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Completed

NCT Number: NCT03000777

Oral Melatonin Plus Zinc Supplementation in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME)

The purpose of this study is to evaluate the effects of oral melatonin plus zinc supplementation in relieving self-reported fatigue in CFS/ME

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Key information

About this study

Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) is a complex medical condition, characterized by severe disabling fatigue with no known cause, no established diagnostic tests, and no universally effective treatment. No studies have evaluated symptomatic treatment using oral melatonin plus zinc supplementation in CFS/ME. The primary endpoint was to assess the effect of melatonin plus zinc supplementation on self-reported fatigue. Secondary measures included self-reported outcomes of sleep problems, anxiety/depression, dysautonomia, QoL and side-effects during treatment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • CFS patient based on the 1994 Centers for Disease Control and Prevention/Fukuda definition.
  • Patient who provided signed informed consent.

Exclusion criteria

  • Patients who are participating in another clinical trial of the same or different nature previous 30 days prior to inclusion.
  • Any subject that, in the judgment of the investigator, is not able to follow the instructions or to perform a good completion of the treatment.
  • Subjects that do not provide signed informed consent.
  • Patients who are receiving any of the drugs or products that may interfere with the results, and whose withdrawal could be a relevant medical problem.
  • Patients receiving oral anticoagulants.
  • Pregnancy or lactation
  • Patients with hypersensitivity to melatonin and/or zinc.

Treatment and study plan

melatonin plus zinc

Dietary Supplement

Melatonin 1 mg plus Zinc 10 mg o.d. 1 hour before going to bed during 16 weeks

Other names: MelatoZinc

Placebo

Other

Isomaltose o.d. 1 hour before going to bed during 16 weeks

Other names: Control

Primary outcomes

  1. To evaluate relieving self-reported fatigue using the Fatigue Impact Scale 40-items (FIS 40) questionnaire after oral melatonin plus zinc administration

    Time frame: within the first 16 weeks (plus 4 weeks with no treatment)

Secondary outcomes

  1. Side effects during treatment.

    Time frame: within the first 16 weeks (plus 4 weeks with no treatment)

  2. Self-reported sleep quality through the Pittsburgh Sleep Quality Index (PSQI) questionnaire.

    Time frame: within the first 16 weeks (plus 4 weeks with no treatment)

  3. Self-reported anxiety/depression through the Hospital Anxiety and Depression Scale (HADS) questionnaire.

    Time frame: within the first 16 weeks (plus 4 weeks with no treatment)

  4. Self-reported dysautonomia using the Composite Autonomic Symptom Score 31-items (COMPASS 31) questionnaire.

    Time frame: within the first 16 weeks (plus 4 weeks with no treatment)

  5. Self-reported QoL through the Short Form Health Survey 36-items (SF-36) questionnaire.

    Time frame: within the first 16 weeks (plus 4 weeks with no treatment)

Sponsors and collaborators

Lead sponsor

Laboratorios Viñas, S.A.

Industry

Collaborators

  • Hospital Vall d'Hebron
  • Laboratorio Echevarne

Registry information

Official study title

An Unicentric, Double-blind, Placebo Controlled, Phase IV Clinical Trial of Oral Melatonin Plus Zinc to Evaluate Relieving Self-reported Fatigue in CFS/ME

Acronym: MELATOZINC

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Dec 22, 2016
Registry last updated
Aug 9, 2018

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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