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Efficacy and Safety Study of Guanxin Shutong Capsule to Treat Chronic Stable Angina

Primary Purpose

Angina, Stable

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Guanxin Shutong Capsule
Placebo Capsule
nitroglycerine
Sponsored by
Shaanxi Buchang Pharmaceutical Co., Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Angina, Stable focused on measuring Angina

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Symptom of chronic stable angina is sustained for 3 months or over 3 months (typical symptoms of myocardial ischemia occurred at least 2 times in the latest week, and angina type is stable angina (Canada CCS class Ⅰ、Ⅱ or Ⅲ);
  • Blood stasis resistance on traditional Chinese medicine syndrome differentiation;
  • Patients who meet the following any situation:

    1. had coronary angiography and verified a least one main branch of coronary stenosis ≥50%;
    2. have typical angina symptom, and also have positive ETT result or CTA shows at least one main branch of coronary stenosis ≥50%;
    3. had history of myocardial infarct (at least 6 months).
  • Written informed consent.

Exclusion Criteria:

  • Acute coronary syndrome or highly suspected acute coronary syndrome;
  • Variant angina or unstable angina;
  • Myocardial infarction within the past 6 months;
  • Left main disease and without revascularization was verified through angiography or CTA;
  • Moderate to severe aortic stenosis, hypertrophic Obstructive Cardiomyopathy or congestive heart-failure (NYHA class Ⅲ-Ⅳ);
  • Patients who were received PCI/CABG within 1 year;
  • Patients who are poor control of high blood pressure (SBP>170mmHg, or DBP>100mmHg);
  • Patients who have hypotension (SBP<90mmHg, DBP<60mmHg) or had orthostatic hypotension;
  • ECG shows complete left bundle branch block, pre-excitation syndrome, left ventricular hypertrophy or pacemaker rhythm;
  • Hypohepatia (ALT or bilirubin level is higher than upper limit), renal insufficiency (serum creatinine level is higher than upper limit);
  • Active peptic ulcer or skin ulcer;
  • Diagnosed chest pain caused by severe neurosis, menopausal syndrome, hyperthyroidism, cervical spondylosis, gallbladder-cardiac syndrome, gastroesophageal reflux, esophageal hiatus hernia or in aortic dissection;
  • Patients had hematological disorder, specific bleeding or warfarin caused bleeding;
  • Drug abuser, patients with history of alcoholism in the past 2 years or dependency to known drugs;
  • Psychopath;
  • Patients who can't compelet exercise test (note: just for partial patients who need to complete exercise test);
  • Pregnancy or lactation;
  • Patients who are known or suspected hypersensitive to the study medicine or allergic constitution;
  • Patients who were received big surgery within 4 weeks or participated in other clinical trials within 3 months.

Sites / Locations

  • The General Hospital of Shenyang Military Region

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Guanxin Shutong Capsule

Placebo Capsule

Arm Description

3 capsules once, tid, Oral Duration: 4 weeks

Placebo capsule and Guanxin Shutong Capsule the same appearance are made by SHAANXI BUCHANG PHARMACEUTICAL CO.,LTD. 3 capsules once, tid, Oral Duration: 4 weeks

Outcomes

Primary Outcome Measures

Therapeutic effect to Angina ( Average value of angina frequency)
Record angina frequency per week. Record date is Start-up Stage 1st week, Start-up Stage 2st week, Interview Stage 1st week, Interview Stage 2st week, Interview Stage 3st week and Interview Stage 4st week (Toal of 6 times).
Exercise treadmill testing (ETT)
ST-segment displacement in electrocardiogram: Observe ST-segment displacement of J point after 60ms, including the degree of ST-segment depression.

Secondary Outcome Measures

Usage of nitroglycerine per day (average value)
Seattle Angina Ques-tionnaire (SAQ)
Scores on Chinese medical syndrome scale
Primary symptom: Chest pains (0; Slight: 2; Moderate: 4; Severe: 6) Chest congestion (0; Slight: 2; Moderate: 4; Severe: 6) Secondary symptom: Palpitation (0; Slight: 1; Moderate: 2; Severe: 3) Shortness of breath (0; Slight: 1; Moderate: 2; Severe: 3) Insomnia (0; Slight: 1; Moderate: 2; Severe: 3)
Electrocardiogram manifestation
Compare the changes of electrocardiogram manifestation (such as ST segment, T wave) of angina before and after treatment.
Time of angina break out from exercise beginning in ETT
Time of ST below 1 mm from exercise beginning in ETT

Full Information

First Posted
October 23, 2014
Last Updated
October 29, 2014
Sponsor
Shaanxi Buchang Pharmaceutical Co., Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT02280850
Brief Title
Efficacy and Safety Study of Guanxin Shutong Capsule to Treat Chronic Stable Angina
Official Title
Efficacy and Safety Study of Guanxin Shutong Capsule to Treat Chronic Stable Angina: A Randomised, Double-blind, Placebo-controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2014 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
October 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shaanxi Buchang Pharmaceutical Co., Ltd

