The goal of this observational pilot study with invasive measurements is to explore whether an ingestible sensor pill can be of use in diagnosis or monitoring of disease in patients with ulcerative colitis or colorectal cancer. The main questions it aims to answer are: * which changes in bowel environment can the sensor pill measure in ulcerative colitis and colorectal cancer before and after treatment? * how practical, effective and user-friendly is the sensor pill for measuring bowel environment in patients with bowel disease? Participants will: * take one sensor pill before treatment and take one sensor pill three months after (start of) treatment; * monitor sensor pill bowel exit using a small wearable device; * answer a questionnaire on experience with the sensor pill; * receive an extra bowel ultrasound (non-endoscopic) three months after start of treatment (only for participants with ulcerative colitis).
Age range
18 Years
Sex
ALL
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Intestinal ORP measurements
Timeframe: Baseline and at 3 months after start of treatment.
Disease activity (SCCAI)
Timeframe: Baseline and 3 months after start of treatment.
Disease activity (FC)
Timeframe: Baseline and at 3 months after treatment start.
Tumor stage
Timeframe: Directly after surgical resection
Tumor size
Timeframe: Directly after surgical resection
Tumor resection margin status
Timeframe: Directly after surgical resection
Tumor differentiation grade
Timeframe: Directly after surgical resection
Lotte R Hazeleger, Master of Science