Crohn's Disease Clinical Trial
OBJECTIVES:
I. Assess the efficacy and safety of 4-aminosalicylic acid in patients with active Crohn's
disease of the small bowel.
PROTOCOL OUTLINE: This is a randomized, placebo controlled, multicenter study. Patients are
randomized to receive either oral 4-aminosalicylic acid (4-ASA) or placebo twice a day for
12 weeks. After 12 weeks patients who improved with 4-ASA and those who received placebo are
given the option of receiving 4-ASA for an additional year.
Patients who were randomized to receive 4-ASA and continue treatment after 12 weeks are
followed every 3 months for 1 year. Patients who were randomized to receive placebo and
begin 4-ASA therapy after 12 weeks are followed monthly for 3 months, then every 3 months
for 1 year.
Completion date provided represents the completion date of the grant per OOPD records
;
Allocation: Randomized, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Active, not recruiting |
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