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Compared with placebo, assess of the efficacy and safety of Guanxin Shutong capsule to treat chronic stable angina (syndrome of blood stasis resistance), and the result will be used for the basis of later Ⅳ clinical trial.
Detailed Description
1. Procedures 1.1 Start-up stage (-14~0 Day) Inquire medical history, medication use, accompanied treatment, etc; Sign informed consent; Measure vital signs and conduct physical examination; Record symptom and signs; Confirm inclusion/exclusion criteria, and put patients who meet inclusion criteria into start-up stage; Record participators' history of angina pectoris and treatment, or select stable angina from outpatient service (without medicate); Allocate screen number, hand out Guanxi Shutong Capsules Placebo and record card of angina/nitroglycerin used; Advise patient return visit with an empty belly 2 weeks later. 1.2 Interview 1 (Baseline 0 Day) (1) Measure vital signs; (2)Accomplish all the examination items: Blood routines, Urine routines, Stool routines + Occult blood, Hepatorenal function (AST, ALT, TBIL, ALP, γ-GT, BUN, Cr), Four coagulation tests (TT, PT, APTT, FIB), Blood fat (TC, TG, HDL-C, LDL-C), 12 leads electrocardiogram, Seattle Angina Ques-tionnaire (SAQ). Additionally, premenopausal women receive urine pregnancy test; (3) Exercise treadmill testing (ETT): around am. 10:00 (Note: Just for the patients who need ETT); (4) Record symptoms and signs ( Score of syndrome of Chinese medicine and Score of angina); (5) Randomize and allocate drug number; (6) Hand out the drugs for 2 weeks and record card of angina/nitroglycerin used; (7) Advise patient return visit 2 weeks later. 1.3 Interview 2 (14±2 Day) Inquire adverse events; Inquire accompanied treatment and record combined medication. Measure vital signs; Record symptoms and signs (Score of syndrome of Chinese medicine and Score of angina); Withdraw remained drugs and box, and record card; Hand out the drugs for 2 weeks and record card of angina/nitroglycerin used; Advise patient return visit 2 weeks later. 1.4 Interview 3 (28±2 Day) (1) Inquire adverse events; (2) Inquire accompanied treatment and record combined medication. (3) Measure vital signs; (4) Record symptoms and signs (Score of syndrome of Chinese medicine and Score of angina); (5) 12 leads electrocardiogram (6) Accomplish all the examination items: Blood routines, Urine routines, Stool routines + Occult blood, Hepatorenal function (AST, ALT, TBIL, ALP, γ-GT, BUN, Cr), Four coagulation tests (TT, PT, APTT, FIB), Blood fat (TC, TG, HDL-C, LDL-C), 12 leads electrocardiogram, Seattle Angina Ques-tionnaire (SAQ); (7) Exercise treadmill testing (ETT) (Note: Just for the patients who need ETT); (8) Withdraw remained drugs and box, and record card; (9) Assess compliance; (10) Summarize the clinical trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Angina, Stable
Keywords
Angina

