Pulmonary Fibrosis & Genetic Factors Request More Information Trial Objective The purpose of this study is to investigate inherited genetic factors that play a role in the development of familial pulmonary fibrosis and to identify a group of genes that predispose individuals to develop pulmonary fibrosis. Finding the genes which play a role in pulmonary fibrosis is the first step at developing better methods for early diagnosis and improved treatment for pulmonary fibrosis. The overall hypothesis is that inherited genetic factors predispose individuals to develop pulmonary fibrosis. The study requires the following: For affected individuals, we confirm your diagnosis by reviewing your medical records. We also ask for a history questionnaire to be filled out and obtain a sample of blood or tissue for genetic studies. Unaffected family members are screened with a questionnaire, and a blood sample is obtained for genetic studies. Some family members may qualify to undergo high-resolution CT (HRCT) scan for the study. Enrollment Active Clinical Trials Currently Recruiting Who Can Participate The only requirement for this study is to have at least 2 members of your family diagnosed with Idiopathic Pulmonary Fibrosis (IPF). You may be included in this number. Age: Not Specified Gender: Any Gender Estimated Time Commitment Not Specified × Payments are intended to compensate the participant for their time and effort during the study. Payments are typically given to the participant at the end of each completed study visit. Reimbursements are intended to compensate the participant for travel-related expenses. They must be approved by the study staff and require you to turn in receipts. Travel reimbursement will vary from study to study. Payment & Reimbursement Payment: Not Provided Travel Reimbursement: Not Available Trial Contact For more information, contact: Rachel Warren 303.724.8569 Request More Information Trial Location National Jewish Main Campus, Denver, CO Trial Sponsors National Jewish Health Principal Investigators Kevin Brown, MD + × Kevin Brown, MD Chair, Department of Medicine Professor of Medicine Department of Medicine View Full Profile Patient Rating 4.9 out of 5 stars Make an Appoinment Request More Information By completing this form, you agree to learn more about this study and see if you qualify. First Name:* Last Name:* Email Address:* Phone:* I would also like to receive periodic emails with health information, news and clinical research updates from National Jewish Health: YesNo
Trial Objective The purpose of this study is to investigate inherited genetic factors that play a role in the development of familial pulmonary fibrosis and to identify a group of genes that predispose individuals to develop pulmonary fibrosis. Finding the genes which play a role in pulmonary fibrosis is the first step at developing better methods for early diagnosis and improved treatment for pulmonary fibrosis. The overall hypothesis is that inherited genetic factors predispose individuals to develop pulmonary fibrosis. The study requires the following: For affected individuals, we confirm your diagnosis by reviewing your medical records. We also ask for a history questionnaire to be filled out and obtain a sample of blood or tissue for genetic studies. Unaffected family members are screened with a questionnaire, and a blood sample is obtained for genetic studies. Some family members may qualify to undergo high-resolution CT (HRCT) scan for the study.