Autopsy report · NCT07429591
Risk Screening & Primary Prevention of Elder Abuse in People Living With Dementia
Cause of deathRegulatory or ethics
“Study paused per IRB request.”
Life of this trial
- Registered 3 months before it started.
- Suspended: paused, and may or may not restart.
- 1,000 participants planned (an estimate, not an actual count).
Vital statistics
- Status
- Suspended
- Phase
- Na
- Sponsor
- University of Southern California
- Sponsor type
- University, hospital or other
- Conditions
- Caregivers of Alzheimer's Disease or Memory Problem Patients; Caregiver Wellbeing; Elder Abuse
- Interventions
- Risk Assessment Screening; Coach and Website Intervention
- Participants
- 1,000 (planned, not actual)
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Clinical Data Collection for Obstetric Ultrasound Algorithms
“Study paused temporarily pending IRB approval of an amendment to the protocol and consent form.” - Simvastatin Nasal Rinses for the Treatment of COVID-19 Mediated Dysomsia
“Study halted prematurely; IRB approval not obtained” - A Quality of Life Study Using Insulin Potentiation Targeted LowDose (IPTLD) Chemotherapy and Nutrition Therapy in the Treatment of Cancer
“The IRB which was overseeing the study stopped overseeing it” - Pilot Study of Alternative Treatments of Unexplained Chronic Fatigue
“IRB ended and NIH study ended” - Methadone as an Alternative Treatment for Children Underdoing HSCT
“Study is closed with the IRB due to no funding. May resume once funding is obtained.”
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.