Autopsy report · NCT00337116
Intravenous Isosorbide Dinitrate Versus Sublingual Isosorbide Dinitrate for the Relief of Acute Anginal Episodes in Acute Coronary Syndrome (ACS) Patients
Cause of deathStaffing, sites or logistics
“LOGISTIC DIFFICULTIES”
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- Withdrawn before it enrolled anyone.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- Withdrawn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
- Phase 4
- Sponsor
- Soroka University Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Unstable Angina; Myocardial Infarction
- Interventions
- iso sorbide dinitrate iv bolus or s/l
- Participants
- 80 (planned, not actual)
- Sites
- 1
- Countries
- Israel
Trials that died the same way
- PNE Plus Exercise Versus Exercise for Chronic Rotator Cuff Tendinopathy
“Logistic issues” - A Single-center Study Designed to Evaluate the Safety and Efficacy of Tulipon
“logistic and financial issues.” - Acute Haemodynamic Impact of an IV Glucose-injection
“never started due to logistic issues” - Monitoring and Evaluation of a Cognitive Behavioral Therapy Program Focused on Attention and Emotion Regulation for Children With Fetal Alcohol Spectrum Disorder
“logistic problem and absence of coordinating Investigator”
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.