Ulcerative colitis (UC) patients treated with Carotegrast methyl from May 2022 to December 2022
Conditions
Interventions
None listed
Sponsors
Ohmori Toshihide gastro-intestinal Clinic
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients with inadequate response or intolerance to treatment with 5-ASA 2) Patients with moderately active UC (any disease type)
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endoscopic remission rate (Mayo endoscopy score 0, 1 defined as remission) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Incidence of side effects - duration of a drug administration - Endoscopic Image Evaluation - Changes in Mayo Scores - Changes in CAI Scores - Changes in frequency of defecation, diarrhea, presence of bloody stools, and abdominal pain - Comparison of background information between cases that achieved remission and those that did not (cases of remission achieved) - Use of Remission Maintenance Therapy Medications, Relapse or Not, Time to Relapse, Medications and Their Efficacy at Relapse, and Transition Rate to Advanced Therapy (Non-achievers in remission) - Therapy and its efficacy after administration of Carotegrast methyl | — |
Countries
Japan
Contacts
Public ContactToshihide Ohmori
Ohmori Toshihide gastro-intestinal Clinic director
Outcome results
None listed