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Study to Evaluate the Efficacy and Safety of TEL/AML/CTD in Elderly Patients With Essential Hypertension

← catalyst calendar

NCT06041529

Sponsored by Yuhan Corporation (industry) · 000100.KS — their whole pipeline →.

Phase
Phase 4
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
198actual
Sites
15
Country
South Korea

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-10-18actualWhen the study began enrolling
Primary completion2026-02-28estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-02-28estimatedThe whole study's end, after follow-up
First posted2023-09-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Essential Hypertension

Interventions

  • Drug: Telmisartan/Amlodipine/Chlorthalidone 40/5/12.5 mg — also filed as Truset 40/5/12.5mg
  • Drug: Telmisartan/Amlodipine/Hydrochlorothiazide 40/5/25 mg — also filed as Twynsta 40/5 mg, Dichlozid 25 mg

Primary outcome

what the primary-completion date above is the date OF
Mean Systolic Blood Pressure (MSBP) in nighttime
measured Week 8

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