To Study the Mortality Outcome of Controlled Blood Pressure Participants

NCT ID: NCT07067632

Last Updated: 2026-01-21

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-07-01

Study Completion Date

2027-02-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Sensitivity Analyses Excluding high risk of bias studies

Excluding short follow-up (\<1 year)

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Valid MeSH Conditions Hypertension (HTN)

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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.

Antihypertensive treatment

Intervention Type DRUG

Any intervention (pharmacological, device-based, lifestyle) intentionally directed at lowering BP

Control groups receiving placebo, standard of care, or no intervention

Control/Comparator

Participants receiving placebo, standard of care, or no intervention

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Antihypertensive treatment

Any intervention (pharmacological, device-based, lifestyle) intentionally directed at lowering BP

Control groups receiving placebo, standard of care, or no intervention

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

device-based blood pressure lowering lifestyle modification

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion 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

Exclusion Criteria

* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

DejthidaNathaphong

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Nathaphong Dejthida, MD

Role: PRINCIPAL_INVESTIGATOR

DejthidaNathaphong

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Nathaphong

Bangkok, , Thailand

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Thailand

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Nathaphong Dejthida

Role: CONTACT

+66819220662

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Nathaphong Dejthida, MD

Role: primary

+66819220662

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

DejthidaNathaphong

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Moxonidine Effects on Neuropeptide Y
NCT05147753 COMPLETED PHASE4