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A Diagnostic Accuracy Study Testing Fecal Biomarkers In Comparison To Endoscopic Examination

Diagnostische Genauigkeit fäkaler Biomarker im Vergleich Zur Endoskopie Mit Und Ohne Konfokaler Laserendomikroskopie in Der Routineversorgung Zur Bestimmung Der Entzündungsaktivität Bei Patienten Mit Gastrointestinalen Diagnosen

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04849936
Enrollment
300
Registered
2021-04-19
Start date
2020-07-13
Completion date
2023-08-31
Last updated
2022-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory Bowel Diseases

Keywords

inflammatory bowel diseases, fecal biomarkers, calprotectin, lactoferrin, pmn-elastase, human beta-defensin, zonulin

Brief summary

In this study it will be explored whether the levels of fecal biomarkers are associated with histologic inflammation of the intestinal mucosa and concomitant alteration of the mucosal permeability. The aim of the study is to assess the diagnostic accuracy of fecal biomarkers especially to detect the potential of differentiation between inflammatory and functional gastrointestinal diseases. The following biomarkers will be examined in the stool of the participants: calprotectin, lactoferrin, pmn-elastase, human beta-defensin, zonulin, alpha-antitrypsin.

Detailed description

For this study inpatients and outpatients of the clinic for integrative medicine and naturopathy Bamberg, Germany, who had a routine gastroscopy and/or coloscopy with tissue biopsy or an endoscopy with confocal laser endomicroscopy and tissue biopsy were enclosed. These patients, who were examined during a routine diagnostics, should submit an extra morning stool sample up to two weeks before or after the gastroscopy and/or coloscopy to generate the data of the fecal biomarker mentioned above. On the basis of the biopsy samples generated through the routine examination we can determine the histology scores, Nancy Index and Riley Score. The determined scores, the data of the fecal biomarkers and the results of the confocal laser endomicroscopy as well as, if available, more clinical data such as the clinical activity index (CAI), the MAYO-Score/Disease Activity Index (DAI), the endoscopic Rachmilewitz-Index (REI) and the Questionnaire for inflammatory bowel disease (IBDQ) will be anonymised inserted into a SPSS data bank and will then be interpreted. For the adequate description of the collective data of gender, age, blood levels and medication will be gathered and added to the data bank anonymised. The calculated data will then be compared with the clinical evaluation of the patients with symptomatic irritable bowel syndrome, active inflammatory bowel diseases and patients with other gastrointestinal diseases. The aim of this study is to develop improved methods for non invasive diagnostics of gastrointestinal diseases.

Interventions

DIAGNOSTIC_TESTTesting Fecal Biomarkers In Comparison To Endoscopic Examination With Confocal Laser Endomicroscopy

Patients, who were examined during a routine diagnostics, should submit an extra morning stool sample up to two weeks before or after the gastroscopy and/or coloscopy to generate the data of the fecal biomarker mentioned above.

Sponsors

Sozialstiftung Bamberg
CollaboratorOTHER
Enterosan Labor LS SE & Co.KG
CollaboratorUNKNOWN
Universität Duisburg-Essen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults * Signed declaration of consent * Presence of a confirmed diagnosis of 1. Inflammatory bowel diseases 2. Irritable bowel syndrome 3. Gastrointestinal diseases, except participants with diagnosis of group 1 or 2 (e.g. celiac disease, food allergies, microscopic colitis, diverticulosis, diverticulitis) 4. Healthy controls as part of a preventive medical check-up

Exclusion criteria

* No indication for endoscopic examination as part of routine care * Age under 18 years

Design outcomes

Primary

MeasureTime frameDescription
correlation analysesdata of biomarkers generated two weeks before or two weeks after the gastroscopy and/or coloscopyCorrelation analyses will be performed to determine if there is a correlation between fecal biomarker values and confocal laser endomicroscopy results and histologic scores. If available, correlations between the fecal biomarkers and other parameters such as clinical activity index (CAI), Mayo score/disease activity index (DAI), endoscopic Rachmilewitz index (REI), and inflammatory bowel disease questionnaire (IBDQ) data will also be calculated. In addition, group comparisons will be performed to test whether fecal biomarkers differ between (1) the different levels of the Nancy index and (2) the classification into patients in remission and patients with disease activity given according to histological assessment. Receiver operating characteristic (ROC) curves will also be used to determine optimal cut-offs and calculate sensitivity and specificity of fecal biomarkers.

Countries

Germany

Contacts

Primary ContactJost Langhorst, Prof.
jost.langhorst@sozialstiftung-bamberg.de0049951-50311251
Backup ContactÖzlem Öznur
oezlem.oeznur@sozialstiftung-bamberg.de0049951-50316936

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026