Autopsy report · NCT07043556
Assessment of Artificial Intelligence Algorithms for ROTEM
Cause of deathSlow enrollment
“The study was stopped because it was considered unlikely that the required number of patients could be prospectively recruited across the participating study centers.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Sponsor
- Ondokuz Mayıs University
- Sponsor type
- University, hospital or other
- Conditions
- Coagulopathy
- Interventions
- Artificial Intelligence-Based ROTEM Interpretation
- Participants
- 0
- Sites
- 2
- Countries
- Turkey (Türkiye)
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“The study stopped because patient enrollment requirements were not met.” - The Performance and Safety of Petit Drill in the French Paediatric Population: a Post-market Clinical Follow-up Study
“Due to difficulty in recruiting patients, the Sponsor decided to prematurely stop the study” - Omission of Surgery in Clinically Low-risk HER2positive Breast Cancer With High HER2 Addiction and a Complete Response Following Standard Anti-HER2-based Neoadjuvant Therapy
“The study was prematurely halted primarily due to low patient accrual. Despite efforts to optimize recruitment, the enrollment rate remained insufficient to meet the predefined targets, and continuation was deemed unfeasible” - The Role of Osteopathic Manipulative Medicine in Recovery From Concussions
“Due to lower than anticipated enrollment number, this study was stopped.”
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.