The Effect of Milnacipran on Fatigue and Quality of Life in Lupus Patients



Status:Withdrawn
Conditions:Fibromyalgia, Lupus, Pain
Therapuetic Areas:Immunology / Infectious Diseases, Musculoskeletal, Rheumatology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:October 2011
End Date:November 2013

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The Effect of Milnacipran on Fatigue and Quality of Life in a Lupus Cohort

Systemic lupus erythematosus (SLE) is a chronic multi-system autoimmune disease impacting
the physical, social, psychological health and quality of life of patients. Fatigue and pain
are aspects of SLE patients which affect their health related quality of life (HRQOL). The
purpose of this study is to determine the effect of milnacipran on fatigue in SLE patients
with widespread pain (WSP) or fibromyalgia syndrome (FMS). A secondary objective will be to
determine the effect of milnacipran on pain and quality of life measurements. Fifty SLE male
and female patients, 18 years and older, will be recruited for a 15-week study, in which
patients will be receive 14 weeks of milnacipran 50-100 mg twice a day or placebo.
Measurements of fatigue, pain, and HRQOL will be compared between the milnacipran and
placebo groups at the screening visit, baseline visit, week number 6, and week number 14.
Milnacipran has been shown to be an effective treatment for pain, fatigue and physical
function in FMS patients. To date, no clinical trials have demonstrated efficacy for the
treatment of fatigue in SLE patients with concomitant WSP or FMS. The investigators
hypothesize, based on FMS studies, that the milnacipran treated patients will have less
fatigue than those in the placebo group. In addition, compared to control arm, those treated
with the study drug will have less pain and improved quality of life.


Inclusion Criteria:

- Female or male age 18 or older.

- Has fulfilled the 1997 classification criteria for SLE.

- Has chronic WSP or FMS.

- Score a 40 or more on the visual analog score (VAS) for fatigue.

Exclusion Criteria:

- Has a chronic inflammatory autoimmune condition other than SLE.

- Has an acute or uncontrolled co-morbid medical condition.

- Uncontrolled narrow angle glaucoma.

- Has been hospitalized in the last four months for a lupus flare.

- Pregnant or breast feeding.

- Has a current or prior major depressive disorder or other DSM IV diagnosis within 2
years of the screening visit.

- The use of antidepressants, MAO inhibitors, antipsychotics or lithium

- The use of pregabalin or milnacipran within 2-4 weeks.

- Has received cyclophosphamide and or rituximab within 4 and 6 months.

- Unable to speak, read, and understand English.
We found this trial at
2
sites
11234 Anderson St
Loma Linda, California 92354
(909) 558-4000
Loma Linda University Medical Center An outgrowth of the original Sanitarium on the hill in...
?
mi
from
Loma Linda, CA
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11234 Anderson St
Loma Linda, California 92354
(909) 558-4000
Loma Linda University Medical Center An outgrowth of the original Sanitarium on the hill in...
?
mi
from
Loma Linda, CA
Click here to add this to my saved trials