Patient registry for children and adolescents with inflammatory bowel disease
Official title: CEDATA GPGE Patient Registry for Children and Adolescents With IBD
Run by University of Giessen · NCT06606756 · Data updated 2026-11-12
This study collects health information from children and teens with inflammatory bowel disease to help improve treatment and care.
Quick facts
| Study type | Observational |
|---|---|
| Ages | Any age to 18 Years |
| Sex | All |
| Enrollment | 6300 (estimated) |
| Sponsor | University of Giessen Academic / other |
| Locations | 1 site (Giessen) |
| Status | Recruiting |
| Started | September 1, 2004 |
| Main results expected | December 1, 2034 |
| Study ends | December 1, 2034 |
| Registry record updated | September 23, 2024 |
| Trial ID | NCT06606756 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this registry are children and adolescents diagnosed with inflammatory bowel disease.
✕Probably not a fit
Patients without a diagnosis of inflammatory bowel disease will not benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
CEDATA GPGE is an observational study that collects clinical data from children and adolescents diagnosed with inflammatory bowel disease (IBD) across pediatric gastroenterology centers in German-speaking countries. The data is gathered in a pseudonymized manner through an online platform at the onset and during follow-up of the disease. The initiative is coordinated by a leading group of 15 experts in pediatric gastroenterology who meet biannually to enhance research and quality improvement efforts in the field.
Why it matters
Potential benefit: If successful, this registry could improve the understanding and management of inflammatory bowel disease in pediatric patients.
How similar studies have gone: Other patient registries for inflammatory bowel disease have shown success in improving patient outcomes and understanding of the disease.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Inflammatory Bowel Disease Exclusion Criteria: * none
Where it's running
-
University Giessen
Giessen, Germany Recruiting
Study contacts
- Study coordinator: Jan de Laffolie, MD
- Email: jan.delaffolie@paediat.med.uni-giessen.de
- Phone: +49 641 985 43400
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
DISC-0974-201 for adults with IBD-related anemia
This Phase 2 trial will test whether DISC-0974-201 helps adults with inflammatory bowel disease who have anemia driven by inflammation.
-
Moderate breathing and movement: Can regular exercise help people with quiescent inflammatory bowel disease feel better?
This trial tests whether a moderate-intensity exercise program improves quality of life for adults with Crohn's disease or ulcerative colitis who are currently in clinical remission.
-
Mediterranean Diet and Time-Restricted Feeding in Ulcerative Colitis in Remission
This study tests whether a Mediterranean diet, with or without an 8-hour eating window, helps gut health and quality of life in adults with ulcerative colitis in remission.
-
Screening for lipid disorders in children and teens with chronic diseases to flag cardiovascular risk
This study tests a blood test and a questionnaire to screen children and teens with chronic conditions for lipid metabolism disorders and familial hyperlipidemia.
-
Wearable data to spot IBD flareups in people with ulcerative colitis or Crohn's disease
This study tests whether heart‑rate variability from participants’ own wearables can help predict IBD flares.
-
PVT401 in healthy adults
This trial will test intravenous PVT401 in healthy adults who carry the HLA DRB4*0101 or DRB4*0103 allele to see how the drug behaves in the body and whether single and multiple doses are safe.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.