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China Stroke Primary Prevention Trial (CSPPT)

Primary Purpose

Primary Hypertension

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Enalapril/folic acid
Enalapril maleate
Sponsored by
Shenzhen Ausa Pharmed Co.,Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Primary Hypertension focused on measuring hypertension, stroke, cardiovascular events, enalapril, folic acid, randomized controlled trial, MTHFR C677T genotype

Eligibility Criteria

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

Inclusion Criteria:

  • BP≥140/90 mmHg in both of the two screening visits or currently under anti-hypertension treatment
  • 45 - 75 years old
  • Successful determination of MTHFR C677T genotype
  • For pre-menopausal women, agreed to use contraceptives during the trial
  • Signed the written informed consent

Exclusion Criteria:

  • Having a history of stroke
  • Having a history of myocardial infarction
  • Having a history of physician diagnosed heart failure
  • Post- coronary revascularization
  • Severe somatic disease such as cancer
  • Secondary hypertension
  • Congenital or acquired organic heart diseases
  • Contraindicated to angiotensin-converting enzyme inhibitor(ACEI)
  • History of ACEI adverse effects
  • Currently long-term use of folic acid or vitamin B12 or vitamin B6
  • Pregnant or child breastfeeding women
  • Severe mental disorders
  • Lab tests indicating abnormal liver or kidney function
  • Unwilling to participate the trial, unwilling to change the current antihypertensive treatment

Sites / Locations

  • Anqing Branch, Anhui Institute of Biomedical Research
  • Lianyungang Center for Advanced Research in Cardiovascular Diseases

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Enalapril/folic acid

Enalapril

Arm Description

A fixed combination drug is given. The dose is fixed in enalapril 10 mg / folic acid 0.8 mg per day.

Enalapril maleate 10 mg per day is given

Outcomes

Primary Outcome Measures

First attack of symptomatic stroke ( ischemic or hemorrhagic)
Patients are followed-up every 3 months. All endpoint outcomes are assessed by the Endpoint Adjudication Committee of the study.

Secondary Outcome Measures

Composite major cardiovascular events
All-cause death
First attack of ischemic stroke and resultant death
First attack of hemorrhagic stroke and resultant death
Myocardial infarction and resultant death

Full Information

First Posted
November 19, 2008
Last Updated
August 11, 2014
Sponsor
Shenzhen Ausa Pharmed Co.,Ltd
Collaborators
Anhui Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT00794885
Brief Title
China Stroke Primary Prevention Trial
Acronym
CSPPT
Official Title
Enalapril Maleate and Folic Acid Tablets for Primary Prevention of Stroke in Patients With Hypertension: a Post-marketing, Double-blind, Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
June 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shenzhen Ausa Pharmed Co.,Ltd
Collaborators
Anhui Medical University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this trial is to confirm that enalapril maleate and folic acid tablets is more effective in preventing stroke among the patients with primary hypertension when compared to enalapril maleate.
Detailed Description
Primary hypertension is the most important risk factor leading to cardiovascular events. Successful management of hypertension is a key to prevent these events. Hyperhomocysteinemia (HHcy) is another independent risk factor, especially for stroke. Our team's prospective nested case-control study of 39165 subjects in China showed that incidence of cardiovascular events (especially stroke) was strongly associated with plasma level of total homocysteine (tHcy). The coexistence of hypertension and HHcy dramatically increased the risk of stroke by 25 to 30 times as compared to the subjects without the two risk factors (Graham et al, 1997). Findings from previous and our studies clearly indicate that simultaneous control of hypertension and HHcy is pivotal in reducing cardiovascular events morbidity and mortality in China. It has been well documented that folic acid is effective in lowering the level of plasma tHcy. While controversial remains on its efficacy on preventing cardiovascular events, a study done by our team: "Efficacy of folic acid supplementation in stroke prevention: a meta-analysis" (Wang et al, 2007) provide coherent evidence that folic acid supplementation can decrease the risk of stroke by 18%, and 25% in populations where folic fortification was not issued, or used for primary prevention. C677T gene polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) is one of the genetic determinators of plasma tHcy level. Observational studies showed that individuals with TT genotype tend to have high plasma tHcy and elevated risk of cardiovascular events (Cronin et al. 2005), and folic acid supplementation led to a remarkable reduction in plasma tHcy. In short, previous studies by others and by our team have provided strong rationale for our proposed trial as detailed below. The hypothesis of the current study is that a combination of antihypertensive drug (e.g., enalapril) with folic acid is not only efficacious, but also is safe and highly cost-effective than antihypertensive (e.g., enalapril) used alone to prevent stroke in hypertensive patients. This trial will enroll 20,000 patients with primary hypertension and with known MTHFR C677T genotype. Subjects will be first stratified by genotypes, and then randomly assigned to treatment groups. The study patients will be instructed to take orally enalapril 10 mg daily or enalapril/folic acid 10mg/0.8mg tablets daily for a maximum of 5 years. The follow-up is given every 3 months. The incidence and time of first-time stroke episode (primary endpoint) or composite cardiovascular events are used as endpoints. They will be compared by treatment groups with and without stratification by C677T gene polymorphisms. The potential interaction between treatment groups and C677T gene polymorphisms on therapeutic efficacy will also be tested. This will be the first and largest trial of this kind in Chinese population. The findings from this trial may have the potential to transform current clinical and public health findings into practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Hypertension
Keywords
hypertension, stroke, cardiovascular events, enalapril, folic acid, randomized controlled trial, MTHFR C677T genotype

