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Sponsored by: |
National Heart, Lung, and Blood Institute (NHLBI) |
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Information provided by: | National Institutes of Health Clinical Center (CC) |
ClinicalTrials.gov Identifier: | NCT00001869 |
Pulmonary lymphoangioleiomyomatosis (LAM) is a rare destructive lung disease typically affecting women of childbearing age. Currently, there is no effective therapy for the disease and the prognosis is poor.
In order to better study this disease, the National Heart, Lung, and Blood Institute (NHLBI) has developed a registry to keep an official record of patients diagnosed with LAM. This research project will collect data from 6 health care centers as well as outside physicians. Researchers hope to provide valuable information about the rate of lung destruction and quality of life in patients with LAM.
Patients participating in this study will be followed for 5 years. Tissue collected from these patients may contribute to the development of future studies on the disease processes of LAM.
Condition |
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Leiomyomatosis |
Study Type: | Observational |
Official Title: | Lymphangioleiomyomatosis (LAM) Registry |
Estimated Enrollment: | 400 |
Study Start Date: | December 1998 |
Estimated Study Completion Date: | April 2003 |
LAM is a rare disease that predominantly affects women of child-bearing age. To study in more detail this rare disease, this multi-center project will establish a registry of persons with LAM. By combining data from 6 centers and outside physicians, this study may yield valuable information regarding the rate of decline in pulmonary function and quality of life in individuals with LAM. These patients will be followed over a five-year period. Tissue collected from study participants may facilitate future studies into the molecular basis of LAM.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Informed consent must be obtained from the patient.
Patients must be female.
Patients must be age 18 or older.
Patients with prevalent and incident cases are eligible.
Patients with the presence or absence of underlying diagnosis or evidence of Tuberous Sclerosis Complex (TSC) are eligible.
Patients must have a diagnosis of LAM confirmed by any of the following criteria:
Lung biopsy (transbronchial, surgical, transthoracic) judged to be diagnostic by the Tissue Core pathologists;
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Biopsy of lymph node or other mass judged to be diagnostic by the Tissue Core pathologists;
OR
High resolution CT scan of the chest which is judged to be diagnostic of LAM with a high degree of certainty by all three of the expert radiologists making up the Imaging Core.
Patients may be enrolled in other protocols.
Study ID Numbers: | 990020, 99-H-0020 |
Study First Received: | November 3, 1999 |
Last Updated: | March 3, 2008 |
ClinicalTrials.gov Identifier: | NCT00001869 |
Health Authority: | United States: Federal Government |
Progesterone Pulmonary Function Tests Pneumothorax Oopherectomy |
High Resolution CT Tuberous Sclerosis Complex Lymphangioleiomyomatosis (LAM) |
Myofibroma Immunoproliferative Disorders Progesterone Leiomyomatosis Lymphangiomyoma Sclerosis Leiomyoma Bourneville syndrome |
Lymphangioleiomyomatosis Neoplasms, Connective and Soft Tissue Lymphatic Diseases Tuberous Sclerosis Tuberous sclerosis Lymphoproliferative Disorders Pneumothorax |
Lymphatic Vessel Tumors Neoplasms, Muscle Tissue Neoplasms Neoplasms by Histologic Type Immune System Diseases |