Trial · NCT05708053
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postprocedural myocardial injury | 6 months | the occurrence of postprocedural myocardial injury, defined as a postprocedural elevation of CKMB or cTnI more than 1 times the 99 th percentile of the URL \[ 24 hours post PCI\] |
| Secondary | CK-MB | 24 hours post PCI | Mean peak values of CK-MB after intervention |
| Secondary | cTn | 24 hours post PCI | Mean peak values of cTnI after intervention |
| Secondary | LVEF in percent | Baseline- 6 months | Echo: to measure LVEF in percent |
| Secondary | LVMI in g/m2 | Baseline- 6 months | left ventricular mass index (LVMI) will be calculated in g/m2 using the sex and body surface area (m²) and measures of LVEDD in mm, IVSd in mm, PWd from the measures in the echocardiography |
| Secondary | GFR | Baseline- monthly- 6 months | glomerular filtration rate (GFR) will be calculated (unit ml/min) using age in years, sex, body weight in kilograms and serum creatinine in mg/dL |
| Secondary | Serum creatinine (SCr) | Baseline- monthly- 6 months | Serum creatinine (SCr) in mg/dL |
| Secondary | Lactate concentration | Baseline - 6 months | lactate concentration unit in mmol/L |
| Secondary | Glucometabolic State | Baseline - 6 months | Glucometabolic State using HbA1c (unit mmols/mol) |
| Secondary | Incidence of Cardiovascular Event | Baseline - 6 months | Cardiovascular events including major cardiac adverse events (MACE; death, recurrent MI, target lesion revascularization), stroke, non-elective hospitalizations for chest pain or heart failure, all recurrent coronary interventions, and internal cardiac defibrillator implantations. Mortality will be divided into cardiac and non- cardiac. Cardiac death will be divided into three categories: heart failure, sudden death, and others. |
| Secondary | Rate of hospitalization | through study completion, an average of 6 months | The number of hospitalizations within each group will be calculated during the study period. |
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/NCT05708053/registered