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A randomised trial of aminosalicylate withdrawal in patients with ulcerative colitis in established remission on combination treatment of azathioprine (or 6-mercaptopurine) and an aminosalicylate - CASA trial

Phase 1
Conditions
The medical condition is Ulcerative Colitis.
Registration Number
EUCTR2005-000695-40-GB
Lead Sponsor
niversity of Nottingham
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Not specified
Target Recruitment
420
Inclusion Criteria

1) Male and female patients aged between 18 and 75 years with ulcerative colitis.

2) Patients whose ulcerative colitis has been in clinical remission, defined as, being off steroids for 3 months or longer.

3) Patients taking both azathioprine (or 6 mercaptopurine) and an aminosalicylate.

4) Patients taking azathioprine (>50mg/day) OR 6-mercaptopurine (>25mg/day) at a stable dose for at least 8 weeks.

5) Patients taking an aminosalicylate at a stable dose (specified below) for at least 4 weeks: sulphasalazine >1.5g/day, Pentasa (slow release mesalazine) >750mg/day, Asacol (mesalazine)or generic equivalents >800mg/day, Colazide (balsalazide) >2.25g/day, Dipentum (olsalazine) >750mg/day

6) Patients on combined treatment with azathioprine (or 6-MP) and an aminosalicylate for a minimum of 6 months but no more than 4 years. Patients may enter if they have briefly been off either treatment during this time (eg because of abnormal blood test results) but prescription of each drug should cover at least 85% of the period of time for continuous drug treatment to be declared. NB Duration of aminosalicylate may be longer.

7) Patients who have given written informed consent.

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1) Patients with Crohn’s disease.

2) Patients with a baseline Walmsley Simple Activity Index >2.

3) Patients with a baseline sigmoidoscopy grade of >2 (Baron Scale).

4) Patients requiring long term treatment with oral steroids for any medical condition.

5) Women who are pregnant or lactating.

6) Patients with known HIV infection.

7) Other serious medical or psychiatric illness currently ongoing, or experienced within the past three months, that in the opinion of the investigator would compromise the study.

8) Patients unable to comply with the protocol requirements, including severe alcohol and drug misuse or abuse

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: This study will help define the medical management for patients with difficult ulcerative colitis who have achieved remission on azathioprine (or 6-mercaptopurine) and on an aminosalicylate. It is important to determine whether, after the introduction of azathioprine with remission established, there is any extra benefit in continuing the aminosalicylate treatment;Secondary Objective: To identify factors predictive of the success of the different maintenance treatment regimes;Primary end point(s): Relapse of colitis, defined by symptoms and sigmoidoscopy findings.
Secondary Outcome Measures
NameTimeMethod
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