Male or female, 18 years of age or older. Ulcerative Colitis described according usual criteria, diagnosed for at least 1 year. Oral maintenance treatment with 5-aminosalicylic acid (5-ASA) only for at least 3 months with a dosage of 2 to 3 g/day. Clinical remission for at least 3 months (Mayo Clinic score) and endoscopic remission (endoscopic score of Mayo Clinic) at the inclusion. Signed informed consent form.
Inclusion Criteria: * Male or female, 18 years of age or older. * Ulcerative colitis described according to usual criteria, diagnosed for at least 1 year. * Oral maintenance treatment with 5-aminosalicylic acid (5-ASA) only for at least 3 months with a dosage of 2 to 3 g/day. * Clinical remission for at least 3 months (Mayo Clinic score) and endoscopic remission (endoscopic score of Mayo Clinic) at inclusion. * Signed informed consent form. Exclusion Criteria: * Patients allergic to aspirin or salicylates derivatives * Patients taking the following treatments during the study will be excluded: corticosteroids (oral or rectal route), use of NSAID or Aspirin, any form of sulfasalazine, mesalazine or 4-ASA. * Patients with known significant hepatic or known function abnormalities and/or creatine clearance ≤ 80 ml/min. * Patients with history or physical examination findings indicative of active alcohol or drug abuse. * Women who are pregnant or nursing. * Patients with a history of disease, including mental/emotional disorder that would interfere with their participation in the study. * Patients who participated in another clinical study in the last 3 months. * Patients who are unable to comply with the requirements of the protocol * Female of childbearing potential without efficacious contraception.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
6
Observe patients with inactive ulcerative colitis
Hôpital Saint Antoine, Service d'hépato-Gastroentérologie
Paris, France
Change between rectal biopsies performed at D1 and D28 of proliferative index
Time frame: Its aim was to study histological modifications after Pentasa was stopped in non-active ulcerative colitis.
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