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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04161001
Other study ID # DW_DWJ1451301
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date November 20, 2019
Est. completion date February 2, 2022

Study information

Verified date November 2019
Source Daewoong Pharmaceutical Co. LTD.
Contact Daewoong clinical
Phone +82-2-550-8800
Email shj@daewoong.co.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

- the change of sitSBP based on baseline between Treatment arm and control 1 arm [ Time Frame: 8 weeks ]

- the change of LDL-C based on baseline between Treatment arm and control2 arm [ Time Frame: 8 weeks ]


Recruitment information / eligibility

Status Recruiting
Enrollment 237
Est. completion date February 2, 2022
Est. primary completion date November 20, 2021
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria:

- Age 19 to 80 years

- patients with hypertension and hyperlipidemias

Exclusion Criteria:

- orthostatic hypotension

- History of ventricular tachycardia, atrial fibrillation

- uncontrolled diabetes mellitus

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Amlodipine/Olmesartan 10/40mg (Combination drug), Ezetimibe/Rosuvastatin 10/20mg(Combination drug)
co-administration of Sevikar tab. 10/40mg(Amlodipine/Olmesartan 10/40mg), Rosuzet Tab. 10/20mg(Ezetimibe/Rosuvastatin 10/20mg) and placebo of Olmetec Tab. 40mg(Olmesartan 40mg)
Olmesartan 40mg, Ezetimibe/Rosuvastatin 10/20mg(Combination drug)
co-administration of Olmetec tab. 40mg(Olmesartan 40mg), Rosuzet Tab. 10/20mg(Ezetimibe/Rosuvastatin 10/20mg) and placebo of Sevikar tab. 10/40mg (Amlodipine/Olmesartan 10/40mg)
Amlodipine/Olmesartan 10/40mg (Combination drug)
co-administration of Sevikar tab. 10/40mg(Amlodipine/Olmesartan 10/40mg, and placebo of Rosuzet Tab. 10/20mg(Ezetimibe/Rosuvastatin 10/20mg), Olmetec Tab. 40mg(Olmesartan 40mg)

Locations

Country Name City State
Korea, Republic of Yonsei University Health System, Severance Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Daewoong Pharmaceutical Co. LTD.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary the change of MSSBP based on baseline between Treatment arm and control 1 arm 8 weeks
Primary the change of LDL-C based on baseline between Treatment arm and control2 arm 8 weeks
See also
  Status Clinical Trial Phase
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