Trial · NCT07898345
Prognostic Value of Functional-Nutritional Status in Older Adults With Acute Coronary Syndrome
NCT07898345, Not yet recruiting, Samara State Medical University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Prognostic Value of Functional-Nutritional Status in Older Adults With Acute Coronary Syndrome. Trials, record NCT07898345. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07898345
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Prognostic Value of Functional-Nutritional Status in Older Adults With Acute Coronary Syndrome
- NCT number
- NCT07898345
- Status
- Not yet recruiting
- Enrollment
- 270 participants, estimated
- Lead sponsor
- Samara State Medical University
- Conditions
- Acute Coronary Syndromes (ACS)
- Interventions
- Functional-Nutritional Burden
- First posted
- 2026-10-27
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes26
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to First Major Adverse Clinical Event | From baseline (t0) through day 365 | Time from baseline (t0) to the first of: all-cause death, nonfatal myocardial infarction, ischemic stroke, or unplanned cardiovascular rehospitalization. Nonfatal myocardial infarction is a new myocardial infarction after and distinct from the index event (after index unstable angina, including a first-ever myocardial infarction). Participants without an event are censored at the last date through which the absence of events was confirmed from verified sources, and no later than day 365. |
| Secondary | All-Cause Mortality | From baseline (t0) through day 365 | Death from any cause. The date of death will be established from available medical or other authorized records; the number of deaths and time to death will be assessed. |
| Secondary | Cardiovascular Mortality | From baseline (t0) through day 365 | Death due to a documented cardiovascular cause; a subcategory of all-cause death, not an additional component of the primary composite. Deaths of unknown cause are not classified as cardiovascular and are reported separately. |
| Secondary | Nonfatal Myocardial Infarction | From baseline (t0) through day 365 | A new nonfatal myocardial infarction after and distinct from the index acute coronary syndrome event (after index unstable angina, including a first-ever myocardial infarction), confirmed by medical documentation; reinfarction (within 28 days of the index event) and recurrent infarction (after 28 days) are recorded separately. Number of participants with an event. |
| Secondary | Ischemic Stroke | From baseline (t0) through day 365 | Acute focal neurological deficit of ischemic origin confirmed by CT or MRI (if imaging is not possible, by a neurologist's conclusion). Number of participants with an event. |
| Secondary | Unplanned Cardiovascular Rehospitalization | From discharge after the index hospitalization through day 365 after t0 | A new unplanned admission after the end of the continuous index hospitalization for acute coronary syndrome, acute or decompensated heart failure, cardiogenic shock, clinically significant arrhythmia or conduction disorder, or urgent repeat revascularization; transfers within one episode, planned (including staged) admissions and day-hospital care are not counted. Number of participants with an event. |
| Secondary | All-Cause Death or Nonfatal Myocardial Infarction | From baseline (t0) through day 365 | Time to the first occurrence of all-cause death or a nonfatal myocardial infarction after the index acute coronary syndrome episode. |
| Secondary | Acute Heart Failure During Index Hospitalization | Up to 365 days (duration of the index hospitalization, from hospital admission to discharge or in-hospital death) | Occurrence of acute heart failure documented during the index admission for acute coronary syndrome; number and proportion of participants affected. Events are recorded from medical documentation for the whole index admission; events occurring after baseline (t0) are reported separately. |
| Secondary | Cardiogenic Shock During Index Hospitalization | Up to 365 days (duration of the index hospitalization, from hospital admission to discharge or in-hospital death) | Occurrence of cardiogenic shock documented during the index admission; number and proportion of participants affected. Events are recorded from medical documentation for the whole index admission; events occurring after baseline (t0) are reported separately. |
| Secondary | Life-Threatening Arrhythmia During Index Hospitalization | Up to 365 days (duration of the index hospitalization, from hospital admission to discharge or in-hospital death) | Occurrence of a documented life-threatening arrhythmia during the index admission, including ventricular tachycardia or ventricular fibrillation; number and proportion of participants affected. Events are recorded from medical documentation for the whole index admission; events occurring after baseline (t0) are reported separately. |
1 to 10 of 26Source ClinicalTrials.gov
See all 26 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07898345
GET https://conductscience.org/api/trials/v1/NCT07898345/registered?page=2