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fluoxetine AND Multiple sclerosis

The Effect of Fluxetine on Fatigue,sleep quality and depression in Patients with Multiple Sclerosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014062017811N3
Enrollment
60
Registered
2014-06-22
Start date
2013-07-02
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis. Demyelinating diseases of the central nervous system

Interventions

Sponsors

Arak University of Medical Science,Office of Vice Chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: age 18–50 years? ?clinically definitive relapsing remitting MS((according to the 2005 revised McDonald criteria)confirmed by a neurologist ? Additional inclusion criteria were an Expanded disability Status Score (EDSS) of less or equal to 5.5 ? exclusion criteria: progressive forms of multiple sclerosis ? an onset of relapse or receipt of any glucocorticoid treatment during trial period ? use of immunomodulatory, immunosuppressive, IVIg or plasmapherasis or antidepressant drugs in the previous 6 months? the use of corticosteroids in the previous 8 weeks ? depression defined as a score of 19 or higher on Beck’s Depression Inventory II ?contraindication to MRI ? other neurological or systemic disorder that would interfere with the assessments ? pregnancy or unwillingness to use acceptable birth control. severe suicidality including ideation, plan, and intentclinically significant ? unstable medical or surgical conditions that would preclude safe and complete participation in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fatigue. Timepoint: week 0 and 24. Method of measurement: FSS(fatigue severity scale) test.;Sleep quality. Timepoint: week 0 and 24. Method of measurement: PSQI test.;Depression. Timepoint: week 0 and 24. Method of measurement: BDI(BECK depression inventory).

Secondary

MeasureTime frame
Clinical status. Timepoint: week 0 and 24. Method of measurement: EDSS (Expanded Disability Status Scale).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShayan Amjadi

Students Research Committe , Medicine faculty , Aarak University of Medical Science

sh.amjadi@arakmu.ac.ir+98 86 3417 3502

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026