Sodium Oxybate in Patients With Chronic Fatigue Syndrome.

Ghent University Hospital (UZ)

Status and phase

Withdrawn

Phase 4

Conditions

Chronic Fatigue Syndrome

Treatments

Drug: Placebo

Drug: Sodium oxybate

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01584934

2011-006336-23 (EudraCT Number)

2012/197

Details and patient eligibility

About

Chronic fatigue syndrome (CFS) is a disabling, unexplained disorder characterized by physical and mental exhaustion. Complaints of disturbed and unrefreshing sleep are very common in CFS patients, however, the relationship between (disturbed) sleep quality and fatigue is still not fully elucidated. To evaluate the effect of sodium oxybate on fatigue and to explore the interdependence of sleep quality and fatigue in CFS, a double blind, randomized, placebo controlled cross-over trial with sodium oxybate is carried out in CFS patients.

The aim of this study is to address the issue of the effect of sodium oxybate on fatigue as a presenting symptom in chronic fatigue (CF) and CFS patients, in the absence of underlying medical or psychiatric illness. The answer to this question may shed further light on the enigmatic relationship between sleep and fatigue. We also want to investigate the effect of sodium oxybate on sleepiness and general health in the same target population.

Zero-hypothesis: there is no effect.

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients suffering from chronic, disabling, unexplained fatigue with at least 4 minor criteria for CFS, according to the 1994 Fukuda case definition;
Negatively screened for fibromyalgia syndrome(FMS) according to the American College of Rheumatology (ACR) classification criteria;
18 years or older;
65 years or less;
Female patient of childbearing potential (premenopausal female biologically capable of becoming pregnant) has a confirmed negative pregnancy test at the start of the trial and has to employ an acceptable method of birth control (double barrier method of contraception);
Written, signed and dated informed consent must be obtained from each patient;
Patient able to understand and follow the requirements of the study
Willing to abstain from taking any medication or treatment prohibited in the protocol

Exclusion criteria

FMS;
Presence of an inflammatory rheumatic disease or a painful disorder other than FMS;
Fatigue that is explained by medical or psychiatric causes;
Older than 65 or younger than 18 years of age;
Apnea/hypopnea index (AHI) > or equal to 15 on polysomnography (PSG) (exempted if receiving continuous positive airway pressure CPAP and shown good compliance)
Deficiency in succinic semialdehyde dehydrogenase;
Porphyria;
Breathing or lung problems;
Unsufficiently controlled hypertension (high blood pressure: > 140/90 mmHg);
Heart failure;
Liver or kidney problems (serum creatinine level > 2,0 mg/dl);
Presence of a seizure disorder or epilepsy;
Sodium oxybate treatment in the past;
Primary history of substance abuse (including abuse of alcohol);
Inability to withdraw from psychoactive drugs;
Current use of sedative (benzodiazepine and non-benzodiazepine GABA-ergic agonists), opioids or antidepressant medication or a drug-free interval of less than 4 weeks;
Female patient who is pregnant, lactating or has a positive pregnancy test result.
Occupation that requires night-shift work;
Willing to abstain from using alcohol