Thiopurines with Low Dose Allopurinol: a prospective one way cross-over study
Completed
- Conditions
- Crohninflammatory bowel disease10017969
- Registration Number
- NL-OMON42907
- Lead Sponsor
- Meander Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 22
Inclusion Criteria
-Crohn's disease or Colitis Ulcerosa
-At least one month perior usage of 100 mg allopurinol daily with azathioprine or mercaptopurine
-Stable response and adequate concentrations on combination therapy with a thiopurine and allopurinol
-No recent (<1 month) changes in thiopurine dosage
-At least 18 years old
Exclusion Criteria
-Age below 18 years old
-Pregnancy
-Hypersensitivity to azathioprine, mercaptopurine and/or allopurinol
-Severe anemia, leukopenia or thrombocytopenia
-Lesch-Nyhan syndrome
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- 6-TGN and 6-MMP concentrations<br /><br>These are the metabolites of the thiopurine that is being used by a patient.<br /><br>The concentrations before and after the intervention will be measured with (a<br /><br>validated) UPLC-analysis.</p><br>
- Secondary Outcome Measures
Name Time Method