Chronic fatigue syndrome (CFS) is a serous health problem in the United States, affecting at least 3 of every 1,000 patients sen in general medicine clinics. It is estimated that the prevalence rate in the United States is 4 - 10/100,000 persons. No effective treatment has been identified. Recent observations suggest a strong association between CFS and a treatable disorder in the regulation of blood pressure known as neurally mediated hypotension. In a small unblinded studie, treatment with fludrocortisone and other medications directed against neurally mediated hypotension has appeared to be beneficial., with 40% of treated patients reporting an almost complete resolution of symptoms and another 30% reporting some improvement.
The specific aim of this randomized double blind, placebo controlled trial is to determine whether fludrocortisone is efficacious for those with CFS. They study will randomize 100 adults with CFS to receive either fludrocotisone or placebo. The patients will be entered either through Johns Hopkins Hospital or through NIH. Before, during, and for 2 weeks after treatment, participants will complete self-assessment forms. The primary indicator of efficacy will be a 15 point improvement (on a scale of 1 to 100) in the general sense of well being score. Eligibility criteria include persons 18-49 years of age who satisfy the 1994 CDC criteria for CFS, and have undergone a medical evaluation to exclude other causes of CFS, and have hpotension provoked during stage 1 or 2 of an pright tilt table test, perfomed as part of the study.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000812-01
Application #
6160803
Study Section
Special Emphasis Panel (LCI)
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code