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Trial · NCT02147834

Effectiveness of Ranolazine on Reducing Chest Pain in Patients With Blockage But no Stents

NCT02147834, Phase 2, Terminated, North Florida Foundation for Research and Education; results first posted 2019-06-11

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effectiveness of Ranolazine on Reducing Chest Pain in Patients With Blockage But no Stents. Trials, record NCT02147834. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02147834

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Effectiveness of Ranolazine on Reducing Chest Pain in Patients With Blockage But no Stents
NCT number
NCT02147834
Status
Terminated
Phases
Phase 2
Enrollment
5 participants, actual
Lead sponsor
North Florida Foundation for Research and Education
Conditions
Angina
Interventions
Ranolazine, Sugar pill
First posted
2014-05-28
Last updated
2019-06-11
Results first posted
2019-06-11

Source ClinicalTrials.gov

Registered outcomes3

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimarySeattle Angina Questionnaire Score Change From Baseline to Month 4Change in baseline to month 4
The Seattle Angina Questionnaire is a valid and reliable instrument that measures five clinically important dimensions of health in patients with coronary artery disease (physical limitation, anginal stability, anginal frequency, treatment satisfaction, and disease perception).
SecondarySubjective Well BeingCompare from baseline to month 4overall feeling of well being determined from rating of excellent, good, fair or poor at baseline compared to same at month 4
SecondaryIschemia Driven Revascularization or Hospitalization4 monthfrequency of the number of reported adverse events for ischemia driven revascularization or hospitalization

Outcomes3

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYSeattle Angina Questionnaire Score Change From Baseline to Month 4Change in baseline to month 4The investigator ended this project early due to futility. Do data was analyzed.
SECONDARYSubjective Well BeingCompare from baseline to month 4The investigator ended this study early due to futility. no data was analyzed.
SECONDARYIschemia Driven Revascularization or Hospitalization4 monthThe investigator ended this study early due to futility. No data was analyzed.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDRanolazine3
Overall StudySTARTEDSugar Pill2
Overall StudyCOMPLETEDRanolazine3
Overall StudyCOMPLETEDSugar Pill2
Overall StudyNOT COMPLETEDRanolazine0
Overall StudyNOT COMPLETEDSugar Pill0

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityRanolazine
Total, all-cause mortalitySugar Pill
Total, other adverse eventsRanolazine03
Total, other adverse eventsSugar Pill02
Total, serious adverse eventsRanolazine03
Total, serious adverse eventsSugar Pill02

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 comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Ranolazine vs Sugar Pill: serious adverse events

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT02147834

GET https://conductscience.org/api/trials/v1/NCT02147834/registered