Skip to content

Registry for advanced sarcoidosis (ReAS)

Registry for advanced sarcoidosis (ReAS) - ReAS

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45613
Enrollment
100
Registered
2017-02-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

pulmonary sarcoidosis

Interventions

pulmonary sarcoidosis
Quality of life
Registry

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: * Patients with diagnosis of sarcoidosis based on ATS/WASOG criteria 22 * Age * 18 years. * Life expectancy of at least 2 years. * Pulmonary function tests (spirometry) within one month of entry or willing to under pulmonary function testing on the day of study enrollment * Sarcoidosis as characterized as either advanced or non-advanced (see protocol for definition of advanced disease) * Subjects must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.

Exclusion criteria

Exclusion criteria: * Subjects with a medical disorder, condition, or history of such that would impair the subject*s ability to participate or complete this study in the opinion of the investigator * Inability to comply with the protocol and/or not willing or not available for follow-up assessments.

Design outcomes

Primary

MeasureTime frame
Disease development of advanced and non-advanced sarcoidosis.

Secondary

MeasureTime frame
Quality of life for patients with advanced and non-advanced sarcoidosis as assessed using questionairs

Countries

United States of America

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)