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Immune-Pineal Axis Function in Fibromyalgia

Phase II Role of Immune-pineal Axis in Fibromyalgia: Noradrenergic Modulation and Chronotherapeutic Aspects

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02041455
Enrollment
66
Registered
2014-01-22
Start date
2010-06-30
Completion date
2014-03-31
Last updated
2014-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fibromyalgia

Keywords

Fibromyalgia, Melatonin, Amitriptylin, Imune-pineal axis

Brief summary

Fibromyalgia is a common condition in clinical medical practice, characterized by diffuse musculoskeletal pain. Sleep disorders, chronic fatigue, depression, intestinal disorders and headache are also commonly associated with the syndrome . Although the etiology of this syndrome is not well defined yet, it means involve multiple mechanisms, including low levels of serotonin, increased substance P in cerebrospinal fluid and altered circadian variation in sympathetic - parasympathetic balance, consistent with changes in sympathetic hyperactivity at night . The immune - pineal system, formed by the integration of the adrenergic and immune systems pineal gland, appears to be involved in the genesis of the dysfunctions found in fibromyalgia. Melatonin is secreted by the pineal gland and has promoter activity of sleep. Studies show that melatonin and its precursors , serotonin and tryptophan are reduced in patients with fibromyalgia. The present study aims to evaluate the relationship of immune - pineal system in the process of fibromyalgia , since dysfunction of this axis appears to govern the cascading events that participate in the pathophysiological process of this disease.

Interventions

DRUGMelatonin and Placebo
DRUGAmitriptyline and Placebo
DRUGMelatonin and Amitriptylin

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Women 18-65 years old * Fibromyalgia according to the criteria of the American College of Rheumatology (Wolfe 2010) * Sign the informed consent * Patients can take medication for chronic pain ( antidepressants , antiepileptics, for example), since there are at least two months

Exclusion criteria

* patients who did not understand the Portuguese * diagnosis of malignancies, severe psychiatric disorders , sleep disorders not related to fibromyalgia (apnea , sleepwalking , restless leg syndrome), Alzheimer's disease or any disease (rheumatologic, neurological, etc.) that can modify the evaluations or outcomes * alcohol abuse or drug addiction * patients who are performing acupuncture * BMI greater than 35 ( BMI = body mass index) . * Patients with history of allergy to amitriptyline or/and melatonin or any other contraindication for the use of these drugs

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in pain on Fibromyalgia Impact Questionnaire (FIQ) at week 6Baseline, week 6
Change from Baseline in Pain Pressure Threshold (PPT) at week 6Baseline, week 6Pain Pressure Threshold by Fischer algometer on the tender points.
Change from Baseline Brain-derived neurotrophic factor at week 6Baseline, week 6

Secondary

MeasureTime frameDescription
Change from Baseline of the Pittsburgh Sleep Quality Index (PSQI) at week 6Baseline, week 6
Change from Baseline of the Pain Catastrophizing Scale at week 6Baseline; week 6Catastrophic thinking related to pain

Countries

Brazil

Contacts

Primary ContactWolnei Caumo, PhD
caumo@cpovo.net555133598083

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026