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Newer Antidepressants in Combination With Pregabalin for Fibromyalgia Syndrome

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Amitriptyline
Venlafaxine
Paroxetine
Sponsored by
Mansoura University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring Pregabalin, Fibromyalgia

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Fibromyalgia
  • Receiving pregabalin daily

Exclusion Criteria:

  • Pathologies mimicking the symptoms of fibromyalgia
  • Acute systemic inflammatory diseases
  • Infections
  • Pregnancy
  • Lactating

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Other

    Active Comparator

    Active Comparator

    Arm Label

    Amitriptyline

    Venlafaxine

    Paroxetine

    Arm Description

    Amitriptyline 25 mg/day

    Venlafaxine 75 mg/day

    Paroxetine 25 mg/day

    Outcomes

    Primary Outcome Measures

    Somatic Symptoms Scale-8 (SSS-8)
    Using the 8-points Somatic Symptoms Score

    Secondary Outcome Measures

    Center for Epidemiological Studies Depression (CSED)
    According to the Center for Epidemiological Studies Depression (CSED) questionnaire
    Life satisfaction
    Using a life satisfaction score
    Mood
    Using a mood score
    Sleep quality
    Using a sleep quality questionnaire
    Fatigue
    Using a fatigue questionnaire
    Tolerability
    Using a tolerability questionnaire

    Full Information

    First Posted
    May 16, 2015
    Last Updated
    May 21, 2015
    Sponsor
    Mansoura University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02451475
    Brief Title
    Newer Antidepressants in Combination With Pregabalin for Fibromyalgia Syndrome
    Official Title
    Comparative Effectiveness of Newer Antidepressants in Combination With Pregabalin for Fibromyalgia Syndrome: A Controlled Randomized Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    February 2013 (undefined)
    Primary Completion Date
    September 2014 (Actual)
    Study Completion Date
    October 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Mansoura University

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Background: The investigator hypothesized that the combined use of pregabalin and paroxetine would be associated with comparable Somatic Symptoms Scale-8 (SSS-8) and higher tolerability than amitriptyline or venlafaxine. Methods: After ethical approval, 75 patients with diagnosed fibromyalgia who were receiving pregabalin 75 mg/day, were randomly allocated to receive amitriptyline 25 mg/day (n = 24), venlafaxine 75 mg/day (n = 25), or paroxetine 25 mg/day (n = 26). All patients were assessed bi-monthly for consequent six months for the changes in the SSS-8, Center for Epidemiological Studies Depression Scale (CESDS), life satisfaction, mood, sleep quality, fatigue and medication tolerability and adverse effects.
    Detailed Description
    Fibromyalgia is a common cause of chronic widespread disabling pain affecting 2-5% of the young to middle-aged women in developed countries. The American College of Rheumatology has been established new diagnostic criteria for fibromyalgia in 2010 included a widespread pain index (WPI) and categorical scales for cognitive symptoms, unrefreshed sleep, fatigue, and number of somatic symptoms. The definite pathophysiology of chronic pain in fibromyalgia remains unclear. Fibromyalgia is usually associated with depression, anxiety, and alexithymia increasing over age which contribute significantly to reduced patient wellbeing. These may be due to alterations of central pain pathways, hyporeactivity of the hypothalamus-pituitary-adrenal axis, and disturbances in the dopaminergic and serotonergic systems. Thus the European League Against Rheumatism (EULAR) recommends the use of serotonin and noradrenaline reuptake inhibitors (SNRIs) for the treatment of fibromyalgia, to reduce pain and improve function. However, few patients achieve satisfactory pain relief with the sole use of SNRIs. A recent Cochrane review demonstrated only modest improvement in relieving pain without reducing of sleep disturbances, fatigue, or the poor quality of life with the use of duloxetine and milnacipran than placebo in patients with fibromyalgia. More patients experienced adverse events like as nausea, dry mouth, constipation, headache, somnolence, dizziness and insomnia leading to stopping medications. Whereas, the evidence from clinical studies shows that combined use of pregabalin and SNRIs such as duloxetine has potential efficacy and better tolerability during the treatment of improvement of pain, fatigue, and sleep disorders in patients with fibromyalgia. The use of the second-generation antidepressants like as paroxetine (a selective serotonin reuptake inhibitors (SSRIs)) and venlafaxine (SNRIs) may be associated with more tolerability and reduce pain in patients with major depressive disorder. To the best of the investigator's knowledge, the comparison of the long-term efficacy, tolerability, and safety of the combined use of pregabalin with one of the three antidepressants, namely, amitriptyline, venlafaxine, or paroxetine for the treatment of fibromyalgia has not yet been studied. The investigators hypothesized that the combined use of pregabalin and paroxetine would be associated with comparable Somatic Symptoms Scale-8 (SSS-8) and Center for Epidemiological Studies Depression scales (CESD) and higher tolerability than the use of pregabalin with either amitriptyline or venlafaxine.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fibromyalgia
    Keywords
    Pregabalin, Fibromyalgia

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1, Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    75 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Amitriptyline
    Arm Type
    Other
    Arm Description
    Amitriptyline 25 mg/day
    Arm Title
    Venlafaxine
    Arm Type
    Active Comparator
    Arm Description
    Venlafaxine 75 mg/day
    Arm Title
    Paroxetine
    Arm Type
    Active Comparator
    Arm Description
    Paroxetine 25 mg/day
    Intervention Type
    Drug
    Intervention Name(s)
    Amitriptyline
    Intervention Description
    Amitriptyline 25 mg/day
    Intervention Type
    Drug
    Intervention Name(s)
    Venlafaxine
    Intervention Description
    Venlafaxine 75 mg/day
    Intervention Type
    Drug
    Intervention Name(s)
    Paroxetine
    Intervention Description
    Paroxetine 25 mg/day
    Primary Outcome Measure Information:
    Title
    Somatic Symptoms Scale-8 (SSS-8)
    Description
    Using the 8-points Somatic Symptoms Score
    Time Frame
    for six months after start of the medication
    Secondary Outcome Measure Information:
    Title
    Center for Epidemiological Studies Depression (CSED)
    Description
    According to the Center for Epidemiological Studies Depression (CSED) questionnaire
    Time Frame
    for six months after start of the medication
    Title
    Life satisfaction
    Description
    Using a life satisfaction score
    Time Frame
    for six months after start of the medication
    Title
    Mood
    Description
    Using a mood score
    Time Frame
    for six months after start of the medication
    Title
    Sleep quality
    Description
    Using a sleep quality questionnaire
    Time Frame
    for six months after start of the medication
    Title
    Fatigue
    Description
    Using a fatigue questionnaire
    Time Frame
    for six months after start of the medication
    Title
    Tolerability
    Description
    Using a tolerability questionnaire
    Time Frame
    for six months after start of the medication

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Fibromyalgia Receiving pregabalin daily Exclusion Criteria: Pathologies mimicking the symptoms of fibromyalgia Acute systemic inflammatory diseases Infections Pregnancy Lactating
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Eiad Ramzy, MD
    Organizational Affiliation
    Lecturer of Anesthesia and Surgical ICU, Mansoura University , Mansoura City, Egypt
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Newer Antidepressants in Combination With Pregabalin for Fibromyalgia Syndrome

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