Autopsy report · NCT04855370

Non-Invasive Measurement of Cardiac Output and Stroke Volume in PE

“Study device 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• Withdrawn before it enrolled anyone.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Withdrawn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

Na

Sponsor

University of California, Los Angeles

Sponsor type

University, hospital or other

Conditions

Pulmonary Embolism; Pulmonary Embolus/Emboli; Pulmonary Disease; Pulmonary Embolism and Thrombosis; Pulmonary Embolism Subacute Massive; Pulmonary Embolism Acute Massive

Interventions

Non-invasive hemodynamic measurements

Participants

0

Sites

1

Countries

United States

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” (94% match in meaning)
• Assessing the Comparability of 2D and 4D Ultrasound Measurements
  “Equipment to run the study was not available” (73% 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” (72% match in meaning)
• HP011-101, HP828-101, and Standard Care for Pressure Ulcers
  “The device test article is no longer available” (68% 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” (66% 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.