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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03012295
Other study ID # HYP-1000
Secondary ID
Status Recruiting
Phase N/A
First received January 3, 2017
Last updated January 4, 2017
Start date August 2016

Study information

Verified date January 2017
Source Chinese Academy of Medical Sciences, Fuwai Hospital
Contact Jun Cai, MD,Ph.D.
Phone +86-010-88322161
Email caijun@fuwaihospital.org
Is FDA regulated No
Health authority China: Chinese Academy of Medical Sciences
Study type Observational

Clinical Trial Summary

Monogenic hypertension, which follows the rules of Mendel's genetic law, is one of the most important causes of hypertension. Generally, patients occur hypertension in early age, have family history, and often manifest severe hypertension or refractory hypertension. At present, only a few hypertension centers of hospitals in China will help clinically difficult diagnosis hypertensive patients to test some selective genes, while most of other hospitals still perform diagnosis based on biochemical examination and clinical symptoms. Therefore, in order to provide better guidance for the diagnosis and treatment for hypertensive patients, this project aims to develop a single gene detection panel for genetic hypertension, so as to provide new diagnostic technology for early intervention, prevention and treatment of hypertension in clinics.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender Both
Age group N/A to 50 Years
Eligibility Inclusion Criteria:

- hypertension patients meet one of the following criteria

1. Beginning age of hypertension: <35 years (regardless of family history of hypertension);

2. refractory hypertension (blood pressure is difficult to control): triple antihypertensive drugs treatment for 1 months, 3 times of non-continuous high blood pressure in consulting room (SBP =140mmHg and/or DBP=90mmHg);

- patients suspected of secondary hypertension, meeting one of the following criteria

1. pheochromocytoma or Cushing syndrome;

2. hypertension with hypokalemia;

3. hypertension with hyperkalemia;

4. hypertension with special body shape, such as central obesity, moon face, acne etc..

5. adrenal tumor;

Exclusion Criteria:

- renal parenchymal / renovascular hypertension

- patients exceed age of 50, and with coronary heart disease and arteriosclerosis

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China CIFuwaiHospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Chinese Academy of Medical Sciences, Fuwai Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of genetic variants in Monogenic Hypertension patients as assessed by specific gene panel one year No