Overview

Autonomic Nervous System and Chronic Fatigue Syndrome

Status:
Completed
Trial end date:
2017-01-01
Target enrollment:
0
Participant gender:
All
Summary
The investigators propose to test the hypothesis that the sympathetic nervous system contributes to the cardiovascular and inflammatory abnormalities present in the chronic fatigue syndrome (CFS) and, in particular in the subset of patients characterized by postural tachycardia syndrome (POTS). CFS and POTS are seen mostly in otherwise normal young women, and are the cause of significant disability. A substantial proportion of patients referred for evaluation of POTS met diagnostic criteria for CFS and, conversely, a subset of patients referred for treatment for CFS have POTS. The investigators hypothesize that sympathetic activation underlies the pathophysiology of patients in whom CFS and POTS overlap (CFS-P).
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Vanderbilt University
Vanderbilt University Medical Center
Treatments:
Methyldopa
omega-N-Methylarginine
Trimethaphan
Trimethaphan camsylate
Criteria
Inclusion Criteria:

- Meet CDC diagnostic criteria of CFS (Fukuda et al., 1994)

- Meet diagnostic criteria of POTS (Raj et al., 2005)

- Age between 18-65 years

- Male and female are eligible (although the majority of patients with CFS-P are female)

Exclusion Criteria:

- Presence of medical conditions that can explain postural tachycardia syndrome (e.g.,
dehydration, medications)

- Presence of medical or psychiatric conditions known to cause fatigue (Fukuda et al.,
1994). Inability to give, or withdrawal of, informed consent

- Inability to acquire or maintain adequate long-term intravenous access (peripheral
indwelling catheter, PIC)

- Pregnancy

- Other factors which in the investigator's opinion would prevent the subject from
completing the protocol

- Patients who are bedridden or chair-ridden