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The Impact of Compound Danshen Dropping Pills (CDDP) on the Post-myocardial Infarction Ventricular Remodeling

Primary Purpose

Myocardial Infarction

Status
Recruiting
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Compound Danshen Dropping Pills (CDDP)
Placebo
Sponsored by
The First Affiliated Hospital with Nanjing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myocardial Infarction focused on measuring Myocardial Infarction, Ventricular Remodeling, CDDP

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Aged 18-75 years, gender unlimited;
  2. According to the guidelines for diagnosis and treatment of acute ST segment elevation myocardial infarction (2019), patients with acute anterior ST segment elevation myocardial infarction were diagnosed;
  3. Patients with primary acute myocardial infarction;
  4. Patients who completed PCI reperfusion treatment within 12 hours after the onset of the disease;
  5. Subjects participated in the study voluntarily and signed informed consent.

Exclusion Criteria:

  1. Patients with previous cardiac insufficiency caused by other diseases (valvular heart disease, congenital heart disease, pericardial disease, arrhythmia, other non cardiac causes);
  2. The patients underwent coronary artery bypass graft(CABG) within 12 weeks;
  3. Patients undergoing cardiac resynchronization;
  4. Patients with left ventricular outflow tract obstruction;
  5. Patients with myocarditis;
  6. Patients with uncontrolled severe arrhythmia;
  7. Patients with aortic aneurysm;
  8. Patients with serious liver, kidney, blood system, mental disease or systemic disease;
  9. Significant liver and kidney dysfunction (ALT > 2.0 times the upper limit of normal value; creatinine > 1.5 times the upper limit of normal value);
  10. Patients with serum potassium > 5.5mmol/l;
  11. Uncontrolled hypertension (higher than 180 / 110mmhg);
  12. Pregnant or lactating women;
  13. Patients allergic to compound Danshen Dropping Pills; 1
  14. Patients participating in clinical studies of other drugs.

Sites / Locations

  • First Affiliated Hospital of Nanjing Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Experimental group

Control group

Arm Description

Outcomes

Primary Outcome Measures

ultrasonic cardiogram:left ventricle ejection fraction (LVEF)
LVEF refers to the percentage of stroke output to left ventricular end-diastolic volume and it can be examined by ultrasonic cardiogram.
ultrasonic cardiogram:left ventricular end-diastolic volume index (LVEDVI)
LVEDVI(ml/m2)=left ventricular end-diastolic volume(ml)/body surface area(m2). It can be examined by ultrasonic cardiogram.
ultrasonic cardiogram:left ventricular end-systolic volume index (LVESVI)
LVESVI(ml/m2)=left ventricular end-systolic volume(ml)/body surface area(m2). It can be examined by ultrasonic cardiogram.

Secondary Outcome Measures

N terminal pro-B-type natriuretic peptide(NT-proBNP )decline level
N terminal pro-B-type natriuretic peptide(NT-proBNP )is obtained by blood test.
Adverse cardiovascular events

Full Information

First Posted
August 2, 2021
Last Updated
April 10, 2023
Sponsor
The First Affiliated Hospital with Nanjing Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT05000411
Brief Title
The Impact of Compound Danshen Dropping Pills (CDDP) on the Post-myocardial Infarction Ventricular Remodeling
Official Title
The Impact of Traditional Chinese Medicine, Compound Danshen Dropping Pills (CDDP) on the Post-myocardial Infarction Ventricular Remodeling: A Multicentre, Randomized, Double-blind, Placebo-controlled, Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 25, 2021 (Actual)
Primary Completion Date
August 25, 2023 (Anticipated)
Study Completion Date
March 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First Affiliated Hospital with Nanjing Medical University

