Pheochromocytoma Clinical Trial
Official title:
Diagnosis and Treatment of Pheochromocytoma
Pheochromocytoma is a tumor of the adrenal gland. This tumor is typically benign (not
cancerous) and can be cured by surgical removal. However, pheochromocytomas produce
neurohormones called cateholamines (epinephrine and norepinephrine). High levels of
catecholamines can result in high blood pressure, headaches, sweating, heart palpitations,
nausea, vomiting, and other symptoms. These tumors are considered dangerous because of their
unpredictable behavior. Patients with pheochromocytoma may experience blood pressures high
enough to cause a stroke or heart attack in patients.
This study is designed to take patients suspected of having pheochromocytoma and confirm the
diagnosis. This will be done using a variety of laboratory tests including a clonidine
suppression test and glucagon stimulation test. These tests use drugs that can stimulate or
reduce the activity of the tumor if it is present in the body.
Once a diagnosis is confirmed, patients participating in this study will undergo standard
procedures to find the exact location of the tumor and receive standard therapy for the
condition.
Patients suspected of having a pheochromocytoma will be studied via a series of tests in an attempt to ascertain biochemically whether or not they really have such a tumor. These procedures will include a standard clonidine suppression test and a standard glucagon stimulation test. Once the diagnosis has been made on the basis of biochemistry, then localization and therapy will be done via standard procedures. Measurement of plasma metanephrines on mailed samples is available for physicians who seek further evidence for the diagnosis of pheochromocytoma. ;
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