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LDN and tDCS in Fibromyalgia

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
Low-Dose Naltrexone
Transcranial Direct Current Stimulation
Placebo
Sham Transcranial Direct Current Stimulation
Sponsored by
Centro Universitario La Salle
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring tDCS, LDN, Transcranial Direct Current Stimulation, Low Dose Naltrexone

Eligibility Criteria

8 Years - 65 Years (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • signed the consent form
  • women from 18 to 65 years
  • confirmed diagnosis of fibromyalgia according 2016 American College of Rheumatology criteria
  • read and write
  • pain higher than 6 in the Visual Analogue Scale (VAS), in the last 3 months
  • chronic stable treatment in the last 3 months.

Exclusion Criteria:

  • in use of opioid drugs;
  • pregnancy or not using anticontraceptive
  • history of alcohol or drug abuse in the last 6 months
  • history of neurological pathologies
  • history of arrhythmia
  • history of use of drugs that might change vascular response
  • history of head trauma
  • history of neurosurgery
  • decompensated systemic diseases or chronic inflammatory diseases (lupus, rheumatoid arthritis, Sjogren syndrome, Reiter syndrome)
  • history of non-compensated hypothyroidism
  • personal history of cancer.

Sites / Locations

  • Universidade La Salle

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Sham Comparator

Placebo Comparator

Other

Arm Label

LDN + tDCS

LDN + Sham tDCS

Placebo + tDCS

Placebo + Sham tDCS

Arm Description

Low Dose Naltrexone and Transcranial Direct Current Stimulation

Low Dose Naltrexone and Sham Transcranial Direct Current Stimulation

Placebo and Transcranial Direct Current Stimulation

Placebo and Sham Transcranial Direct Current Stimulation

Outcomes

Primary Outcome Measures

Pain in VAS
Visual Analogue Scale (VAS) that goes from 0 cm (without pain) to 10cm (worst pain).

Secondary Outcome Measures

Depressive symptoms
Beck Depression Inventory (BDI-II) that goes from 0 (without depressive symptoms) to 63 (worst depressive symptoms)
Anxiety levels
State-Trait Anxiety Inventory (STAI) divided into state anxiety (from 0 to 52, the higher the worse) and trait anxiety (from 0 to 48, the higher the worse)
Pain Catastrophizing Thought
Pain Catastrophizing Scale (PCS): divided into rumination (from 0 to 16, the higher the worse), magnification (from 0 to 12, the higher the worse) and hopelessness (from 0 to 24, the higher the worse). Total goes from 0 to 52, the higher the worse
Profile of Chronic Pain
Profile of Chronic Pain Scale (PCP:S): divided into Frequency and Intensity of Pain (from 0 to 30, the higher the worse), Pain Effect in Activities (from 0 to 36, the higher the worse) and Pain Effect in Emotions (from 0 to 25, the higher the worse)
Pain Pressure Threshold
Pain Pressure Threshold (PPT) measured using an electronic algometer applied in the right forearm; and patients need to report the first pain sensation (minimum pain) and maximum pain. Threshold goes from 0 to the maximum value the patient can hold, the higher the value, better is the result
Conditioned Pain Modulation
Conditioned Pain Modulation (CPM) with an algometer (PPT task), the patient informed when felt a pain equal to 6 in the VAS. This pain level was applied in the right forearm for 30 seconds, while the left forearm (non-dominant hand) was submerged in water from 0˚C to 1.5˚C; after 30s, patients reported their pain in each of the arms. CPM = left forearm VAS - 6. (from -4 to 6, the value must be as closest to -4 as possible, meaning the higher the worse)
Serum BDNF
Blood sample collected and centrifuged, the supernatant aliquoted for BDNF analysis using ELISA technique, according to manufacturer's instructions (values start in 0, patients with fibromyalgia usually have higher levels of serum BDNF, therefore the higher the worse)

Full Information

First Posted
July 25, 2020
Last Updated
August 3, 2020
Sponsor
Centro Universitario La Salle
Collaborators
Hospital de Clinicas de Porto Alegre
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1. Study Identification

