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CHACO Study: Control of Arterial Hypertension in Colombian Patients

CHACO Study: Control of Arterial Hypertension in Colombian Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04094714
Acronym
CHACO
Enrollment
1100
Registered
2019-09-19
Start date
2019-06-27
Completion date
2024-07-31
Last updated
2019-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Brief summary

Epidemiological study (cross-sectional study) in order to determine the patients who present an adequate control of the Blood Pressure (BP), in a population of Colombian patients diagnosed with Arterial Hypertension (AH) and who are under pharmacological treatment.

Detailed description

OBJECTIVE: To determine the proportion of patients who present an adequate control of the Blood Pressure (BP), in a population of Colombian patients diagnosed with Arterial Hypertension (AH) and who are under pharmacological treatment. MATERIALS AND METHODS: Epidemiological study (cross-sectional study), multicentre type, in patients older than 18 years with prior diagnosis of AH in Colombia. The blood pressure control will be evaluated as the main variable (only one single blood pressure check in the doctor's office). Other secondary variables to evaluate are: demographical analysis, type (s) of antihypertensive treatment (s) used in patients, level of BP control, adverse events associated with antihypertensive treatment, comorbidities and risk factors, adherence, perception about the possible benefits of the use of combined therapy in mono-tablet versus multi-tablet. The analysis will be carried out from two perspectives: A first descriptive approach and a second analytical approach, with a level of significance of 5%.

Interventions

None listed

Sponsors

Scandinavia Pharma
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Prior diagnosis of Arterial Hypertension (AH) ≥ 3 months before * Patients who are under pharmacological treatment of AH ≥ 3 months before

Exclusion criteria

* The patient has rejected the participation in the study. * Patients who, in the judgment of the Investigator, do not understand or are not willing to adequately answer the questions. * Mental or psychiatric illness that, in the judgment of the investigator, does not allow adequate information to be obtained.

Design outcomes

Primary

MeasureTime frameDescription
Patients with adequate control of the Blood Pressure (BP)It will be evaluated in each patient (only once, at the time of the interview) throughout the study which is estimated to last 3 years.Proportion of patients who present an adequate control of the Blood Pressure (BP)

Secondary

MeasureTime frameDescription
Demographic analysisIt will be evaluated in each patient (only once, at the time of the interview) throughout the study which is estimated to last 3 years.Characterization of patients
Treatment analysisIt will be evaluated in each patient (only once, at the time of the interview) throughout the study which is estimated to last 3 years.Characterization of treatment (s) used
Personal history of diseasesIt will be evaluated in each patient (only once, at the time of the interview) throughout the study which is estimated to last 3 years.Evaluation of personal history of diseases
Adverse Events related with the treatmentIt will be evaluated in each patient (only once, at the time of the interview) throughout the study which is estimated to last 3 years.Adverse events associated with the treatment (s)

Countries

Colombia

Contacts

Primary ContactJavier Castillo, Dr
jcastill@scandinavia.com.co+571-6461700
Backup ContactFerrari Claudio, Dr
cferrari@scandinavia.com.co+571-6461700

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026