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Study of Herbal Formula Corresponding to Syndrome in Treating Post Percutaneous Coronary Intervention (PCI) Patients With Coronary Heart Disease (CHD)

Primary Purpose

Coronary Heart Disease

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Xuefu Zhuyu Capsules Plus Placebo of Sheng Mai Capsules,
Sheng Mai Capsules Plus Placebo of Xuefu Zhuyu Capsules
Placebo of Xuefu Zhuyu Capsules Plus Placebo of Sheng Mai Capsules
Sponsored by
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Heart Disease focused on measuring Coronary Heart Disease, PCI, Traditional Chinese Medicine, Quality of Life

Eligibility Criteria

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

Inclusion Criteria:

  • 18-75 years old
  • Clinical diagnosis of coronary heart disease (confirmed by coronary angiography)
  • Successfully received interventional therapy (PTCA or PCI)
  • belong to TCM blood-stasis syndrome
  • Must be able to swallow tablets
  • Able to give written informed consent

Exclusion Criteria:

  • Symptomatic congestive heart failure(New York Heart Association class III-IV)
  • Females during pregnancy or lactation
  • Serious dysfunction in important organs (liver, lung, kidney,et al)
  • Use of concomitant Chinese herbal medicine
  • Already attend other clinical trial

Sites / Locations

  • Guang'an Men Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Xuefu Zhuyu Capsules

Sheng Mai Capsules

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Severity of anginal attacks, alternations of TCM symptoms and signs, and electrocardiographic changes.

Secondary Outcome Measures

Health related quality of life (Hr-QoL); Changes in serum lipid, inflammatory reaction level and endothelial function status alternations before and after the treatment.

Full Information

First Posted
January 4, 2009
Last Updated
May 31, 2012
Sponsor
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Collaborators
Beijing Anzhen Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00817024
Brief Title
Study of Herbal Formula Corresponding to Syndrome in Treating Post Percutaneous Coronary Intervention (PCI) Patients With Coronary Heart Disease (CHD)
Official Title
Clinical Study of Herbal Formula in Post PCI Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
March 2008 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
March 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Collaborators
Beijing Anzhen Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
We conduct this clinical trial to determine the effects of Xuefu Zhuyu capsule (based on TCM "Zheng Hou" theory) in helping recovery from coronary heart disease(CHD)after PCI and find out whether this kind of effecacy is much better within patients administered with TCM syndrome-based individualized medication.
Detailed Description
The effectiveness of a Chinese herbal formulae is not completely based on the disease or some biomedical indexes, but much more on the TCM syndrome(Chinese name:Zheng Hou)which is generalized from patients' TCM signs and symptoms. Thus, conventional medical curative effecacy evaluation system seems not to so fit for TCM clinical studies. Although many clinical studies from Chinese literature have reported the beneficial effects of various of TCM herbal agents in improving symptoms and signs as well as antagonism of specific pathological changes in CHD patients, most of these trials are lack of well-designed methodologies and the reliability of results still remains unclear. Therefore, we designed this clinical trial, with a randomized, placebo controlled way, to evaluate the curative effects of Xuefu Zhuyu capsule(a Chinese herbal medicine)in patients with Post-PCI CHD patients and find out whether this effects will be better displayed within subjects administered with syndrome-based individualized medication.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Heart Disease
Keywords
Coronary Heart Disease, PCI, Traditional Chinese Medicine, Quality of Life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Xuefu Zhuyu Capsules
Arm Type
Experimental
Arm Title
Sheng Mai Capsules
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Xuefu Zhuyu Capsules Plus Placebo of Sheng Mai Capsules,
Intervention Description
3# XFZY capsules plus 3# placebo of SM capsules, po, Tid, for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Sheng Mai Capsules Plus Placebo of Xuefu Zhuyu Capsules
Intervention Description
3# SM capsules plus 3# placebo of XFZY capsules, po, Tid, for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo of Xuefu Zhuyu Capsules Plus Placebo of Sheng Mai Capsules
Intervention Description
3# Placebo of XFZY capsules plus 3# placebo of SM capsules, po, Tid, for 4 weeks
Primary Outcome Measure Information:
Title
Severity of anginal attacks, alternations of TCM symptoms and signs, and electrocardiographic changes.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Health related quality of life (Hr-QoL); Changes in serum lipid, inflammatory reaction level and endothelial function status alternations before and after the treatment.
Time Frame
4 weeks

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: 18-75 years old Clinical diagnosis of coronary heart disease (confirmed by coronary angiography) Successfully received interventional therapy (PTCA or PCI) belong to TCM blood-stasis syndrome Must be able to swallow tablets Able to give written informed consent Exclusion Criteria: Symptomatic congestive heart failure(New York Heart Association class III-IV) Females during pregnancy or lactation Serious dysfunction in important organs (liver, lung, kidney,et al) Use of concomitant Chinese herbal medicine Already attend other clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jie Wang, M.D.
Organizational Affiliation
China Academy of Chinese Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guang'an Men Hospital
City
Beijing
ZIP/Postal Code
100053
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
20535581
Citation
Chu FY, Wang J, Yao KW, Li ZZ. Effect of Xuefu Zhuyu Capsule (血府逐瘀胶囊) on the symptoms and signs and health-related quality of life in the unstable angina patients with blood-stasis syndrome after percutaneous coronary intervention: A Randomized controlled trial. Chin J Integr Med. 2010 Oct;16(5):399-405. doi: 10.1007/s11655-010-9999-9. Epub 2010 Jun 10.
Results Reference
derived
PubMed Identifier
19671410
Citation
Chu FY, Wang J, Sun XW, Xing YW, Yao KW, Wang SH, Li ZZ. [A randomized double-blinded controlled trial of Xuefu Zhuyu Capsule on short-term quality of life in unstable anginal patients with blood-stasis syndrome after percutaneous coronary intervention]. Zhong Xi Yi Jie He Xue Bao. 2009 Aug;7(8):729-35. doi: 10.3736/jcim20090805. Chinese.
Results Reference
derived

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Study of Herbal Formula Corresponding to Syndrome in Treating Post Percutaneous Coronary Intervention (PCI) Patients With Coronary Heart Disease (CHD)

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