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Effectiveness of simvastatin on multiple sclerosis (MS)

Effectiveness of simvastatin on improvement of multiple sclerosis (MS).

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015112925284N1
Enrollment
60
Registered
2015-12-06
Start date
2016-01-21
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. Multiple sclerosis

Interventions

Intervention 1: Control group: Received 30 µg interferon beta-1a
intra-muscular injection
for 6-months. Intervention 2: Intervention group: Received 30 µg interferon beta-1a with 40 mg atorvastatin
for 6-months.
Treatment - Drugs
Control group: Received 30 µg interferon beta-1a
for 6-months
Intervention group: Received 30 µg interferon beta-1a with 40 mg atorvastatin

Sponsors

Vice Chancellor for Research, Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Relapsing-remitting MS patients; at least 1 relapse in the previous 12 months; more than three lesions on spinal or brain magnetic resonance imaging or both; baseline expanded disability status scale (EDSS) from 0 to 3.5; aged 18–60 years. Exclusion criteria: clinical CIS syndrome, progressive MS, MS patients with acute clinical relapses occurring during the study, drug abuse, renal failure, pregnancy, hepatitis diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Assay of cell amplification of peripheral blood luokocytes. Timepoint: 6 months after entering the intervention. Method of measurement: MTT assay.

Secondary

MeasureTime frame
Level of cytokines. Timepoint: 6 months after entering the intervention. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFardin Faraji

Arak University of Medical Sciences

ghazaviali@yahoo.com+98 86 3313 6058

Outcome results

None listed

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