Multi-provincial Cohort for Hypertension (MUCH)

Sponsor
Beijing Institute of Heart, Lung and Blood Vessel Diseases (Other)
Overall Status
Unknown status
CT.gov ID
NCT03150888
Collaborator
Beijing Tsinghua Chang Gung Hospital (Other), Beijing Tiantan Hospital (Other), Ruijin Hospital (Other), Nanfang Hospital of Southern Medical University (Other), Southwest Hospital, China (Other)
30,000
6
41
5000
122

Study Details

Study Description

Brief Summary

The purpose of this study is to construct hypertension specialized cohort using uniform standards and specifications. This study timely collected multi-dimensional clinical information through electronic medical records, mobile health, data integration, informatics and computer modern techniques, linking self-reported data and big data platforms from different sources to timely obtain the incidence and mortality data, and integrating hypertension cohort samples and the associated clinical records systematically, in order to build a 30-thousand hypertension specialized cohort with fine phenotypic data and blood/urine samples, thus far to provide support for the development of precise medicine research and related industries.

Condition or Disease Intervention/Treatment Phase
  • Drug: Antihypertensive Agents
  • Other: Cardiovascular risk factors

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
30000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Multi-provincial Cohort for Hypertension in China
Actual Study Start Date :
Jul 3, 2017
Anticipated Primary Completion Date :
Dec 1, 2020
Anticipated Study Completion Date :
Dec 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Hospital based hypertension cohort

Drug: Antihypertensive Agents
Single or combination therapy with five type of antihypertensive agents, such as Ca channel blockers, ACE inhibitors, ARBs, diuretics, or beta-blockers.

Other: Cardiovascular risk factors
Different level of cardiovascular risk factors associated with genetics, environments and lifestyles.

Community based hypertension cohort

Drug: Antihypertensive Agents
Single or combination therapy with five type of antihypertensive agents, such as Ca channel blockers, ACE inhibitors, ARBs, diuretics, or beta-blockers.

Other: Cardiovascular risk factors
Different level of cardiovascular risk factors associated with genetics, environments and lifestyles.

Outcome Measures

Primary Outcome Measures

  1. Composite end point of major cardiovascular and cerebrovascular events [From date of enrollment until date of first documented event or date of death from cardiovascular and cerebrovascular events, whichever came first, assessed up to 3 year]

    Composite end point of major cardiovascular and cerebrovascular events

Secondary Outcome Measures

  1. New-onset of cardiovascular events [From date of enrollment until date of first documented event or date of death from cardiovascular and cerebrovascular events, whichever came first, assessed up to 3 year]

    New-onset of cardiovascular events

  2. New-onset of stroke [From date of enrollment until date of first documented event or date of death from cardiovascular and cerebrovascular events, whichever came first, assessed up to 3 year]

    New-onset of stroke

  3. Total death [From date of enrollment until date of death from all cause, assessed up to 3 year]

    Total death

  4. Major bleeding [From date of enrollment until date of first documented event or date of death from cardiovascular and cerebrovascular events, whichever came first, assessed up to 3 year]

    Major bleeding

  5. Atrial fibrillation [From date of enrollment until date of first documented event or date of death from cardiovascular and cerebrovascular events, whichever came first, assessed up to 3 year]

    Atrial fibrillation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis of hypertension

  • over 18 years old

  • ti sign the informed consent

Exclusion Criteria:
  • with life-threatening severe disease, such as severe tumor or AIDs

  • pregnancy or lactating women,or plan to pregnant within half a year,

  • with severe mental disorders

  • participating in clinical trials

Contacts and Locations

Locations

Site City State Country Postal Code
1 Beijing Anzhen Hospital Beijing China
2 Beijing Tiantan Hospital Beijing China
3 Beijing Tsinghua Chang Gung Hospital Beijing China
4 Southwest Hospital, China Chongqing China
5 Nanfang Hospital of Southern Medical University Guangzhou China
6 Ruijin Hospital Shanghai China

Sponsors and Collaborators

  • Beijing Institute of Heart, Lung and Blood Vessel Diseases
  • Beijing Tsinghua Chang Gung Hospital
  • Beijing Tiantan Hospital
  • Ruijin Hospital
  • Nanfang Hospital of Southern Medical University
  • Southwest Hospital, China

Investigators

  • Principal Investigator: Jing Liu, MD,PhD, Beijing Institute of Heart, Lung and Blood Vessel Diseases

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Beijing Institute of Heart, Lung and Blood Vessel Diseases
ClinicalTrials.gov Identifier:
NCT03150888
Other Study ID Numbers:
  • 2016YFC0900902
First Posted:
May 12, 2017
Last Update Posted:
Jan 22, 2020
Last Verified:
Jan 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 22, 2020