Omega-3 Fatty Acid Treatment in Multiple Sclerosis

NCT00360906 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2006-08-07

No results posted yet for this study

Summary

Based on previous clinical studies indicating beneficial treatment effects of omega-3 fatty acids in multiple sclerosis, and the increasing evidence of anti-inflammatory effects of omega-3 fatty acids, this study aims to evaluate treatment effects of concentrated omega-3 fatty acids (Triomar™) in MS, both as monotherapy and in combination with standard immunomodulatory therapy defined as interferon-beta 1a (Rebif™).

Conditions

  • Relapsing-Remitting Multiple Sclerosis

Interventions

DRUG

Triomar™ (omega-3 fatty acids)

Sponsors & Collaborators

  • The Multiple Sclerosis National Competence Centre

    collaborator UNKNOWN
  • The Norwegian Multiple sclerosis Society

    collaborator UNKNOWN
  • Pronova BioPharma

    collaborator INDUSTRY
  • Serono Nordic

    collaborator UNKNOWN
  • Amersham Health

    collaborator INDUSTRY
  • Haukeland University Hospital

    lead OTHER

Principal Investigators

  • Kjell-Morten Myhr, MD, PhD · Dep. of Neurology, Haukeland University Hospital

  • Antonie G. Beiske, MD · Dep. of Neurology, Akershus University Hospital

  • Harald Hovdal, MD · Dep. of Neurology, Trondheim University Hospital

  • Rune Midgard, MD, PhD · Dep. of Neurology, Molde Hospital

  • Ingrid K. Bjørnå, MD · Dep. of Neurology, Buskerud Hospital

  • Olaf A. Henriksen, MD · Dep. of Neurology Nordland Hospital

  • Jan Schepel, MD · Dep. of Neurology Haugesund Hospital

  • Randi Eikeland, MD · Dep. of Neurology Arendal Hospital

  • Terje Kristensen, MD · Dep. of Neurology Fredrikstad Hospital

  • Halfdan Kierulf, MD · Dep. of Neurology Rikshospitalet University Hospital

  • Frøydis Dalane, MD · Dep. of Neurology, Telemark Hospital

  • Alla Bru, MD · Dep. of Neurology, Stavanger University Hospital

  • Grethe Kleveland, MD · Dep. of Neurology, Lillehammer Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-12-31
Completion
2008-07-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00360906 on ClinicalTrials.gov