Hypertension, Dyslipidemia Clinical Trial
Official title:
A Multi-center, Randomized, Double-Blind, Phase III Clinical Trial to Evaluate the Efficacy and Safety of DWJ1451 in Patients With Hypertension and Dyslipidemia
- 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 ]
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 |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Yonsei University Health System, Severance Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Daewoong Pharmaceutical Co. LTD. |
Korea, Republic of,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT03648801 -
A Post-marketing Surveillance to Assess Safety and Efficacy of Telostop Plus Tab.
|