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OpenTrials
Completed

NCT Number: NCT00554710

Top Down Versus Step Up Strategies in Crohn's Disease

The study prospectively compares two treatment algorithms for newly diagnosed Crohn's disease: one 'aggressive' treatment with early introduction of immunomodulators and biologicals and one 'standard treatment' with corticosteroids and only later introduction of immunosuppressives and biologicals if disease activity requires that.

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Key information

Age range

16 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Imelda GI Clinical Research Center

Bonheiden, 2820, Belgium

About this study

This two year open-label randomized trial compares the early use of combined immunosuppression to conventional management in patients with active Crohn's disease who have not previously received glucocorticoids, antimetabolites, or infliximab. Patients assigned to combined immunosuppression receive azathioprine and 3 infusions of 5 milligrams per kilogram of body weight of infliximab at weeks 0, 2, and 6. Retreatment with infliximab and, if ultimately necessary, corticosteroids are used to control disease activity. Patients assigned to conventional management receive corticosteroids followed, in sequence, by azathioprine and infliximab. The primary outcome measure is remission without corticosteroids and without bowel resection at weeks 26 and 52.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age 16 - 75 years
  • diagnosis of Crohn's disease within the past 4 years
  • no previous treatment with corticosteroids, antimetabolites, or biologic agents.
  • Active Crohn's disease, defined by a Crohn's Disease Activity Index (CDAI)20 score of greater than 200 points for a minimum of 2 weeks prior to randomization.

Exclusion criteria

  • immediate need for surgery
  • symptomatic stenosis or ileal/colonic strictures with prestenotic dilatation;
  • signs, symptoms or laboratory tests indicating severe, medical disease;
  • documented chronic infection
  • a positive stool culture for pathogens
  • a positive tuberculin test or a chest radiograph consistent with tuberculosis.
  • malignancy
  • allergy to murine proteins
  • pregnancy
  • substance abuse

Treatment and study plan

infliximab+azathioprine

Drug

infliximab 5 mg/kg at week 0,2 and 6 + azathioprine 2-2.5 mg/kg

Other names: remicade/imuran

methylprednisolone or budesonide

Drug

methylprednisolone 32 mg followed by taper or budesonide 9 mg/day followed by taper

Other names: Medrol, entocort, budenofalk

Primary outcomes

  1. remission without corticosteroids and without surgical resection

    Time frame: month 6 and 12 after inclusion

Secondary outcomes

  1. the time to relapse after successful induction therapy

    Time frame: within 24 months

  2. the proportion of patients receiving infliximab, methylprednisolone and antimetabolites

    Time frame: within 24 months

  3. the median serum C-reactive protein concentration

    Time frame: 24 months

  4. the proportion of patients experiencing adverse events

    Time frame: 24 months

  5. the mean endoscopic severity scores and the proportion of patients without ulcers

    Time frame: after 24 months

Sponsors and collaborators

Lead sponsor

Belgian Inflammatory Bowel Disease Research and Development (BIRD) VZW

Other

Collaborators

  • Centocor BV
  • Schering-Plough

Registry information

Official study title

The Ideal Management of Crohn's Disease: Top Down Versus Step Up Strategies. A Prospective Controlled Trial in the Benelux

Important dates

Study start
2001
Study completion
2004
First posted
Nov 7, 2007
Registry last updated
Nov 7, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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