Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2011 by St. Jude Medical.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by (Responsible Party):
St. Jude Medical
ClinicalTrials.gov Identifier:
NCT01298609
First received: February 14, 2011
Last updated: October 4, 2011
Last verified: October 2011

February 14, 2011
October 4, 2011
June 2010
July 2012   (final data collection date for primary outcome measure)
Fibromyalgia Impact Questionnaire (FIQ) [ Time Frame: End of 6 week stimulation trial ] [ Designated as safety issue: No ]

The Fibromyalgia Impact Questionnaire (FIQ) is a self administered scale that was developed to measure fibromyalgia patient status, progress and outcomes. It measures the components of health that are most affected by fibromyalgia. The maximum score is 100 and a higher score indicates a greater impact of the syndrome on the person.

The change in the Fibromyalgia Impact Questionnaire (FIQ) will be analyzed and reported.

Same as current
Complete list of historical versions of study NCT01298609 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia
A Randomized Controlled Pilot Study to Examine the Efficacy of Greater Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia

The study is designed as a prospective, randomized, double-blind, single center study with a 6 month duration post permanent system implantation. Forty patients will be implanted.

During trial stimulation, patients will be randomized into one of two study arms for two weeks. Crossover will occur at the 2 week study visit to the opposite group. After completion of these two arms, every patient will subsequently complete participation in the third study arm.

After completion of the third arm, patients will be evaluated to determine if they are a positive responder responder. If so, the patient will have the option of obtaining the permanent implant.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Fibromyalgia
Device: Occipital Nerve Stimulation
Stimulation will be performed at various levels in each study arm
  • Active Comparator: Suprathreshold Stimulation
    patients will be stimulated at supra-sensory threshold levels for two weeks
    Intervention: Device: Occipital Nerve Stimulation
  • Sham Comparator: minimal stimulation
    patients will be stimulated at minimal stimulation for two weeks
    Intervention: Device: Occipital Nerve Stimulation
  • Active Comparator: Subthreshold Stimulation
    patients will be stimulated at sub-sensory threshold stimulation for two weeks
    Intervention: Device: Occipital Nerve Stimulation
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
40
August 2012
July 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Patients able to provide informed consent to participate in the study;
  2. Patient has had chronic widespread pain for at least 3 months in all 4 body quadrants;
  3. Patient has at least 11 out of 18 tender points based on the tender points examination;
  4. Patient has attempted "best" medical therapy and has tried and failed at least three documented medically supervised treatments (including, but not limited to drugs, physical therapy, acupuncture, etc.);
  5. Patient medication has remained stable for at least 4 weeks prior to baseline data collection;
  6. Psychological screening has been completed and the patient has been cleared by a psychologist as a suitable study candidate;
  7. Patient agrees not to add or increase medication throughout the randomization trial period of the study;
  8. Patient is willing to cooperate with the study requirements including compliance with the treatment regimen and completion of all office visits.

Exclusion Criteria:

  1. Patient has current evidence of any psychiatric disorder, as documented by the DSM-IV-TR criteria with psychotic characteristics, (e.g. bipolar disorder, major depressive disorder);
  2. Patient has been diagnosed with any disease mimicking the symptoms of the Fibromyalgia Syndrome (e.g. Epstein Barr, autoimmune diseases, etc.) that is not currently being treated or has not been stable for at least 6 months;
  3. Patient is currently in active menopause;
  4. Patient has been diagnosed with sleep apnea and is not currently involved in a treatment regime;
  5. Patient has a history of substance abuse or substance dependency in the past 6 months prior to baseline data collection;
  6. Patient currently participating in another clinical study;
  7. Patient with demand-type cardiac pacemakers, an infusion pump or any implantable neurostimulator device;
  8. Patient is likely to require an MRI evaluation in the future;
  9. Patient is not willing to maintain current medication regimen;
  10. Female candidates of child bearing potential who are pregnant (confirmed by positive urine/blood pregnancy test), not using adequate contraception as determined by the investigator, or nursing (lactating) a child.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Belgium
 
NCT01298609
CRD_545
No
St. Jude Medical
St. Jude Medical
Not Provided
Study Director: Roni Diaz St. Jude Medical
St. Jude Medical
October 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP