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Trimetazidine in Myocardial Injury After Percutaneous Coronary Intervention in Patients With Angina and Diabetes (Trimeta)

Primary Purpose

Diabetes Mellitus, Angina, Unstable

Status
Unknown status
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
trimetazidine
Placebo Oral Tablet
Sponsored by
University of Sao Paulo General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetes Mellitus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult men and women aged> 18 years.
  • Diagnosis of unstable angina with chest pain at least 2 hours after arrival at the emergency unit.
  • Measurement of troponin less than the upper limit of the normality of the method.
  • Indication of cardiac catheterization and need for percutaneous coronary intervention with uniarterial stent within 24 hours of admission.
  • No known allergy to trimetazidine.
  • Prior diagnosis of diabetes mellitus under specific treatment.
  • ClCr> 30 mL / min.
  • Signed consent form.

Exclusion Criteria:

  • Pregnancy.
  • Hemodynamic instability (pulmonary congestion / systolic blood pressure less than 90 mmHg).
  • SCA with ST elevation or troponin elevation.
  • Body mass index greater than 40 kg / m2.
  • Use of oral anticoagulant.
  • Orotracheal intubation.
  • Left ventricular outflow tract obstruction.
  • Allergy to iodinated contrast.
  • Thoracic trauma in the last 30 days.
  • Previous surgical myocardial revascularization.
  • Presence of ventricular arrhythmias.

Sites / Locations

  • Instituto do Coração - HMFMUSPRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

trimetazidine

placebo

Arm Description

The randomization will be done with a list generated by the central pharmacy of the Hospital das Clínicas, Medical School, USP. When the patient is randomized to the trimetazidine pill group, he / she will initiate the medication at 70 mg oral dose (2 tablets of Vastarel ® MR 35 mg single dose) 2 hours before the procedure.

The randomization will be done with a list generated by the central pharmacy of the Hospital das Clínicas, Medical School, USP. When randomized to the placebo oral tablets group, the patient will receive placebo (orally, 2 single dose tablets) also 2 hours prior to PCI.

Outcomes

Primary Outcome Measures

peak values of troponin and CKMB after PCI
comparing groups for peak values of troponin and CKMB after PCI.

Secondary Outcome Measures

peak values of CRP
Comparison between groups for peak values of CRP after PCI.
peak values of creatinine
Comparison between groups for peak values of creatinine after PCI.
peak values of leukogram
Comparison between groups for peak values of leukogram after PCI.
occurrence of sustained ventricular arrhythmia
Combined comparison between the occurrence of sustained ventricular arrhythmia
occurrence of cardiogenic shock,
Combined comparison between the occurrence of cardiogenic shock,
occurrence of cardiorespiratory arrest,
Combined comparison between the occurrence of cardiorespiratory arrest
occurrence of worsening of renal function
Combined comparison between the occurrence of worsening of renal function (increase of 0.5 mg / dL in relation to admission creatinine or 25% above baseline)
occurrence of need for reintervention
Combined comparison between the occurrence of need for reintervention
occurrence of cerebrovascular accident
Combined comparison between the occurrence of cerebrovascular accident
occurrence of death
Combined comparison between the occurrence of death

Full Information

First Posted
October 19, 2018
Last Updated
October 22, 2018
Sponsor
University of Sao Paulo General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03715582
Brief Title
Trimetazidine in Myocardial Injury After Percutaneous Coronary Intervention in Patients With Angina and Diabetes
Acronym
Trimeta
Official Title
PROSPECTIVE ANALYSIS BETWEEN TRIMETAZIDINE Versus PLACEBO IN MYOCARDIAL INJURY AFTER PERCUTANEOUS CORONARY INTERVENTION IN PATIENTS WITH INSTANT ANGINA AND DIABETES MELLITUS
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Unknown status
Study Start Date
October 1, 2018 (Actual)
Primary Completion Date
October 1, 2020 (Anticipated)
Study Completion Date
October 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Sao Paulo General Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Introduction: Recent studies have suggested that trimetazidine may help reduce myocardial damage following percutaneous coronary intervention. However, the evaluation of the potential of this medication in the reduction of myocardial damage in patients with diabetes mellitus and unstable angina, in a prospective and randomized way, has not yet been described. Objective: The aim of this study was to evaluate the efficacy and safety of the use of trimetazidine versus placebo in patients with diabetes mellitus and unstable angina undergoing coronary stent angioplasty. Methodology: For this, a unicentric, randomized, double blind and prospective study will be performed in a comparative manner. Hospital data (test results, medical outcomes, drug dose, complications) of patients will be analyzed for safety and effectiveness. Myocardial damage will be measured by means of ultrasensitive Troponin dosages. Expected results: The use of trimetazidine reduces myocardial damage in patients with diabetes mellitus and unstable angina undergoing coronary stent angioplasty.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Angina, Unstable

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
trimetazidine
Arm Type
Experimental
Arm Description
The randomization will be done with a list generated by the central pharmacy of the Hospital das Clínicas, Medical School, USP. When the patient is randomized to the trimetazidine pill group, he / she will initiate the medication at 70 mg oral dose (2 tablets of Vastarel ® MR 35 mg single dose) 2 hours before the procedure.
Arm Title
placebo
Arm Type
Experimental
Arm Description
The randomization will be done with a list generated by the central pharmacy of the Hospital das Clínicas, Medical School, USP. When randomized to the placebo oral tablets group, the patient will receive placebo (orally, 2 single dose tablets) also 2 hours prior to PCI.
Intervention Type
Drug
Intervention Name(s)
trimetazidine
Intervention Description
Pills of masking drug - trimetazidine
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Other Intervention Name(s)
placebo
Intervention Description
Pills of masking drug - placebo
Primary Outcome Measure Information:
Title
peak values of troponin and CKMB after PCI
Description
comparing groups for peak values of troponin and CKMB after PCI.
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
peak values of CRP
Description
Comparison between groups for peak values of CRP after PCI.
Time Frame
24 hours
Title
peak values of creatinine
Description
Comparison between groups for peak values of creatinine after PCI.
Time Frame
24 hours
Title
peak values of leukogram
Description
Comparison between groups for peak values of leukogram after PCI.
Time Frame
24 hours
Title
occurrence of sustained ventricular arrhythmia
Description
Combined comparison between the occurrence of sustained ventricular arrhythmia
Time Frame
24 hours
Title
occurrence of cardiogenic shock,
Description
Combined comparison between the occurrence of cardiogenic shock,
Time Frame
24 hours
Title
occurrence of cardiorespiratory arrest,
Description
Combined comparison between the occurrence of cardiorespiratory arrest
Time Frame
24 hours
Title
occurrence of worsening of renal function
Description
Combined comparison between the occurrence of worsening of renal function (increase of 0.5 mg / dL in relation to admission creatinine or 25% above baseline)
Time Frame
24 hours
Title
occurrence of need for reintervention
Description
Combined comparison between the occurrence of need for reintervention
Time Frame
24 hours
Title
occurrence of cerebrovascular accident
Description
Combined comparison between the occurrence of cerebrovascular accident
Time Frame
24 hours
Title
occurrence of death
Description
Combined comparison between the occurrence of death
Time Frame
24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult men and women aged> 18 years. Diagnosis of unstable angina with chest pain at least 2 hours after arrival at the emergency unit. Measurement of troponin less than the upper limit of the normality of the method. Indication of cardiac catheterization and need for percutaneous coronary intervention with uniarterial stent within 24 hours of admission. No known allergy to trimetazidine. Prior diagnosis of diabetes mellitus under specific treatment. ClCr> 30 mL / min. Signed consent form. Exclusion Criteria: Pregnancy. Hemodynamic instability (pulmonary congestion / systolic blood pressure less than 90 mmHg). SCA with ST elevation or troponin elevation. Body mass index greater than 40 kg / m2. Use of oral anticoagulant. Orotracheal intubation. Left ventricular outflow tract obstruction. Allergy to iodinated contrast. Thoracic trauma in the last 30 days. Previous surgical myocardial revascularization. Presence of ventricular arrhythmias.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alexandre Soeiro, MD
Phone
+55112661-5299
Email
alexandre.soeiro@bol.com.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mucio Tavares, MD
Organizational Affiliation
Unidade Clínica de Emergência
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto do Coração - HMFMUSP
City
São Paulo
ZIP/Postal Code
05403000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alexandre Soeiro, MD
Phone
5511-2661-5299
Email
alexandre.soeiro@bol.com.br

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Trimetazidine in Myocardial Injury After Percutaneous Coronary Intervention in Patients With Angina and Diabetes

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