Study Results
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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RECRUITING
1000000 participants
OBSERVATIONAL
2025-09-18
2026-07-14
Brief Summary
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Detailed Description
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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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Study Design
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OTHER
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Studies in any setting (outpatient, inpatient, long-term follow-up)
* Articles in English
* Full-text available
Exclusion Criteria
* 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
1 Minute
130 Years
ALL
No
Sponsors
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DejthidaNathaphong
OTHER
Responsible Party
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Nathaphong Dejthida
Principle Investigator
Principal Investigators
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Nathaphong Dejthida, MD
Role: PRINCIPAL_INVESTIGATOR
DejthidaNathaphong
Locations
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Owned study
Bangkok, , Thailand
Countries
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Central Contacts
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Facility Contacts
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Related Links
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PROSPERO registry
Other Identifiers
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NathaphongDejthida
Identifier Type: -
Identifier Source: org_study_id
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