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Completed

NCT Number: NCT02055898

SWS And Daytime Functioning in Chronic FatiguE Syndrome (SAFFE)

The investigators wish to investigate whether enhancement of SWS, which is seen after a drug called sodium oxybate, reduces the impact of sleep disruption in CFS on daytime function, specifically sleepiness and mental performance. This is a safe and well-tolerated drug that is licensed for excessive daytime sleepiness (EDS) and cataplexy associated with narcolepsy.

The investigators will study 12 patients diagnosed with CFS using international diagnostic guidelines. The investigators will record overnight sleep with EEG (brainwave) measurement on the 1st and 4th nights of a 4 night period during which sodium oxybate and placebo will be taken nightly, and the investigators will measure next-day sleepiness, mental performance and fatigue, and compare drug and placebo nights.

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Key information

Age range

25 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Wellcome CRF, Imperial College, Hammersmith Campus

London, W12 0NN, United Kingdom

About this study

Chronic fatigue syndrome (CFS), characterised by chronic disabling fatigue, sleep impairment and other symptoms, is associated with neither a currently identifiable disease process nor major psychiatric illness, and has an estimated prevalence in primary care of 1-2%. Sleep impairment is common in nearly everyone with CFS, with both daytime sleepiness and unrefreshing nighttime sleep reported, and consequent impact on daytime function. It may be that fundamental regulatory processes that control sleep are disturbed in CFS, leading to different effects on sleep and daytime symptoms depending on the subject's prior sleep, daytime routine, medication and other factors. The investigators contacts with patient groups have indicated that patients are generally confident that on days when their sleep is better they perform better in the day. There is growing evidence that deep, slow wave sleep (SWS) is altered in CFS, and this may suggest impairment of build up of sleep pressure during the day.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Meeting criteria for CFS according to both the revised CDC (Fukuda 5) and Canadian diagnostic systems.
  • Aged 25-65.
  • Good grasp of the English language.

Exclusion criteria

  • Taking any of the following medication: opioids, tramadol, phenytoin, valproate, ethosuximide, benzodiazepines, zolpidem, zopiclone, zaleplon, antidepressant except <30mg amitriptyline, or any other medications likely to interact with sodium oxybate or with sleep in the opinion of the investigators.
  • Current major psychiatric disorder.
  • Unusual sleep schedule; (bedtime routines that fall outside 9 p.m. to 10 a.m.; usual time in bed > 12 hours).
  • Pregnancy, lactation or being female and not using reliable contraception.
  • Relevant abnormal clinical findings at screening visit.
  • Taken alcohol in the 24 hours before each study visit or drugs of abuse in the week before each study visit

Treatment and study plan

Sodium Oxybate

Drug

Other names: Xyrem

placebo (fresh potable water)

Other

Primary outcomes

  1. EEG Slow Wave Activity During Sleep

    Time frame: night 1

    Total power in 0.5-4Hz band in microvolts squared per Hertz (uV^2/Hz)

  2. EEG Slow Wave Activity During Sleep

    Time frame: night 4

    Total power in 0.5-4Hz band in microvolts squared per Hertz (uV^2/Hz)

  3. Daytime Sleepiness

    Time frame: Day 2

    time to fall asleep in minutes

  4. Daytime Sleepiness

    Time frame: Day 5

    time to fall asleep in minutes

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Collaborators

  • Medical Research Council

Registry information

Official study title

Slow-wave Sleep and Daytime Functioning in Chronic Fatigue Syndrome: Effects of Sodium Oxybate

Acronym: SAFFE

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Feb 5, 2014
Registry last updated
Nov 18, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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