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Effect of pentoxifylline on multiple sclerosis treatment

Investigating the effects of Pentoxifylline on reduction of relapse frequency in patients with relapsing-remitting multiple sclerosis (RRMS)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201301148430N7
Enrollment
44
Registered
2014-02-25
Start date
2012-06-30
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: intervention group : tablet Pentoxifylline 800 mg daily for 2 months. Intervention 2: control group: placebo with similar dose of intervention group.
Treatment - Drugs
intervention group : tablet Pentoxifylline 800 mg daily for 2 months
control group: placebo with similar dose of intervention group

Sponsors

Neuroscience Research center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: new case of MS compatible with MC donalds ?relapsing -remitting pattern ? age between 20-40 Y/O exclusion criteria: other patterns of MS except RRMS? other immunomodulatory medications use except beta interferon?pregnancy and lactation ?concurrent autoimmune diseases and it's related drugs?allergy to drug ?liver disease?renal disease ?antihypertensive and ASA and anticoagolant drugs

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Recurrence. Timepoint: monthly. Method of measurement: clinical examination.;Expanded Disability Status Scale. Timepoint: before of the treatment, 6 months after and at the end of the treatment. Method of measurement: clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactakbar hamzei moghaddam MD

kerman university of medical science

shafahospital@kmu.ac.ir+98 34121157809

Outcome results

None listed

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