Autopsy report · NCT03504033
Xenon-anesthesia on Patients Undergoing Major Liver-resection
Cause of deathFunding or business
“A device would have had to be maintained. The maintenance company is insolvent; both another maintenance company and another serviced device were not available.”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 4
- Sponsor
- RWTH Aachen University
- Sponsor type
- University, hospital or other
- Conditions
- Liver Function After Partial Liver Resection
- Interventions
- Xenon; Desflurane
- Participants
- 0
- Sites
- 1
- Countries
- Germany
Trials that died the same way
- Effect of T6 Dermatome Electrical Stimulation on Gastroduodenal Motility in Healthy Volunteers
“Electrical device malfunction; recruitment was stopped.” - Stomaplasty Ring (KoringTM) for Prevention of Parastomal Hernia
“The device used was removed from the market” - Indirect Calorimetry: SensorMedics Vmax vs GE Carescape - a Method Comparison Study
“Equipment failure”
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.