Skip to content

Elderly hypertension management

HOWOLD-BP (HOW to Optimize eLDly systolic Blood Pressure) Trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0003787
Enrollment
3177
Registered
2019-04-16
Start date
2019-01-15
Completion date
Unknown
Last updated
2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : Intensive treatment group vs. Standard treatment group SBP target will be different between two groups (130 mmHg in intensive group vs. 140 mmHd in standard group) Hypertension medication will

Sponsors

Chungbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) aged above 65 years 2) Hypertension patients - taking antihypertensive medications - newly diagnosed with hypertension (systolic pressure between 140 and 180 mmHg) 3) possible self-care (Activities of Daily Living (ADL) score above 100) 4) subjects with informed consent

Exclusion criteria

Exclusion criteria: 1) patients who did not agree to study 2) past medical history of secondary hypertension or suspicious secondary hypertension 3) resistant hypertension 4) orthostatic hypotensioin at screening 5) uncontrolled diabetes mellitus at screening (HbA1c above 10%) 6) end stage renal disease (on hemodialysis or eGFR less than 15 mL/min/1.73m2) 7) underwent acute coronary syndrome, cardiac surgery, or urgent percutaneous coronary intervention within recent 3 months 8) systolic heart failure with ejection fraction less than 40% 9) hypertrophic obstructive cardiomyopathy, aortic stenosis, moderate to severe valve disease, congenital heart disease 10) diagnosed with acute cerebral infarction within recent 3 months 11) diagnosed with moderate to severe retinopathy (retinal hemorrhage, visual impairment, microaneurysm) within recent 6 months 12) wasting disease, autoimmune disease, connective tissue disease 13) clinically significant liver disease or level of AST/ALT greater than 3 times upper normal range 14) uncontrolled thyroid dysfunction 15) enrolled other clinical trials within 4 months or plan to participant other clinical trials during our study 16) other reasons limiting participant or progress of study according to investigators' judgement

Design outcomes

Primary

MeasureTime frame
overall cardiovascular mortality

Secondary

MeasureTime frame
cardiovascular mortality;quality of life;cognitive function assessment;frailty assessment

Countries

Korea, Republic of

Contacts

Public ContactJu-Hee Lee

Chungbuk National University Hospital

juheelee.md@gmail.com+82-43-269-6880

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 7, 2026