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Pharmacogenetics study of hydrochlorothiazide and felodipine in Chinese hypertensive patients

Pharmacogenetics study of hydrochlorothiazide and felodipine in Chinese hypertensive patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCH-12002710
Enrollment
Unknown
Registered
2012-11-21
Start date
1995-01-10
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hypertension

Interventions

Hydrochlorothiazide:Hydrochlorothiazide
Hydrochlorothiazide+Felodipine:Hydrochlorothiazide+Felodipine

Sponsors

Institute of Clinical Pharmacology, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) Patients diagnosed with primary hypertension; (2) aged between 50 and 79.

Exclusion criteria

Exclusion criteria: Secondary hypertension; pregnant or lactating were excluded from this study

Design outcomes

Primary

MeasureTime frame
related gene;Blood pressure;

Countries

China

Contacts

Public ContactWei Zhang
yjsd2003@163.com+86 0731 84805380

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026