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20702 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enalapril/folic acid
Arm Type
Experimental
Arm Description
A fixed combination drug is given. The dose is fixed in enalapril 10 mg / folic acid 0.8 mg per day.
Arm Title
Enalapril
Arm Type
Active Comparator
Arm Description
Enalapril maleate 10 mg per day is given
Intervention Type
Drug
Intervention Name(s)
Enalapril/folic acid
Other Intervention Name(s)
Enalapril Maleate and Folic Acid Tablet
Intervention Description
Enalapril/folic acid, (10mg enalapril/0.8mg folic acid)/tablet, taken orally and once daily for a maximum of 5 years. Combination with other anti-hypertension drugs are allowed.
Intervention Type
Drug
Intervention Name(s)
Enalapril maleate
Other Intervention Name(s)
Lameiya,Yabao Pharmaceutical
Intervention Description
Enalapril, 10mg/tablet, taken orally once daily for a maximum of 5 consecutive years. Combination with other anti-hypertension drugs are allowed.
Primary Outcome Measure Information:
Title
First attack of symptomatic stroke ( ischemic or hemorrhagic)
Description
Patients are followed-up every 3 months. All endpoint outcomes are assessed by the Endpoint Adjudication Committee of the study.
Time Frame
during the trial period
Secondary Outcome Measure Information:
Title
Composite major cardiovascular events
Time Frame
during the trial period
Title
All-cause death
Time Frame
during the trial period
Title
First attack of ischemic stroke and resultant death
Time Frame
during the trial period
Title
First attack of hemorrhagic stroke and resultant death
Time Frame
during the trial period
Title
Myocardial infarction and resultant death
Time Frame
during the trial period
Other Pre-specified Outcome Measures:
Title
Malignant tumors
Time Frame
during the trial period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: BP≥140/90 mmHg in both of the two screening visits or currently under anti-hypertension treatment 45 - 75 years old Successful determination of MTHFR C677T genotype For pre-menopausal women, agreed to use contraceptives during the trial Signed the written informed consent Exclusion Criteria: Having a history of stroke Having a history of myocardial infarction Having a history of physician diagnosed heart failure Post- coronary revascularization Severe somatic disease such as cancer Secondary hypertension Congenital or acquired organic heart diseases Contraindicated to angiotensin-converting enzyme inhibitor(ACEI) History of ACEI adverse effects Currently long-term use of folic acid or vitamin B12 or vitamin B6 Pregnant or child breastfeeding women Severe mental disorders Lab tests indicating abnormal liver or kidney function Unwilling to participate the trial, unwilling to change the current antihypertensive treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yong Huo, M.D.
Organizational Affiliation
The First Hospital, Beijing University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Anqing Branch, Anhui Institute of Biomedical Research
City
Anqing City
State/Province
Anhui
ZIP/Postal Code
246000
Country
China
Facility Name
Lianyungang Center for Advanced Research in Cardiovascular Diseases
City
Lianyungang
State/Province
Jiangsu
ZIP/Postal Code
222003
Country
China

12. IPD Sharing Statement

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China Stroke Primary Prevention Trial

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