Autopsy report · NCT03460015
Sevoflurane in Chronic Obstructive Pulmonary Disease Exacerbation
Cause of deathStaffing, sites or logistics
“Study halted prematurely and will not resume; participants are no longer being examined or receiving intervention The study was terminated prematurely due to inclusion difficulties”
Life of this trial
- Registered 1 month before it started.
- Ran for about 2 years 9 months before it stopped.
- 16 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- University Hospital, Montpellier
- Sponsor type
- University, hospital or other
- Conditions
- COPD Exacerbation; Invasive Mechanical Ventilation
- Interventions
- Sevoflurane; Propofol
- Participants
- 16
- Sites
- 1
- Countries
- France
Trials that died the same way
- Comparison of Efficacy of Behavioral Approaches for Treatment of Insomnia
“Study halted prematurely and will not resume; participants are no longer being examined or receiving intervention. COVID Complications.” - Leronlimab (PRO 140) Combined With Carboplatin in Patients With Cytokine Chemokine Receptor 5 Positive (CCR5+) mTNBC
“Study terminated prematurely due to business reasons. Participants are no longer examined or receiving intervention.” - Secukinumab for NLD (Cosentyx) in Patients With Necrobiosis Lipoidica Diabeticorum (NLD)
“Study halted prematurely due COVID-19 pandemic and did not resume; participants are no longer being examined or receiving intervention.” - Function, Pain, and Alignment Following Knee Replacement for the Treatment of Osteoarthritis
“The study was prematurely terminated due to a long pause in study activities and significant missing participant data.” - Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b Chronic Hepatitis C Virus (HCV) Infection With End Stage Renal Disease (ESRD) on Hemodialysis (HD)
“Study halted prematurely, prior to enrollment of first participant”
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.