A Randomized, Double-Blind, Placebo-Controlled, Multicenter Trial of the Safety and Efficacy of Ceftriaxone and Doxycycline in the Treatment of Patients With Seronegative Chronic Lyme Disease

Inclusion Criteria: You may be eligible for this study if you: Are at least 18 years of age. Are seronegative for antibodies against B. burgdorferi antigens by Western Blot at enrollment. Have documented history of acute Lyme disease. Have had a rash (erythema migrans) that resembles a bullseye. This skin aberration usually occurs after a tick bite in late spring, summer, or early fall and is sometimes accompanied by fatigue, fever, headache, mild stiff neck, arthralgia or myalgia. Have had one or more clinical features typical of Lyme disease acquired in the United States (see technical summary) Have had one or more of the following symptoms and conditions that have persisted for at least 6 months (but less than 12 years) and are not attributable to another cause or condition: a) widespread musculoskeletal pain and fatigue that began coincident with or within 6 months following initial infection with B. burgdorferi. b) certain neurologic symptoms including memory impairment and nerve pain, beginning within 6 months following initial infection with B. burgdorferi. Have had a physician-documented history of prior antibiotic treatment with a currently recommended antibiotic regimen. Exclusion Criteria: You will not be eligible for this study if you: Have previously enrolled in this study. Are pregnant, lactating, or unable to use birth control measures during the treatment period of this study. Are taking chronic medication that could interfere with evaluation of symptoms. Are taking or have taken various medications that could interfere with the evaluation of symptoms (see technical summary). Are hypersensitive to ceftriaxone or doxycycline. Have active inflammatory synovitis. Have another disease that could account for symptoms of acute Lyme disease. Have another serious or active infection. Are unable to tolerate an IV. Have tested positive for Borrelia DNA in plasma or cerebrospinal fluid at the time of initial evaluation for study. Have tested seropositive by Western Blot (these patients may be offered enrollment in seropositive study).