Confocal Laser Endomicroscopy Findings in Patients With Proctosigmoiditis Before and After Initiation of Treatment
Colitis, Ulcerative
About this trial
This is an interventional diagnostic trial for Colitis, Ulcerative focused on measuring confocal laser endomicroscopy, inflammatory bowel disease, colitis, ulcerative
Eligibility Criteria
Inclusion Criteria:
Patients with active proctitis or proctosigmoiditis due to ulcerative colitis, where an indication for treatment and colonoscopy exists. Newly diagnosed as well as patients already in oral 5-ASA therapy, may be included.
The control group will consist of patients without known or suspected IBD. Patients must be of legal age. Patients who have received written informed consent.
Exclusion Criteria:
Increased p-creatinine and/or demonstrated allergy to fluorescein. Pregnant and lactating women. Ongoing systemic immunosuppressive therapy with prednisolone, azathioprine or biological agents.
Sites / Locations
- John Gásdal Karstensen
- Gastroenheden, Herlev Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
colitis, ulcerative
Control group
Enrolled patients will be examined by conventional colonoscopy and confocal laser endomicroscopy before and after initiation of topical treatment, respectively.
A control group will be examined by conventional colonoscopy and confocal laser endomicroscopy.