Autopsy report · NCT01273428

HP011-101, HP828-101, and Standard Care for Pressure Ulcers

“The device test article is no longer available”

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• Withdrawn before it enrolled anyone.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Withdrawn

Phase

Phase 2

Sponsor

Healthpoint

Sponsor type

Industry

Conditions

Pressure Ulcers

Interventions

HP011-101; HP-828-101; Standard Care

Participants

0

Trials that died the same way

• Non-Invasive Measurement of Cardiac Output and Stroke Volume in PE
  “Study device no longer available” (68% match in meaning)
• Increasing Bone Density by Application of Surface Electrical Stimulation
  “Device is not available.” (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” (65% match in meaning)
• Distal Versus Proximal Protection on Cerebral Microembolization During High-risk Carotid Artery Stenting
  “device unavailable” (59% 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.