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Follow-up Study With Retarded Release Phosphatidylcholine in Ulcerative Colitis

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clinicaltrials.gov/study/NCT00463619
Is a
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Clinical study
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Clinical Study attributes

NCT Number
NCT004636190
Health Conditions in Trial
Ulcerative colitis
Ulcerative colitis
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Trial Recruitment Size
1320
Trial Sponsor
Heidelberg University
Heidelberg University
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Clinical Trial Start Date
2000
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Primary Completion Date
2010
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Study Completion Date
2010
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Clinical Trial Study Type
Observational0
Observational Clinical Trial Type
Cohort0
Observational Study Perspective
Prospective0
Last Updated
August 16, 2011
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Study summary

Follow-Up Study with Retarded Release Phosphatidylcholine in Ulcerative Colitis Objectives: The objective of the study is to evaluate the follow up of patients treated with retarded release phosphatidylcholine in three controlled, randomized studies. Main question is to investigate whether treatment with phosphatidylcholine could spare patients the intake of steroids and immunosuppressants without clinical deterioration. Study population: * Retarded release phosphatidylcholine in chronic-active ulcerative colitis. * Retarded release phosphatidylcholine in steroid dependent ulcerative colitis. * Dose finding study for retarded release phosphatidylcholine Outcome parameters: Definition of remission: 1. SCCAI \<2,5 2. Likert scale: grade 1 or 2 3. subjective impression of remission: yes/no 4. no blood in stool Definition of relapse: 1. subjective impression: yes/no 2. SCCAI ≥ 5 3. blood in stool Definition of low clinical activity: SCCAI \< 5 Primary endpoint: sparing effect of steroids and/or immunosuppressants by rPC in chronic active UC. Secondary endpoints 1. maintenance of continuous remission 2. improvement of disease activity: a. clinical activity (SCCAI) b.life quality (SIBDQ-D) c.Likert Score 3. relapse rate: a. time to first relapse b. clinical activity during relapses c. number of relapses in relation to length of treatment

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