Autopsy report · NCT00944125
Dual Site Left Ventricular (LV) Pacing
Cause of deathStaffing, sites or logistics
“for administrative reasons (no safety concerns), no analysis completed”
Life of this trial
- Registered 1 month after it had already started.
- Ran for about 4 years 1 month before it stopped.
- 50 participants enrolled.
- Results were posted on the registry 2 years 8 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Wake Forest University Health Sciences
- Sponsor type
- University, hospital or other
- Conditions
- Congestive Heart Failure; LV Dysfunction
- Interventions
- Dual Site LV Pacing; BiV Pacing
- Participants
- 50
- Sites
- 2
- Countries
- United States
Trials that died the same way
- Preoperative Use of Darifenacin (Enablex) to Alleviate Postoperative Ureteral Stent Pain
“Co-Investigator left institution. No data analysis occurred.” - Evaluation of Alcon Ladarvision Wavefront-Guided PRK
“Lack of resources and not because of any concern with the safety or effectiveness of the procedures studied.” - Efficacy, Safety, Tolerability and Pharmacokinetics of SUN13837 to Treat Acute Stroke
“study was stopped for business/administrative reasons and not for patient safety concerns” - Effectiveness and Safety Study of Pentosan Polysulfate Sodium for the Treatment of Interstitial Cystitis
“Interim Analysis showed that study continuation was futile. No safety concerns were raised during the trial.” - Safety and Tolerability of PNT001 in Patients With Acute Traumatic Brain Injury (TBI)
“The study was terminated due to administrative, non-safety related reasons.”
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.