An Observation Study on the Identification of Prescription Patterns of Lodient Tab(Telmisartan/S-amlodipine)
1 other identifier
observational
4,000
1 country
1
Brief Summary
This study identify prescription patterns of Lodient Tab and evaluate the changes of the hypertension symptoms (BP pressure) who are first prescribed and taking Lodient Tab.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2021
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 11, 2021
CompletedFirst Submitted
Initial submission to the registry
January 3, 2024
CompletedFirst Posted
Study publicly available on registry
January 22, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2025
CompletedJanuary 22, 2024
January 1, 2024
3.1 years
January 3, 2024
January 17, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
The percentage of patients who met target systolic blood pressure (less than 140mmHg) at 6 months of prescription for Lodient Tab compared to baseline
The percentage of patients who met target systolic blood pressure (less than 140mmHg) at 6 months of prescription for Lodient Tab compared to baseline
at 6 months of prescription for Lodient Tab compared to baseline
Eligibility Criteria
Patients Prescribed Lodient Tab for Hypertension Treatment
You may qualify if:
- Adults over 19 years of age
- A person diagnosed with hypertension
- A person who has been first prescribed Lodient Tab within the past 4 months as of the IRB approval date or is scheduled to be prescribed Lodient Tab
- A person who voluntarily agreed in writing to this study
You may not qualify if:
- Pregnant women or nursing mothers
- Persons subject to prohibition according to the permission of the Lodient Tab
- Patients who in the judgement of the investigator, were inappropriate to participate in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Seoul song clinic
Seoul, South Korea
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Minseob Song
Seoul song clinic
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Months
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 3, 2024
First Posted
January 22, 2024
Study Start
November 11, 2021
Primary Completion
December 30, 2024
Study Completion
August 30, 2025
Last Updated
January 22, 2024
Record last verified: 2024-01