To Evaluate the Efficacy and Safety of Wenxin Keli in Treating Atrial Premature Beats

Beijing Bozhiyin T&S

Status and phase: Unknown; Phase 4

Conditions: Atrial Premature Beats

Treatments: Drug: High dose WenXin keli; Drug: Low dose WenXin keli

Study type: Interventional

Funder types: Industry

Identifiers

NCT02319603

WX-20141022

Details and patient eligibility

About

A randomized, double-blind, two dose group, parallel-control multi-center, post-marketing clinical trial，to evaluate the efficacy and safety of Wenxin keli in treating atrial premature beats by different dose,to provide a scientific basis for rational clinical use of drug.

Full description

Research purpose： To evaluate the efficacy and safety of Wenxin keli in treating atrial premature beats by different dose,to provide a scientific basis for rational clinical use of drug.

Research design： A randomized, double-blind, two dose group, parallel-control multi-center, post-marketing clinical trial.

Sample size:

A total of 288 subjects, 144cases in each group.

Therapeutic schedule:

1. Low dose group (the original quantity Wenxin keli): specification 10g /bag, Wenxin keli (no sugar) 5 g+ Wenxin keli simulation agent 5g.
2. High dose group(2 times the amount of Wenxin keli): specification 10g /bag, Wenxin keli (no sugar) 10 g.

Usage and Dosage:

Oral ,1bag each time, 3 times a day, 4 weeks for 1 course of treatment.

Drug combination:

During the test shall not merge the other anti-arrhythmic drugs beyond the provisions of this scheme. Due to merger disease or condition changes ,have to use drugs or other treatment, investigators must record the types (or other treatment ),drug usage, time and reasons, in order to summarize ,analyze and report.

Primary indicator:

24 h dynamic electrocardiogram (Holter): before treatment, after treatment of 4 w, each record at a time.

Secondary Indicator:

Symptom scores: before treatment, after treatment of 4 w, each record at a time.

Security index:

1. Vital signs: before treatment, after treatment of 4 w, each record at a time.
2. Blood, urine, stool occult blood ,liver and kidney function, blood coagulation four, electrolyte examination, electrocardiogram(ecg): before treatment, after treatment of 4 w, each record at a time.

Main efficacy:

Holter efficient curative effect (main efficacy index) Effective: premature beat frequency reduced 50% or more before taking the medicine.

Invalid: no effective standard.

Secondary efficacy:

Symptom scores curative effect Effective:symptoms improve symptoms(drop 1or above) Invalid: no effective standard.

Statistic analysis:

Main efficacy index by means of FAS,PPS analysis ,safety index SS set analysis.

Enrollment: 288 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Accord with the diagnostic criteria of arrhythmia (atrial premature beats )
• The average number of premature beat of 24 h dynamic electrocardiogram >360 times/h (effective record at least 22 h)
• Stop using the anti- arrhythmic drugs for more than five half-life (except that who long-term (one month or more) with beta blockers for high blood pressure and exertional angina)
• Ages 18 to 75 years old ,all genders
• Voluntary subjects and signed the informed consent form

Exclusion criteria

• Need to merge other anti-arrhythmic drugs(Ⅰ,Ⅱ,Ⅲ,Ⅳ) for serious condition
• Heart rhythm disorders caused by the factors such as drugs ,electrolyte and acid-base balance disorders
• Merge tardy arrhythmia (including sick sinus syndrome and Ⅱdegree atrioventricular block)
• Patients have had heart percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG) surgery
• Patients with severe hypotension
• With serious cardiovascular diseases (severe coronary heart disease, congenital heart disease, cardiomyopathy, myocardial infarction, congestive heart failure, cardiac shock, etc.), cerebrovascular disease, severe respiratory diseases (chronic obstructive pulmonary disease, pulmonary hypertension, pulmonary embolism, etc.),serious primary diseases such as liver, kidney and hematopoietic system (ALT,AST,BUN 2 times higher than normal ceiling, or Cr higher than the upper limit of normal)
• Allergic constitution; the test drug allergy or its ingredients or elements allergy
• Pregnancy and lactation women ,recent preparation pregnancy
• With chronic alcoholism , drug dependence, mental illness
• Participated in other clinical trials within 3 months
• Patients thought by the investigators not suitable to participate in clinical trials

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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288 participants in 2 patient groups

Low dose WenXin keli

Active Comparator group

Description:

Low dose group (the original quantity Wenxin keli): specification 10g /bag, Wenxin keli (no sugar) 5 g+ Wenxin keli simulation agent 5g. Oral ,1 bag each time, 3 times a day, 4 weeks for 1 course of treatment.

Treatment:

Drug: Low dose WenXin keli

High dose WenXin keli

Experimental group

Description:

High dose group(2 times the amount of Wenxin keli): specification 10g /bag, Wenxin keli (no sugar) 10 g. Oral ,1 bag each time, 3 times a day, 4 weeks for 1 course of treatment.

Treatment:

Drug: High dose WenXin keli