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Early Intervention Study of Nifedipine Controlled Release Tablets on Mild Hypertension Patients with High PWV

Early Intervention Study of Nifedipine Controlled Release Tablets on Mild Hypertension Patients with High PWV

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-13004063
Enrollment
Unknown
Registered
2013-12-30
Start date
2014-01-06
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

1:Nifedipine Controlled Release Tablets

Sponsors

the Second Hosptial of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Female or male aged between 18-75 years; 2. Agreed and signed informed consent; 3. 24-hour ambulatory blood pressure monitoring diagnosed with high blood pressure,(during the daytime> 140/90mmHg, nighttime> 125/75mmHg), except white coat hypertension; 4. Clinic blood pressure levels: 160mmHg > SBP >=140mmHg, or 100 mmHg >DBP >=90mmHg; 5. Ankle-brachial pulse wave velocity >=12m/s.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women;Note:Women of reproductive age are required to attend urine pregnancy test before the first sudy and take contraceptive measures during the test; 2. The patients who participated in other clinical trials in less than three months; 3. The patients who had participated in the study; 4. The patients who not be tolerated with nifedipine or its components; 5. Researchers believe that the patient is not suitable for participating in this study; 6. Moderate to severe hypertension. DBP >=100 mm Hg and/or SBP >=160 mmHg; 7. The patient who are taking any kind of antihypertensive drugs; 8. The patients's concomitant treatment containing a cytochrome P450-3A4 inhibitor or inducer; 9. Secondary hypertension; 10. History of cardiogenic shock; 11. The patient who had myocardial infarction or unstable angina within the past six months; 12. Severe valvular disease; 13. The patients who had or have serious heart rhythm abnormalities or conduction disorders; 14. The patients who had crebral ischemic events within the past 12 months; 15. The patients who have intracranial hemorrhage or subarachnoid hemorrhage in the past 12 months; 16. Type 1 or type 2 diabetes; 17. The patients who have gastrointestinal disorders which may cause malabsorption; 18. The patients who have severe gastrointestinal tract constriction or KOCK vesicle; 19. The patients who have liver disease, or AST / ALT higher than three times; kidney failure, creatinine higher than 2.0mg/dl; urine protein (+); 20. The patient who have malignant disease, psychogenia, alcoholism or drug abuse.

Design outcomes

Primary

MeasureTime frame
PW;

Secondary

MeasureTime frame
SBP/DBP;Heart Rate;

Countries

China

Contacts

Public ContactWei Cui

the Second Hosptial of Hebei Medical University

cuiwei@medmail.com.cn+86 15803210936

Outcome results

None listed

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