Autopsy report · NCT05112575

Evaluation of Patient Stress Level Caused by Radiological Investigations in Early Postoperative Phase After Craniotomy

“Failed resources.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 1 year after it had already started.
• Ran for about 2 years 4 months before it stopped.
• 152 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

University of Zurich

Sponsor type

University, hospital or other

Conditions

Postoperative Pain; Postoperative Nausea

Interventions

Postoperative imaging with magnetic resonance imaging or computed tomography

Participants

152

Sites

1

Countries

Switzerland

Trials that died the same way

• Prediction of Expected Length of Hospital Stay Using Machine Learning
  “Insufficient resources.” (74% match in meaning)
• A Challenge Study to Assess the Blood-stage Efficacy of Full-length SUM-101 Malaria Vaccine Candidate
  “Not enough resources” (71% match in meaning)
• Chronic Pain, Couples, & Physical Activity
  “Resources not available.” (69% match in meaning)
• Study on the Use of Intraoperative Neurophysiological Monitoring in Spinal Cord Stimulator Trials
  “lack of resources” (68% match in meaning)
• Regorafenib in Combination With Venetoclax and Azacitidine for the Treatment of Patients With Relapsed or Refractory Acute Myeloid Leukemia
  “resources” (68% 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.