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Observational Study to Evaluate the Safety of DILATREND SR Cap. in Korean Patients With Essential Hypertension, Chronic Stable Angina and Congestive Heart Failure

Unknown statusNCT03063697
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The purpose of this study is to Evaluate the Safety of DILATREND SR Cap. in Korean Patients with Essential hypertension, Chronic stable angina and Congestive heart failure for 52 weeks.

Study details

Official title
Prospective, Multi-center, Observational Study to Evaluate the Safety of DILATREND SR Cap. in Korean Patients With Essential Hypertension, Chronic Stable Angina and Congestive Heart Failure
Conditions
Sponsor
Chong Kun Dang Pharmaceutical
Start date
2015-11
Primary completion
2020-12
Sex
All
Age range
from 19 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Age 19 years or older Patients with Essential hypertension, Chronic stable angina and Congestive heart failure 2. Possible to take Dilatrend SR on the label 3. not taking Caverdilol for 6 month from Agreement date 4. Agreement with written informed consent Exclusion Criteria: 1. Pregnancy or lactation 2. Known hypersensitivity to Carvedilol 3. Cardiogenic shock 4. Abnormality of the conduction system as Severe bradycardia(In particular, pulse \<50beats / min), 2nd degree AV block, Complete AV block, Sinus Block, Sick Sinus Syndrome 5. Cor pulmonale 6. IDDM with ketoacidosis, metabolic acidosis 7. has severe heart disease(Heart failure NYHA functional class 4) 8. Respiratory diseases as Asthma, Chronic Obstructive Pulmonary Disease 9. Secondary hypertension 10. Prinzmetal's angina 11. Acute pulmonary embolism 12. Pheochromocytoma 13. Take MAO lnhibitor(except for MAO-B) 14. Hypotension ( SBP 90mmHg or less) 15. Severe hepatic dysfunction 16. Peripheral circulatory disturbance( ex. Raynaud syndrome, intermittent claudication) 17. Has edema glottitis 18. Has heart attack with complication 19. Fluid retention or overload to required intravenous inotropes 20. Allergic rhinitis

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03063697