CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 487 enrolled
Drug / intervention
conventional DMARD combination +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00764725
NCT00764725Phase 4Completed

A Prospective Randomized, Open, Multi-Center Trial Comparing TNF-Blockade + MTX to MTX+SSZ+HCQ in Patients With Early RA With an Inadequate Response to MTX

Karolinska Institutet·interventional·Posted Oct 2, 2008·Updated Dec 23, 2008

In Brief

A Phase 4 clinical trial evaluating conventional DMARD combination and MTX plus anti-TNF for Rheumatoid Arthritis. Completed, enrolled 487 participants.

Detailed Summary

The Swefot trial was designed to compare two treatment strategies for patients with early rheumatoid arthritis (less than 1 year symptom duration): the use of a combination of traditional antirheumatic medications (DMARDs), versus a combination including a newer "biological" anti-TNF medication. In order to make this trial consistent with current practices in rheumatology, all patients were first given the most commonly used antirheumatic medication, methotrexate (MTX). After 3-4 months those patients who had not responded adequately to this treatment were randomized to receive either MTX plus sulfasalazine plus hydroxychloroquine, or MTX plus infliximab. Again, to be truly life-like, the trial allowed patients who could not tolerate one of the added medications to switch in treatment - but keeping with the same strategy - so that sulfasalazine plus hydroxychloroquine could be replaced by cyclosporin A, and infliximab by etanercept. The primary outcome in this trial was the percentage of patients who, after one year of treatment, achieved a "good response" as defined by Eular.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 4CompletedFinished
2003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 2, 2008
Enrollment StartDec 1, 2002
Primary CompletionApr 1, 2007
Study CompletionDec 1, 2008
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 17.8 years ago

Interventions

conventional DMARD combinationdrug

MTX+SSZ+Plaquenil; can be changed to MTX+cyclosporin within protocol

MTX plus anti-TNFbiological

MTX + infliximab; can be changed to MTX + etanercept within protocol