HypErsensitiVity PneumonITis: DiseAse Progression Characterization. An International Multicentric Prospective Observational Study

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

EVITA is a multicentric Latin-American prospective cohort on chronic hypersensitivity pneumonitis. EVITA's objective is to identify phenotypes and/or endotypes associated with different disease trajectories measured primarily by forced vital capacity (FVC) during a 24 month follow-up period. Other secondary measures of disease progression will also be investigated such as imaging, time to death or lung transplantation, and patient-reported outcomes

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

⁃ Adult outpatient subjects (18 years old or older) that fulfill the 2020 ATS/JRS/ALAT diagnostic criteria of HP of at least moderate confidence (70% confidence or more).

⁃ Willingness to undergo the evaluations proposed in this protocol

⁃ HP diagnosis within the last 24 months

⁃ Presence of radiological or histological fibrosis:

• a. Radiological fibrosis consists of unequivocal fine or coarse reticulation with architectural lung distortion and/or traction bronchiectasis and/or honeycomb.

• b. Unequivocal histopathological fibrosis evidenced on lung specimens

Locations
Other Locations
Argentina
Hospital Prov de Tórax Dr. A. Cetrángolo
ACTIVE_NOT_RECRUITING
Bueno Aires
Instituto de Rehabilitacion Psicofisica
ACTIVE_NOT_RECRUITING
Buenos Aires
University of Buenos Aires
ACTIVE_NOT_RECRUITING
Buenos Aires
Brazil
University Hospital HU Professor Polydoro - Federal University of Santa Catarina
ACTIVE_NOT_RECRUITING
Florianópolis
Centro EDUMED
ACTIVE_NOT_RECRUITING
Paraná
LABOX - Federal University of Santa Catarina
ACTIVE_NOT_RECRUITING
Santa Catarina
LAPOGE - Federal University of Santa Catarina
ACTIVE_NOT_RECRUITING
Santa Catarina
Hospital do Servidor Estadual de Sao Paulo (IAMPSE)
RECRUITING
São Paulo
InCor - Medical School of the University of Sao Paulo
NOT_YET_RECRUITING
São Paulo
Chile
Instituto Nacional del Tórax
NOT_YET_RECRUITING
Santiago
Contact Information
Primary
Leticia Kawano-Dourado (PI), MD
ldourado@hcor.com.br
+551130536611
Backup
Samara Pinheiro (Project Manager)
scgomes@hcor.com.br
Time Frame
Start Date: 2022-06-20
Estimated Completion Date: 2026-03-01
Participants
Target number of participants: 150
Treatments
Hypersensitivity pneumonitis
see elegibility criteria
Sponsors
Leads: Hospital do Coracao
Collaborators: Boehringer Ingelheim, Centro Rossi, Buenos Aires, Argentina

This content was sourced from clinicaltrials.gov