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Evaluation the effect of adding methylprednisolone to mitoxantrone on progressive multiple sclerosis treatment

Evaluation the effect of Mitoxantrone and Mitoxantrone plus Methylprednisolone on Progressive Multiple Sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201107145943N3
Enrollment
70
Registered
2011-07-22
Start date
2010-03-21
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. Demyelinating diseases of the central nervous system

Interventions

Intervention 1: Control group: mitoxantrone 20 mg as well as methylprednisolone 500 mg monthly for 6 consecutive months. Intervention 2: Intervention group: mitoxantrone 20 mg monthly for 6 consecutiv
Treatment - Drugs
Control group: mitoxantrone 20 mg as well as methylprednisolone 500 mg monthly for 6 consecutive months
Intervention group: mitoxantrone 20 mg monthly for 6 consecutive months

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: presence of progressive MS, age between 20 to 50 Exclusion criteria: Age below 20 or above 50, Immune deficiency, cancer, Pregnancy or breast feeding, Renal or heart failure, Leukopenia during the injection (the reduction of neutrophils to less than 1500/ml), having received corticosteroids within 6 months before the trial

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
MRI plaque numbers. Timepoint: 6 months and 1 year after the intervention. Method of measurement: Based on MRI imaging.;Expanded Disability Status Scale (EDSS). Timepoint: 6 months and 1 year after the intervention. Method of measurement: Based on definit idex.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Mellat Ardekani

Yazd Univesity of Medical Sciences

Ali_mellat@ssu.ac.ir+98 35 1822 4001

Outcome results

None listed

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