Trial · NCT00733343
Registered outcomes42
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 20 of 42
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | All Cause Mortality or Unplanned Hospitalisation/Prolongation of Hospitalisation for Worsening Heart Failure | time to first event, assessed for up to 70 weeks | |
| Primary | Cardiovascular Mortality or Unplanned Hospitalisation/Prolongation of Hospitalisation for Worsening Heart Failure | time to first event, assessed for up to 70 weeks | |
| Primary | All Cause Mortality or All Cause Unplanned Hospitalisation/Prolongation of Hospitalisation | time to first event, assessed for up to 70 weeks | |
| Secondary | Death From Any Cause | the last follow up or at the last available observation within Follow Up (FU), assessed for up to 70 weeks | |
| Secondary | Non-cardiovascular Death | the last follow up or at the last available observation within FU, assessed for up to 70 weeks | |
| Secondary | Cardiovascular Death | the last follow up or at the last available observation within FU, assessed for up to 70 weeks | |
| Secondary | Unplanned Hospitalisation/Prolongation of Hospitalisation Due to Worsening of Heart Failure | the last follow up or at the last available observation within FU, assessed for up to 70 weeks | |
| Secondary | Unplanned Hospitalisation/Prolongation of Hospitalisation for Other Reasons or Death | the last follow up or at the last available observation within FU, assessed for up to 70 weeks | |
| Secondary | Adequate Shock in Patients With ICD (Evaluation of Appropriateness Will Also be Made by the Endpoint Review Committee, ERC), Long-Term Atrial Defibrillator Insertion or Cardiovascular Death | the last follow up or at the last available observation within FU, assessed for up to 70 weeks | |
| Secondary | First Survived Resuscitation for Any Reason (Evaluation Will Also be Made by the ERC) | the last follow up or at the last available observation within FU, assessed for up to 70 weeks | |
| Secondary | First Survived Resuscitation of Sudden Cardiac Arrest (Evaluation Will Also be Made by the ERC) | the last follow up or at the last available observation within FU, assessed for up to 70 weeks | |
| Secondary | Age Baseline | 1 x at Baseline | |
| Secondary | Body Weight Baseline | 1 x at baseline | |
| Secondary | Body Mass Index (BMI) Baseline | 1 x baseline | |
| Secondary | Left Ventricular Ejection Fraction at Baseline | 1x at baseline | |
| Secondary | Blood Pressure Systolic Baseline | 1 x at baseline | |
| Secondary | Blood Pressure Diastolic Baseline | 1 x at baseline | |
| Secondary | Hemoglobine Baseline | 1 x at baseline | |
| Secondary | Creatinine Baseline | 1 x at baseline | |
| Secondary | Glomerular Filtration Rate Baseline | 1 x at baseline |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT00733343/registered