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
About this trial
This is an interventional treatment trial for Fibromyalgia focused on measuring Pregabalin, Fibromyalgia
Eligibility Criteria
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
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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