Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT03261206

Stopping Aminosalicylate Therapy in Inactive Crohn's Disease

The purpose of this study is to assess whether withdrawal of aminosalicylate (5-ASA) is non-inferior to continuation of 5-ASA therapy in Crohn's disease (CD) subjects in remission.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Calgary, Calgary, Alberta, Canada

Loading trial locations.

About this study

Aminosalicylate (5-ASA) agents have proven effective for inducing and maintaining remission in mild to moderate ulcerative colitis (UC) and thus are commonly used as first-line agents for patients with Crohn's disease (CD) in remission. However, there is uncertainty regarding their effectiveness for CD.

In this open-label, randomized study, participants with CD in remission will be allocated to either continue their 5-ASA therapy or withdraw their 5-ASA. The purpose is to investigate if withdrawal of 5-ASA therapy is not unacceptably less effective than continuing on 5-ASA in maintaining CD remission over a 24 month period.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Documented diagnosis of CD at least 3 months prior to enrollment
  • Taking any brand or dosage of an oral aminosalicylate for at least 6 months
  • Subject-confirmed compliance with current aminosalicylate therapy (taking at least 75% of prescribed doses)
  • CD currently in clinical remission
  • Able to participate fully in all aspects of the clinical trial
  • Written informed consent obtained and documented

Exclusion criteria

  • A current diagnosis of UC, indeterminate colitis, microscopic colitis, or diverticular disease-associated colitis
  • A diagnosis of short-bowel syndrome
  • Active perianal disease
  • Active fistulizing disease
  • A flare of CD within 3 months prior to enrollment requiring initiation/escalation of medical therapy or surgery
  • Use of systemic corticosteroids for CD (2 continuous weeks or more) within 3 months prior to enrollment
  • Any major resective bowel surgery for CD (ileal resection, ileocecal resection, proctocolectomy, colectomy, enterectomy, ostomy formation and repair, anastomosis/reanastomosis) within 6 months prior to enrollment
  • Unwillingness to stop taking aminosalicylates for the duration of the trial
  • Untreated bile salt malabsorption that, in the opinion of the investigator, may interfere with accurate study HBI assessment
  • Serious underlying disease other than CD that, in the opinion of the investigator, may interfere with the subject's ability to participate fully in the study
  • History of active alcohol or drug abuse that, in the opinion of the investigator, may interfere with the subject's ability to comply with the study procedures
  • Currently participating in another interventional trial, or previous participation within the last 3 months

Treatment and study plan

5-ASA Withdrawal

Other

Withdrawal of 5-ASA therapy

Primary outcomes

  1. CD-related complications at 2 years

    Time frame: 24 months

    CD-related complications include either a CD-related or CD treatment-related surgery, hospitalization, or other complication

Secondary outcomes

  1. CD-related complications at 1 year

    Time frame: 12 months

    CD-related complications include either a CD-related or CD treatment-related surgery, hospitalization, or other complication

  2. CD-related or CD-treatment related surgeries at 1 year

    Time frame: 12 months

  3. CD-related or CD-treatment related surgeries at 2 years

    Time frame: 24 months

  4. CD-related or CD-treatment related hospitalizations at 1 year

    Time frame: 12 months

  5. CD-related or CD-treatment related hospitalizations at 2 years

    Time frame: 24 months

  6. Other CD-related or CD-treatment related complications at 1 year

    Time frame: 12 months

    Other complication excludes surgeries or hospitalizations

  7. Other CD-related or CD-treatment related complications at 2 years

    Time frame: 24 months

    Other complication excludes surgeries or hospitalizations

  8. Proportion of patients who require the use of systemic corticosteroids for treatment of CD flares at 1 year

    Time frame: 12 months

  9. Proportion of patients who require the use of systemic corticosteroids for treatment of CD flares at 2 years

    Time frame: 24 months

  10. Time to first CD-related complication

    Time frame: up to 24 months

    CD-related complications include either a CD-related or CD treatment-related surgery, hospitalization, or other complication

  11. Change in disease activity at 6 months

    Time frame: 6 months

    Disease activity assessed by HBI score

  12. Change in disease activity at 12 months

    Time frame: 12 months

    Disease activity assessed by HBI score

  13. Change in disease activity at 24 months

    Time frame: 24 months

    Disease activity assessed by HBI score

  14. Change in self-assessed quality of life at 6 months

    Time frame: Base line and 6 months

    Quality of life assessed with the Crohn's and Ulcerative Colitis Questionnaire 32-item

  15. Change in self-assessed quality of life at 1 year

    Time frame: Base line and 12 months

    Quality of life assessed with the Crohn's and Ulcerative Colitis Questionnaire 32-item

  16. Change in self-assessed quality of life at 2 years

    Time frame: Base line and 24 months

    Quality of life assessed with the Crohn's and Ulcerative Colitis Questionnaire 32-item

  17. Change in C-reactive protein concentration at 6 months

    Time frame: Base line and 6 months

  18. Change in C-reactive protein concentration at 1 year

    Time frame: Base line and 12 months

  19. Change in C-reactive protein concentration at 2 years

    Time frame: Base line and 24 months

  20. Change in fecal calprotectin concentration at 1 year

    Time frame: Base line and 12 months

  21. Change in fecal calprotectin concentration at 2 years

    Time frame: Base line and 24 months

  22. Change in CD-related drug treatment costs at 2 years

    Time frame: 12 months prior to enrollment and 24 months after enrollment

    Estimated drug treatment costs before and after enrollment

  23. Change in CD-related and total healthcare costs at 2 years

    Time frame: 12 months prior to enrollment and 24 months after enrollment

    Estimated costs before and after enrollment

Sponsors and collaborators

Lead sponsor

Alimentiv Inc.

Other

Collaborators

  • Academic Medical Organization of Southwestern Ontario

Registry information

Official study title

Stopping Aminosalicylate Therapy in Inactive Crohn's Disease (STATIC) Study: A Randomized, Open-label, Non-inferiority Trial

Acronym: STATIC

Important dates

Study start
2017
Primary completion
2026
Study completion
2026
First posted
Aug 24, 2017
Registry last updated
May 28, 2026

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.

Published trials that share one or more normalized conditions with this study.