Autopsy report · NCT02724189

The Evaluation of MyPreOp, an Online Preoperative Assessment Tool

“Lack of logistic capabilities at the study site”

The sponsor’s own words in the registry.

Life of this trial

• Ran for about 2 months before it stopped.
• 200 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

Michelle Cole

Sponsor type

University, hospital or other

Conditions

Focus of Study: The Safety of an Online Pre-assessment Tool

Interventions

MyPreOp assessment; Nurse led assessment

Participants

200

Trials that died the same way

• PK Intravenous Lidocaine Infusion
  “Lack of available study participants.” (71% match in meaning)
• Thoracic Kyphosis and Osteoporosis: Study of Their Relationship With Respiratory Functions in Chronic Obstructive Pulmonary Disease.
  “The site is no more able to conduct the study” (69% match in meaning)
• Ibuprofen Versus Acetaminophen for Treatment of Mild Traumatic Brain Injury
  “Lack of study participants.” (67% match in meaning)
• Altruistic Decisions
  “Insufficient on-site staff to manage study” (67% match in meaning)
• HBOT Late Radiation Tissue Injury
  “Lack of resources to complete the study” (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.