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Thiopurines with Low Dose Allopurinol: a prospective one way cross-over study

Completed
Conditions
Crohn
inflammatory bowel disease
10017969
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
NameTimeMethod
<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
NameTimeMethod
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