Autopsy report · NCT01691443

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.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 9 months before it started.
• Ran for about 1 year 11 months before it stopped.
• 1 participant enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

University Hospital, Grenoble

Sponsor type

University, hospital or other

Conditions

Sensory Deficit

Interventions

pressure sensor and wrist shaker, not marked CE, developped by Texisense

Participants

1

Sites

1

Countries

France

Trials that died the same way

• Continuous Glucose Monitoring (POC) in the ICU
  “Study device required infeasible modifications. No patients received device.” (66% match in meaning)
• 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” (64% match in meaning)
• Immunomagnetic Detection of Cancer Cells in Pleural Effusion in Lung Cancer Patients as Additional Staging and Prognostic Tool
  “Technical problems with the device” (64% match in meaning)
• Electrode Placement and Audiologic Outcomes With the Advanced Bionics HiFocus L23 Electrode
  “device under study complication-due to PI departure, study closed and will not reopen” (61% match in meaning)
• Gynecare TVT Secur for the Management of Stress Urinary Incontinence (SUI)
  “Study design required a change in device” (61% 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.