Autopsy report · NCT01082965
Acute Effects Of Donepezil On Brain Perfusion And Memory In Subjects With Cognitive Impairment And Mild Alzheimer's Disease
Cause of deathSlow enrollment
“The study was terminated because of slow enrollment. The decision to terminate the trial was not based on any safety or efficacy concerns.”
Life of this trial
- Registered 5 months before it started.
- Ran for about 2 years before it stopped.
- 18 participants enrolled.
- Results were posted on the registry 1 year 2 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Pfizer
- Sponsor type
- Industry
- Conditions
- Alzheimer's Disease
- Interventions
- Donepezil; Placebo
- Participants
- 18
- Sites
- 8
- Countries
- United States
Trials that died the same way
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“The study was terminated due to lower than expected enrollment. The decision to terminate the study was not based on any safety or efficacy concerns.” - Evaluation of the Clinical and Economic Impact of painPRIMER in the Treatment of Low Back Pain in a Primary Care Setting
“The study was terminated on 02-Jun-2014 due to slow enrollment. The study was not terminated for reasons of either safety or efficacy.” - A Study to Learn About the Effect of Avelumab First-Line Maintenance in Canadian People With Advanced Bladder Cancer
“The trial was terminated for strategic reasons. The decision was not based on any safety and/or efficacy concerns.” - Study Assessing the Efficacy and Safety of Alpelisib + Nab-paclitaxel in Subjects With Advanced TNBC Who Carry Either a PIK3CA Mutation or Have PTEN Loss
“The study was terminated following a strategic decision to halt recruitment due to persistently slow enrollment. This decision was not driven by any new or unexpected safety concerns.” - An Open-Label, Randomized, Multicenter Trial of Encorafenib + Binimetinib Evaluating a Standard-dose and a High-dose Regimen in Patients With BRAFV600-mutant Melanoma Brain Metastasis
“Study terminated due to lack of enrollment of the target population. There were no safety, efficacy, or regulatory interaction involved in the decision to stop enrollment.”
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.