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Guanxin Shutong Capsule
Arm Type
Experimental
Arm Description
3 capsules once, tid, Oral Duration: 4 weeks
Arm Title
Placebo Capsule
Arm Type
Placebo Comparator
Arm Description
Placebo capsule and Guanxin Shutong Capsule the same appearance are made by SHAANXI BUCHANG PHARMACEUTICAL CO.,LTD. 3 capsules once, tid, Oral Duration: 4 weeks
Intervention Type
Drug
Intervention Name(s)
Guanxin Shutong Capsule
Intervention Description
3 capsules three times a day; Duration: 4 weeks. Number of Cycles: until progression or unacceptable toxicity develops.
Intervention Type
Drug
Intervention Name(s)
Placebo Capsule
Intervention Description
3 capsules three times a day; Duration: 4 weeks.
Intervention Type
Drug
Intervention Name(s)
nitroglycerine
Intervention Description
Adults: 0.25mg-0.5mg (half pill or 1 pill) once, sub-lingual. One more pill per 5 minutes untill pain relief. If total dose is 3 pills in 15 minutes and the pain is still in, please seek medical advice urgently. The participators in both arms who have agina symptom will take Nitroglycerine. So the accumulated consumption of participators is the one of the maesuremnts.
Primary Outcome Measure Information:
Title
Therapeutic effect to Angina ( Average value of angina frequency)
Description
Record angina frequency per week. Record date is Start-up Stage 1st week, Start-up Stage 2st week, Interview Stage 1st week, Interview Stage 2st week, Interview Stage 3st week and Interview Stage 4st week (Toal of 6 times).
Time Frame
6 weeks
Title
Exercise treadmill testing (ETT)
Description
ST-segment displacement in electrocardiogram: Observe ST-segment displacement of J point after 60ms, including the degree of ST-segment depression.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Usage of nitroglycerine per day (average value)
Time Frame
4 weeks
Title
Seattle Angina Ques-tionnaire (SAQ)
Time Frame
4 weeks
Title
Scores on Chinese medical syndrome scale
Description
Primary symptom: Chest pains (0; Slight: 2; Moderate: 4; Severe: 6) Chest congestion (0; Slight: 2; Moderate: 4; Severe: 6) Secondary symptom: Palpitation (0; Slight: 1; Moderate: 2; Severe: 3) Shortness of breath (0; Slight: 1; Moderate: 2; Severe: 3) Insomnia (0; Slight: 1; Moderate: 2; Severe: 3)
Time Frame
4 weeks
Title
Electrocardiogram manifestation
Description
Compare the changes of electrocardiogram manifestation (such as ST segment, T wave) of angina before and after treatment.
Time Frame
4 weeks
Title
Time of angina break out from exercise beginning in ETT
Time Frame
4 weeks
Title
Time of ST below 1 mm from exercise beginning in ETT
Time Frame
4 weeks
Other Pre-specified Outcome Measures:
Title
Blood fat (TC, TG, HDL-C, LDL-C)
Time Frame
4 weeks
Title
Degree and duration of angina attack.
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptom of chronic stable angina is sustained for 3 months or over 3 months (typical symptoms of myocardial ischemia occurred at least 2 times in the latest week, and angina type is stable angina (Canada CCS class Ⅰ、Ⅱ or Ⅲ); Blood stasis resistance on traditional Chinese medicine syndrome differentiation; Patients who meet the following any situation: had coronary angiography and verified a least one main branch of coronary stenosis ≥50%; have typical angina symptom, and also have positive ETT result or CTA shows at least one main branch of coronary stenosis ≥50%; had history of myocardial infarct (at least 6 months). Written informed consent. Exclusion Criteria: Acute coronary syndrome or highly suspected acute coronary syndrome; Variant angina or unstable angina; Myocardial infarction within the past 6 months; Left main disease and without revascularization was verified through angiography or CTA; Moderate to severe aortic stenosis, hypertrophic Obstructive Cardiomyopathy or congestive heart-failure (NYHA class Ⅲ-Ⅳ); Patients who were received PCI/CABG within 1 year; Patients who are poor control of high blood pressure (SBP>170mmHg, or DBP>100mmHg); Patients who have hypotension (SBP<90mmHg, DBP<60mmHg) or had orthostatic hypotension; ECG shows complete left bundle branch block, pre-excitation syndrome, left ventricular hypertrophy or pacemaker rhythm; Hypohepatia (ALT or bilirubin level is higher than upper limit), renal insufficiency (serum creatinine level is higher than upper limit); Active peptic ulcer or skin ulcer; Diagnosed chest pain caused by severe neurosis, menopausal syndrome, hyperthyroidism, cervical spondylosis, gallbladder-cardiac syndrome, gastroesophageal reflux, esophageal hiatus hernia or in aortic dissection; Patients had hematological disorder, specific bleeding or warfarin caused bleeding; Drug abuser, patients with history of alcoholism in the past 2 years or dependency to known drugs; Psychopath; Patients who can't compelet exercise test (note: just for partial patients who need to complete exercise test); Pregnancy or lactation; Patients who are known or suspected hypersensitive to the study medicine or allergic constitution; Patients who were received big surgery within 4 weeks or participated in other clinical trials within 3 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Han Yaling, Academician
Phone
+86-24-28856123
Email
guanxinshutong@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lv Shuzheng
Organizational Affiliation
Beijing Anzhen Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Zhang Yan
Organizational Affiliation
The Affiliated Hospital of Liaoning Hospital of Traditional Chinese Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chen Bojun
Organizational Affiliation
The Second Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Luo Wei
Organizational Affiliation
Xuzhou Central Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jiang Binghua
Organizational Affiliation
The Second Affiliated Hospital of Shandong University of traditional Chinese Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Zhang Zhenxian
Organizational Affiliation
Luohe Hospital of Traditional Chinese Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xing Yanjun
Organizational Affiliation
First Hospital of Shijiazhuang City
Official's Role
Principal Investigator
Facility Information:
Facility Name
The General Hospital of Shenyang Military Region
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110045
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Han Yaling, Academician
Phone
+86-24-28856123
Email
guanxinshutong@126.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
31829173
Citation
Li Y, Zhang L, Lv S, Wang X, Zhang J, Tian X, Zhang Y, Chen B, Liu D, Yang J, Dong P, Xu Y, Song Y, Shi J, Li L, Wang X, Han Y. Efficacy and safety of oral Guanxinshutong capsules in patients with stable angina pectoris in China: a prospective, multicenter, double-blind, placebo-controlled, randomized clinical trial. BMC Complement Altern Med. 2019 Dec 11;19(1):363. doi: 10.1186/s12906-019-2778-z.
Results Reference
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Efficacy and Safety Study of Guanxin Shutong Capsule to Treat Chronic Stable Angina

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