5-ASA Withdrawal
OtherWithdrawal of 5-ASA therapy
NCT Number: NCT03261206
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.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Phase 4
University of Calgary, Calgary, Alberta, Canada
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Withdrawal of 5-ASA therapy
Time frame: 24 months
CD-related complications include either a CD-related or CD treatment-related surgery, hospitalization, or other complication
Time frame: 12 months
CD-related complications include either a CD-related or CD treatment-related surgery, hospitalization, or other complication
Time frame: 12 months
Time frame: 24 months
Time frame: 12 months
Time frame: 24 months
Time frame: 12 months
Other complication excludes surgeries or hospitalizations
Time frame: 24 months
Other complication excludes surgeries or hospitalizations
Time frame: 12 months
Time frame: 24 months
Time frame: up to 24 months
CD-related complications include either a CD-related or CD treatment-related surgery, hospitalization, or other complication
Time frame: 6 months
Disease activity assessed by HBI score
Time frame: 12 months
Disease activity assessed by HBI score
Time frame: 24 months
Disease activity assessed by HBI score
Time frame: Base line and 6 months
Quality of life assessed with the Crohn's and Ulcerative Colitis Questionnaire 32-item
Time frame: Base line and 12 months
Quality of life assessed with the Crohn's and Ulcerative Colitis Questionnaire 32-item
Time frame: Base line and 24 months
Quality of life assessed with the Crohn's and Ulcerative Colitis Questionnaire 32-item
Time frame: Base line and 6 months
Time frame: Base line and 12 months
Time frame: Base line and 24 months
Time frame: Base line and 12 months
Time frame: Base line and 24 months
Time frame: 12 months prior to enrollment and 24 months after enrollment
Estimated drug treatment costs before and after enrollment
Time frame: 12 months prior to enrollment and 24 months after enrollment
Estimated costs before and after enrollment
Alimentiv Inc.
Other
Stopping Aminosalicylate Therapy in Inactive Crohn's Disease (STATIC) Study: A Randomized, Open-label, Non-inferiority Trial
Acronym: STATIC
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.
NCT03574948
Colitis, Colitis, Ulcerative
Bonheiden, Belgium
View Trial DetailsNCT05420233
Crohn Disease, Digestive System Diseases
Liège, Belgium
View Trial DetailsNCT05668013
Colitis, Colitis, Ulcerative
San Diego, California, United States
View Trial DetailsNCT07694609
Colitis, Colitis, Ulcerative
Rome, RM, Italy
View Trial Details