NCT07447362

Brief Summary

This study aims to evaluate cardiovascular risk factors, clinical characteristics, and outcomes in adult patients attending an outpatient cardiology clinic. The research focuses on identifying predictors of adverse cardiovascular events, optimizing risk stratification, and improving preventive strategies in routine clinical practice. Data will be collected from patients receiving standard cardiology care without altering their treatment. The results are expected to contribute to better understanding of cardiovascular risk profiles and to support improvements in clinical decision-making and patient management.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
220

participants targeted

Target at P75+ for not_applicable

Timeline
2mo left

Started Jul 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress91%
Jul 2024Oct 2026

Study Start

First participant enrolled

July 24, 2024

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

February 24, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 3, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 24, 2026

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 24, 2026

Expected
Last Updated

March 3, 2026

Status Verified

February 1, 2026

Enrollment Period

2 years

First QC Date

February 24, 2026

Last Update Submit

February 27, 2026

Conditions

Keywords

Cardiovascular preventionRisk factor controlMedication adherenceClinical follow-up

Outcome Measures

Primary Outcomes (1)

  • Change in systolic blood pressure

    Change in systolic blood pressure (mmHg) measured under standardized conditions to evaluate the effect of structured clinical and pharmacological cardiovascular risk management.

    Baseline to 90 days

Secondary Outcomes (11)

  • Change in diastolic blood pressure

    Baseline to 90 days

  • Change in LDL cholesterol

    Baseline to 90 days

  • Change in HbA1c

    Baseline to 90 days

  • Change in body weight

    Baseline to 90 days

  • Change in renal function (eGFR)

    Baseline to 90 days

  • +6 more secondary outcomes

Study Arms (1)

Structured Clinical Management

EXPERIMENTAL

Participants receive structured clinical follow-up with periodic assessment of cardiovascular risk factors and adjustment of pharmacological and lifestyle management according to current clinical guidelines over a 120-day follow-up period.

Other: Structured Cardiovascular Risk Management

Interventions

Protocol-based clinical management including periodic evaluation and adjustment of antihypertensive, lipid-lowering, antidiabetic, and lifestyle interventions according to routine clinical practice guidelines.

Structured Clinical Management

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age ≥18 years
  • Presence of at least one cardiovascular risk factor (hypertension, diabetes, dyslipidemia, obesity, or smoking)
  • Receiving outpatient clinical follow-up
  • Ability to provide informed consent

You may not qualify if:

  • Severe clinical instability requiring hospitalization
  • Pregnancy
  • End-stage renal disease or dialysis
  • Inability to complete follow-up visits
  • Refusal to participate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CDIEM Medical Center - Outpatient Cardiology Clinic

Santiago, Santiago Metropolitan, Chile

RECRUITING

MeSH Terms

Conditions

HypertensionDyslipidemiasDiabetes Mellitus, Type 2ObesityOverweightTobacco UseMedication Adherence

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular DiseasesLipid Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesDiabetes MellitusGlucose Metabolism DisordersEndocrine System DiseasesOvernutritionNutrition DisordersBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsBehaviorPatient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth Behavior

Study Officials

  • José Abellán Alemán, MD, PhD

    Universidad Católica San Antonio de Murcia

    STUDY CHAIR

Central Study Contacts

Julio César Núñez Farías, MD, MSc (Cardiology)

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Model Details: Participants receive structured clinical follow-up with periodic evaluation and adjustment of standard pharmacological therapy under routine clinical practice using a before-and-after design.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Cardiologist and Principal Investigator

Study Record Dates

First Submitted

February 24, 2026

First Posted

March 3, 2026

Study Start

July 24, 2024

Primary Completion

July 24, 2026

Study Completion (Estimated)

October 24, 2026

Last Updated

March 3, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared due to privacy regulations and institutional data protection policies. De-identified aggregated results will be available through scientific publication.

Locations