To Study the Mortality Outcome of Controlled Blood Pressure Participants
HTN-Mort
Mortality Outcome of Controlled Hypertension in Randomized Controlled or Open-label Study Intentionally Directed Intervention Effect Blood Pressure: A Systematic Review and Meta-Analysis
1 other identifier
observational
100
1 country
1
Brief Summary
Despite advances in antihypertensive therapy, some patients with well-controlled blood pressure still experience fatal outcomes. This paradox raises critical questions about the efficacy of blood pressure-targeted interventions and whether BP control alone ensures survival. This systematic review and meta-analysis aims to evaluate all-cause mortality and cardiovascular death among hypertensive patients who achieved BP targets in RCTs or open-label trials. To determine whether achieving controlled blood pressure through intentional intervention (pharmacological or procedural) in RCTs or open-label studies reduces mortality (all-cause and cardiovascular) in hypertensive patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2025
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
July 1, 2025
CompletedFirst Submitted
Initial submission to the registry
July 6, 2025
CompletedFirst Posted
Study publicly available on registry
July 16, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 1, 2027
April 13, 2026
April 1, 2026
1.5 years
July 6, 2025
April 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
All-cause mortality
All cause mortality by controlable hypertension treatment
100 year
Study Arms (2)
Antihypertensive treatment
Participants assigned to interventions (pharmacological, device-based, or lifestyle) directed at lowering blood pressure or Antihypertensive agents, Blood pressure-lowering treatment, Antihypertensive therapy.
Control/Comparator
Participants receiving placebo, standard of care, or no intervention
Interventions
Any intervention (pharmacological, device-based, lifestyle) intentionally directed at lowering BP Control groups receiving placebo, standard of care, or no intervention
Eligibility Criteria
Adults ≥18 years with diagnosed hypertension Blood pressure controlled at target values defined by the study (e.g., \<140/90 mmHg or \<130/80 mmHg) Any comorbidity allowed unless the study focuses on pregnancy or pediatric population
You may qualify if:
- Adults ≥18 years with diagnosed hypertension
- Blood pressure controlled at target values defined by the study (e.g., \<140/90 mmHg or \<130/80 mmHg)
- Any comorbidity allowed unless the study focuses on pregnancy or pediatric population
You may not qualify if:
- Observational or retrospective studies
- Pediatric or pregnant participants
- Case reports, editorials, or conference abstracts without full data
- Studies not reporting mortality outcomes separately for controlled BP
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Nathaphong
Bangkok, 10110, Thailand
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nathaphong Dejthida, MD
DejthidaNathaphong
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 6, 2025
First Posted
July 16, 2025
Study Start
July 1, 2025
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
February 1, 2027
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, CSR, ANALYTIC CODE