Unique Protocol Identification Number
NCT04502251
Brief Title
LDN and tDCS in Fibromyalgia
Official Title
Association of Low Doses of Naltrexone and Transcranial Direct Current Stimulation in Fibromyalgia: Randomized Clinical Trial, Blind, Controlled With Placebo
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
August 1, 2019 (Actual)
Study Completion Date
July 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Universitario La Salle
Collaborators
Hospital de Clinicas de Porto Alegre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Fibromyalgia is a complex generalized and diffuse musculoskeletal chronic pain; and pharmacological approaches are widely used to relieve pain and increase life quality. In this context, low-dose naltrexone (LDN) was able to increase nociceptive threshold in patients with fibromyalgia. Moreover, non-pharmacological techniques, like Transcranial Direct Current Stimulation (tDCS), have been shown effective for pain management. This study aims to evaluate the analgesic and neuromodulatory effect of combined LDN followed by tDCS in fibromyalgia patients. This is a randomized, double-blinded, parallel, placebo/sham-controlled trial, in which 92 (10% loss) women with fibromyalgia will be included included and signed the informed consent. Patients will be allocated into 4 groups: tDCS+LDN (n=21), Sham-tDCS+LDN (n=22), tDCS+Placebo (n=22), and Sham-tDCS+Placebo (n=21). LDN or placebo (p.o.) intervention lasts 26 days, in the last five, tDCS will be applied (sham or active, 20min, 2mA). Questionnaires assessed are: Sociodemographic, Visual Analog Pain Scale (VAS), Pain Catastrophizing Scale (PCS), State-Trait Anxiety Inventory (STAI), Fibromyalgia Impact Questionnaire (FIQ), Beck Depression Inventory (BDI-II), Chronic Pain Profile Scale (CPP). Also, pain measures were taken: Pain Pressure Threshold (PPT) and Conditioned Pain Modulation (CPM). Blood samples will be collected to analyze Brain Derived Neurotrophic Factor (BDNF) serum levels.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
tDCS, LDN, Transcranial Direct Current Stimulation, Low Dose Naltrexone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
A randomized, double-blinded, parallel, controlled with placebo and sham stimulation, clinical trial.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
This is a double-blinded study, in which the participants and the outcomes assessor, who is the same as the investigator and the care provider, are blinded
Allocation
Randomized
Enrollment
92 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LDN + tDCS
Arm Type
Active Comparator
Arm Description
Low Dose Naltrexone and Transcranial Direct Current Stimulation
Arm Title
LDN + Sham tDCS
Arm Type
Sham Comparator
Arm Description
Low Dose Naltrexone and Sham Transcranial Direct Current Stimulation
Arm Title
Placebo + tDCS
Arm Type
Placebo Comparator
Arm Description
Placebo and Transcranial Direct Current Stimulation
Arm Title
Placebo + Sham tDCS
Arm Type
Other
Arm Description
Placebo and Sham Transcranial Direct Current Stimulation
Intervention Type
Drug
Intervention Name(s)
Low-Dose Naltrexone
Other Intervention Name(s)
LDN
Intervention Description
4.5mg daily dose, orally, during 26 days
Intervention Type
Device
Intervention Name(s)
Transcranial Direct Current Stimulation
Other Intervention Name(s)
tDCS
Intervention Description
An anodal electrode was placed on the scalp above the primary motor cortex (M1), contralateral to the dominant cortex. The cathodal electrode was placed on the supraorbital contralateral area. The current used was 2mA during 20 minutes.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
The capsule presented the same format, size and color as LDN capsules, however the excipient used was starch.
Intervention Type
Device
Intervention Name(s)
Sham Transcranial Direct Current Stimulation
Other Intervention Name(s)
Sham tDCS
Intervention Description
Sham-tDCS stimulation consists of an active current during 30 seconds
Primary Outcome Measure Information:
Title
Pain in VAS
Description
Visual Analogue Scale (VAS) that goes from 0 cm (without pain) to 10cm (worst pain).
Time Frame
Change between baseline and after association (26 days from baseline)
Secondary Outcome Measure Information:
Title
Depressive symptoms
Description
Beck Depression Inventory (BDI-II) that goes from 0 (without depressive symptoms) to 63 (worst depressive symptoms)
Time Frame
Change between baseline and after association (26 days from baseline)
Title
Anxiety levels
Description
State-Trait Anxiety Inventory (STAI) divided into state anxiety (from 0 to 52, the higher the worse) and trait anxiety (from 0 to 48, the higher the worse)
Time Frame
Change between baseline and after association (26 days from baseline)
Title
Pain Catastrophizing Thought
Description
Pain Catastrophizing Scale (PCS): divided into rumination (from 0 to 16, the higher the worse), magnification (from 0 to 12, the higher the worse) and hopelessness (from 0 to 24, the higher the worse). Total goes from 0 to 52, the higher the worse
Time Frame
Change between baseline and after association (26 days from baseline)
Title
Profile of Chronic Pain
Description
Profile of Chronic Pain Scale (PCP:S): divided into Frequency and Intensity of Pain (from 0 to 30, the higher the worse), Pain Effect in Activities (from 0 to 36, the higher the worse) and Pain Effect in Emotions (from 0 to 25, the higher the worse)
Time Frame
Change between baseline and after association (26 days from baseline)
Title
Pain Pressure Threshold
Description
Pain Pressure Threshold (PPT) measured using an electronic algometer applied in the right forearm; and patients need to report the first pain sensation (minimum pain) and maximum pain. Threshold goes from 0 to the maximum value the patient can hold, the higher the value, better is the result
Time Frame
Change between baseline and after association (26 days from baseline)
Title
Conditioned Pain Modulation
Description
Conditioned Pain Modulation (CPM) with an algometer (PPT task), the patient informed when felt a pain equal to 6 in the VAS. This pain level was applied in the right forearm for 30 seconds, while the left forearm (non-dominant hand) was submerged in water from 0˚C to 1.5˚C; after 30s, patients reported their pain in each of the arms. CPM = left forearm VAS - 6. (from -4 to 6, the value must be as closest to -4 as possible, meaning the higher the worse)
Time Frame
Change between baseline and after association (26 days from baseline)
Title
Serum BDNF
Description
Blood sample collected and centrifuged, the supernatant aliquoted for BDNF analysis using ELISA technique, according to manufacturer's instructions (values start in 0, patients with fibromyalgia usually have higher levels of serum BDNF, therefore the higher the worse)
Time Frame
Change between baseline and after association (26 days from baseline)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: signed the consent form women from 18 to 65 years confirmed diagnosis of fibromyalgia according 2016 American College of Rheumatology criteria read and write pain higher than 6 in the Visual Analogue Scale (VAS), in the last 3 months chronic stable treatment in the last 3 months. Exclusion Criteria: in use of opioid drugs; pregnancy or not using anticontraceptive history of alcohol or drug abuse in the last 6 months history of neurological pathologies history of arrhythmia history of use of drugs that might change vascular response history of head trauma history of neurosurgery decompensated systemic diseases or chronic inflammatory diseases (lupus, rheumatoid arthritis, Sjogren syndrome, Reiter syndrome) history of non-compensated hypothyroidism personal history of cancer.
Facility Information:
Facility Name
Universidade La Salle
City
Canoas
State/Province
Rio Grande Do Sul
ZIP/Postal Code
92010-000
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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LDN and tDCS in Fibromyalgia

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