (MR)
  “Device to be used in study is no longer available” (61% match in meaning)
• An in Vivo Comparison of the Debridement Efficiency of Needle Irrigation Versus Ultrasonic Irrigation
  “Manufacturer changed device so no study will be done; ie it was never started” (60% match in meaning)
• Non-Invasive Measurement of Cardiac Output and Stroke Volume in PE
  “Study device no longer available” (58% match in meaning)
• Functional Assessment of a Vibration Feedback on the Gripping Pressure in the Territory of the Median Nerve
  “Technical problem with one of the medical device used for the study.” (57% match in meaning)
• Continuous Glucose Monitoring (POC) in the ICU
  “Study device required infeasible modifications. No patients received device.” (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.