4. Oversight

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

5. Study Description

Brief Summary
This study is designed to evaluate the efficacy and safety of compound Danshen dropping pills (CDDP) in improving ventricular remodeling and cardiac function after acute anterior wall ST-Elevation myocardial infarction(STEMI). 268 patients with acute anterior wall STEMI after primary Percutaneous Coronary Intervention (pPCI) are randomly assigned 1:1 to CDDP group(n=134) and control group(n=134) with follow-up of 24 weeks. Both groups are treated with standard therapy of STEMI, with the CDDP group administrating 20 tablets of CDDP before pPCI and 10 tablets three times a day after pPCI and the control group treated with placebo at the same time. The primary endpoint is 24-week echocardiographic including left ventricle ejection fraction (LVEF) , left ventricular end-diastolic volume index (LVEDVI) and left ventricular end-systolic volume index (LVESVI).The secondary endpoint is the change in N terminal pro-B-type natriuretic peptide(NT-proBNP )level, arrhythmia and cardiovascular events (death, cardiac arrest or cardiopulmonary resuscitation, hospitalization due to heart failure or angina pectoris).
Detailed Description
Background: Progressive ventricular remodeling after acute anterior wall myocardial infarction(MI)is an important factor in the occurrence and death of heart failure. Angiotensin converting enzyme inhibitors and beta-blockers can ameliorate post-MI ventricular remodeling, but high-dose therapy can't be tolerable because of hemodynamic instability in the early stage of acute mycardial infarction(AMI). It is known that traditional Chinese medicine, compound Danshen dropping pills (CDDP) exerts protective effect on microcirculatory disturbance caused by ischemia-reperfusion injury and improves energy metabolism after acute myocardial ischemia. Experimental studies have shown CDDP may attenuate ventricular remodeling after myocardial infarction. Methods:This study is designed to evaluate the efficacy and safety of CDDP in improving ventricular remodeling and cardiac function after acute anterior wall ST-Elevation MI(STEMI). 268 patients with acute anterior wall STEMI after primary Percutaneous Coronary Intervention (pPCI) are randomly assigned 1:1 to CDDP group(n=134) and control group(n=134) with follow-up of 24 weeks. Both groups are treated with standard therapy of STEMI, with the CDDP group administrating 20 tablets of CDDP before pPCI and 10 tablets three times a day after pPCI and the control group treated with placebo at the same time. The primary endpoint is 24-week echocardiographic including left ventricle ejection fraction (LVEF) , left ventricular end-diastolic volume index (LVEDVI) and left ventricular end-systolic volume index (LVESVI).The secondary endpoint is the change in N terminal pro-B-type natriuretic peptide(NT-proBNP) level, arrhythmia and cardiovascular events (death, cardiac arrest or cardiopulmonary resuscitation, hospitalization due to heart failure or angina pectoris). Discussion:This is the first prospective study that will demonstrate the impact of CDDP on ventricular remodeling and cardiac function in patients treated with pPCI for a first acute anterior wall STEMI .This study may provide novel insights of Traditional Chinese Medicine , CDDP to improve ventricular remodeling.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction
Keywords
Myocardial Infarction, Ventricular Remodeling, CDDP

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
268 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Title
Control group
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Compound Danshen Dropping Pills (CDDP)
Intervention Description
The patients in this group are treated with 20 tablets of Compound Danshen Dropping Pills (CDDP) before primary Percutaneous Coronary Intervention (pPCI) and 10 tablets three times a day after pPCI.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
The patients in this group take 20 tablets of placebo before primary Percutaneous Coronary Intervention (pPCI) and 10 tablets three times a day after pPCI .
Primary Outcome Measure Information:
Title
ultrasonic cardiogram:left ventricle ejection fraction (LVEF)
Description
LVEF refers to the percentage of stroke output to left ventricular end-diastolic volume and it can be examined by ultrasonic cardiogram.
Time Frame
Week 24
Title
ultrasonic cardiogram:left ventricular end-diastolic volume index (LVEDVI)
Description
LVEDVI(ml/m2)=left ventricular end-diastolic volume(ml)/body surface area(m2). It can be examined by ultrasonic cardiogram.
Time Frame
Week 24
Title
ultrasonic cardiogram:left ventricular end-systolic volume index (LVESVI)
Description
LVESVI(ml/m2)=left ventricular end-systolic volume(ml)/body surface area(m2). It can be examined by ultrasonic cardiogram.
Time Frame
Week 24
Secondary Outcome Measure Information:
Title
N terminal pro-B-type natriuretic peptide(NT-proBNP )decline level
Description
N terminal pro-B-type natriuretic peptide(NT-proBNP )is obtained by blood test.
Time Frame
Day 0/ Day 3/ Day 7/ Week 4/ Week 24/ Week 48
Title
Adverse cardiovascular events
Time Frame
Day 0 to Week 48

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18-75 years, gender unlimited; According to the guidelines for diagnosis and treatment of acute ST segment elevation myocardial infarction (2019), patients with acute anterior ST segment elevation myocardial infarction were diagnosed; Patients with primary acute myocardial infarction; Patients who completed PCI reperfusion treatment within 12 hours after the onset of the disease; Patients categorized as Classes I, II or III according to Killip classification on admission; Subjects participated in the study voluntarily and signed informed consent. Exclusion Criteria: Patients with previous cardiac insufficiency caused by other diseases (valvular heart disease, congenital heart disease, pericardial disease, arrhythmia, other non cardiac causes); The patients underwent coronary artery bypass graft(CABG) within 12 weeks; Patients undergoing cardiac resynchronization; Patients with left ventricular outflow tract obstruction; Patients with myocarditis; Patients with uncontrolled severe arrhythmia; Patients with aortic aneurysm; Patients with serious liver, kidney, blood system, mental disease or systemic disease; Significant liver and kidney dysfunction (ALT > 2.0 times the upper limit of normal value; creatinine > 1.5 times the upper limit of normal value); Patients with serum potassium > 5.5mmol/l; Uncontrolled hypertension (higher than 180 / 110mmhg); Pregnant or lactating women; Patients allergic to compound Danshen Dropping Pills; 1 Patients participating in clinical studies of other drugs.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liansheng Wang
Phone
+86 13390787111
Email
drlswang@njmu.edu.cn
Facility Information:
Facility Name
First Affiliated Hospital of Nanjing Medical University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liansheng Wang, Doctor
Phone
025 68303125
Email
drlswang@njmu.edu.cn

12. IPD Sharing Statement

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The Impact of Compound Danshen Dropping Pills (CDDP) on the Post-myocardial Infarction Ventricular Remodeling

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