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Genetic Testing of Monogenic Hypertension in Chinese Population

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03012295
Enrollment
1000
Registered
2017-01-06
Start date
2016-08-31
Completion date
Unknown
Last updated
2017-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Monogenic Hypertension

Keywords

Genetic Testing, Chinese Population

Brief 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.

Interventions

None listed

Sponsors

Chinese Academy of Medical Sciences, Fuwai Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
number of genetic variants in Monogenic Hypertension patients as assessed by specific gene panelone year

Countries

China

Contacts

Primary ContactJun Cai, MD,Ph.D.
caijun@fuwaihospital.org+86-010-88322161

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026