Mortality Outcome of Controlled Hypertension

NCT ID: NCT07187596

Last Updated: 2026-01-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

1000000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-18

Study Completion Date

2026-07-14

Brief Summary

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This pooled analysis investigates death outcomes in patients with pharmacologically treated and blood pressure-controlled hypertension. Despite documented BP control, some patients still suffer fatal cardiovascular, cerebrovascular, renal, or unexplained syndromes. This study aims to synthesize available evidence across study types to identify treatment pitfalls, contributing syndromes, and non-BP factors associated with these fatal outcomes.

Detailed Description

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Although hypertension is commonly treated and controlled to target levels, fatalities still occur in some patient subgroups. This pooled review seeks to identify and analyze these populations' contributing factors, comorbidities, treatment contexts, and physiological mechanisms associated with mortality. Data will be collected from peer-reviewed studies and registries. Statistical analysis will include descriptive synthesis, subgroup tabulations, and exploratory regression.

Open-label analysis aims to investigate death outcomes among patients with treated and well-controlled hypertension by synthesizing results from published clinical trials, observational studies, and systematic reviews.

The study will statistically evaluate endpoint include fatal cardiovascular, cerebrovascular, renal, or vascular events in patients in any arm with documented blood pressure control, with clearly seen evidence.

Conditions

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Hypertension Morality Death Pre-Eclampsia Cardiovascular Diseases Stroke Renal Disease Artery Stenosis Arterial Aneurysm Arterial Rupture Maternal Death

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Human studies (RCTs, cohort, case-control, registry studies, etc.) declare participants with treated and controlled hypertension manage (regardless of drug class, duration, or comorbidity) reported mortality outcomes: all-vascular death, cardiovascular death, sudden death, etc.
* Studies in any setting (outpatient, inpatient, long-term follow-up)
* Articles in English
* Full-text available

Exclusion Criteria

* Animal specimen or parameter studies
* Uncontrolled studies (e.g., case series without control, phase I safety trials)
* No mortality endpoint reported
* Purely mechanistic studies or trials that do not address BP or survival directly
* Pediatric studies unless separated subgroup for treated hypertension is available
* Glaucoma or portal hypertension or Pulmonary Hypertension without essential/systemic hypertension outcomes
* Infection without direct declare that septic shock or immunological failure associated by vascular cause from systemic hypertension
* Secondary/post-hoc analyses that do not report original mortality data
Minimum Eligible Age

1 Minute

Maximum Eligible Age

130 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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DejthidaNathaphong

OTHER

Sponsor Role lead

Responsible Party

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Nathaphong Dejthida

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nathaphong Dejthida, MD

Role: PRINCIPAL_INVESTIGATOR

DejthidaNathaphong

Locations

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Owned study

Bangkok, , Thailand

Site Status RECRUITING

Countries

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Thailand

Central Contacts

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Nathaphong Dejthida, MD

Role: CONTACT

+66819220662

Nathaphong Dejthida, MD

Role: CONTACT

Facility Contacts

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Nathaphong Dejthida, MD

Role: primary

+66819220662

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Related Links

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Other Identifiers

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NathaphongDejthida

Identifier Type: -

Identifier Source: org_study_id

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