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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03256266
Other study ID # intestinal organoids
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2017
Est. completion date July 2023

Study information

Verified date January 2023
Source University of Erlangen-Nürnberg Medical School
Contact Yurdagül Zopf, Prof
Phone 49 9131 8545218
Email yurdaguel.zopf@uk-erlangen.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study evaluates the effect of nutrient antigens or therapeutic agents on human small intestinal organoids.


Description:

Small intestinal biopsies will be taken to establish human intestinal organoids in vitro. The organoids will be propagated and various antigens will be checked for their effects on proliferation, production of inflammatory components or signal cascade.


Recruitment information / eligibility

Status Recruiting
Enrollment 375
Est. completion date July 2023
Est. primary completion date July 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients with gastrointestinal disorders and therapeutical indication of gastroduodenoscopy or coloscopy - healthy controls for preventive medical check-up Exclusion Criteria: - pregnant women

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Department of Medicine 1, Hector Center for Nutrition, Exercise and Sports, Friedrich-Alexander-University Erlangen-Nuremberg Erlangen

Sponsors (1)

Lead Sponsor Collaborator
University of Erlangen-Nürnberg Medical School

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Determination of proliferation, apoptosis, histology, and cytokine Expression before and after Antigen provocation of organoids with gluten peptides, nutritional Antigens, GLP-antagonist, or TNF antagonists Determination of effects on organoids after antigen Stimulation with ELISA, histochemistry, RNA or proteome analysis baseline vs 24h vs 48h vs 72h