Alexandria main university hospital
Alexandria, Asafra, 11511, Egypt
NCT Number: NCT07343401
Impact of Immunosuppressive Therapy for Sarcoidosis on Lymphoma Development
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Alexandria, Asafra, 11511, Egypt
This is a prospective observational cohort study to be conducted in the Chest Diseases Department, Alexandria Main University Hospital. A total of 40 adult patients (≥16 years) with biopsy-proven sarcoidosis will be consecutively recruited between December 2024 and December 2025. All patients will be either newly starting or continuing immunosuppressive therapy for sarcoidosis. The treatment regimen-systemic corticosteroids, conventional steroid-sparing agents (methotrexate, azathioprine, or mycophenolate), or biologics (anti-TNF agents)-will be recorded but not altered by study design. Each patient will be followed prospectively for 12 months from enrollment.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients with a prior history of lymphoma or other active malignancy, HIV infection, or other primary immunodeficiency will be excluded.
-
sarcoidosis diagnosis by lymph node biopsy excisiona or bronchoscopic
Time frame: 12 MONTHS
LYMPH NODE BIOPSY EITHER EXCISIONAL OR BRONCHOSCOPIC
Time frame: 12 months
lymph node biopsy excisional or bronchoscopic
Alexandria University
Other
Impact of Immunosuppressive Therapy of Sarcoidosis on Lymphoma Development
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03793439
Hemic and Lymphatic Diseases, Hypersensitivity
Portland, Oregon, United States
View Trial DetailsNCT07613216
Behavior, Cardiovascular Diseases
Norfolk, Virginia, United States
View Trial DetailsNCT06853834
Hemic and Lymphatic Diseases, Hypersensitivity
Lucknow, Uttar Pradesh, India
View Trial DetailsNCT05415137
Fibrosis, Granuloma
Birmingham, Alabama, United States
View Trial Details