Trial · NCT01676285
Metoprolol Succinate in Cardiac Remodeling Related to Cirrhosis
NCT01676285, Phase 3, Completed, University of Sao Paulo
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Metoprolol Succinate in Cardiac Remodeling Related to Cirrhosis. Trials, record NCT01676285. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01676285
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Metoprolol Succinate in Cardiac Remodeling Related to Cirrhosis
- NCT number
- NCT01676285
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 125 participants, actual
- Lead sponsor
- University of Sao Paulo
- Conditions
- Cirrhosis, Cirrhotic Cardiomyopathy, Cardiac Remodeling
- Interventions
- Metoprolol succinate, placebo
- First posted
- 2012-08-30
- Last updated
- 2014-09-11
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Improvement of systolic function | six months | Systolic functional reserve is measured by aortic velocity time integral in echocardiographic at rest and stress with dobutamine. |
| Secondary | Improvement in left ventricular diastolic function | six months | |
| Secondary | Renal function | From randomization until six months | |
| Secondary | Serum level of BNP, catecholamines, plasmatic renin activity | Six months | |
| Secondary | Mortality | From randomization until six months of follow up | |
| Secondary | Quality of life | Six months | |
| Secondary | Electrophysiologic modifications | Six months | QT prolongation R-R variability |
Source ClinicalTrials.gov
Outcomes0
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/NCT01676285
GET https://conductscience.org/api/trials/v1/NCT01676285/registered