Autopsy report · NCT02844127
Effect of Right Ventricular Lead Position on Defibrillation Threshold
Cause of deathOther
“Devices proposed for use in the protocol no longer used by physician”
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- Withdrawn before it enrolled anyone.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- Withdrawn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
- Na
- Sponsor
- OhioHealth
- Sponsor type
- University, hospital or other
- Conditions
- Ventricular Tachycardia; Ventricular Fibrillation
- Interventions
- Implantable Cardioverter Defibrillator (ICD)
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Impact of Current Smoking in the Tolerance of Bronchoscopy
“the physician responsable for this protocol left our hospital” - Vaccines and Dietary Oats in the Treatment of Ulcerative Colitis
“Lack of patients compatible with the protocol´s criteria” - Continuous Glucose Monitoring (POC) in the ICU
“Study device required infeasible modifications. No patients received device.” - Study of Adoptive Immunotherapy in Relapsed and Non-resectable Sarcomas After Multimodal Treatment.
“Initial version of the protocol not submitted and new version approved has a new sponsor and it has been added into Clinicaltrials by the new sponsor” - Intermittent Theta Burst Stimulation for MDD
“Protocol discontinued for futility”
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.