Registry of Chronic Venous Disease in Brazil
Brazilian Registry of Chronic Venous Disease - Risk Factors, Comorbidities, Clinical and Surgical Treatment: BRAVO Study
This study is collecting information from people in Brazil with chronic venous disease to understand its causes, related health issues, and how it's treated, so that better care can be provided.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 650 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Sao Paulo General Hospital Academic / other |
| Locations | 1 site (Sao Paulo) |
| Trial ID | NCT06683586 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather national data on chronic venous disease (CVD) in Brazil, focusing on its risk factors, comorbidities, and treatment approaches. CVD is a prevalent condition characterized by symptoms such as edema and venous ulcers, significantly affecting patients' quality of life. The study will collect data from patients diagnosed with CVD to better understand its epidemiological characteristics and the socioeconomic burden it imposes. By identifying lifestyle factors and other risk contributors, the research seeks to inform better management strategies for this condition.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older diagnosed with chronic venous disease.
Not a fit: Patients who are pregnant or unwilling to participate in the study will not benefit from this research.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of chronic venous disease in Brazil, ultimately enhancing patient care.
How similar studies have performed: While there is limited recent data on CVD in Brazil, previous studies have highlighted the prevalence of this condition, indicating a need for updated research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients of both sexes diagnosed with chronic venous disease; * Age equal to or greater than 18 years; * Signature of the informed consent form. Exclusion Criteria: * Non-agreement to participate in the study; * Pregnant women.
Where this trial is running
Sao Paulo
- Hospital das Clinicas HCFMUSP — Sao Paulo, Brazil (Recruiting)
Study contacts
- Principal investigator: Rodrigo Kikuchi, MD, PhD — Santa Casa de Misericordia de Sao Paulo
- Study coordinator: Vinicius C Quintao, MD, MSc, PhD
- Email: vinicius.quintao@hc.fm.usp.br
- Phone: +55 11 97127-3950
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.