- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT06548009
Méthode basée sur les métabolismes sériques pour le diagnostic de la diarrhée acide biliaire
Bile acid diarrhoea (BAD) is a common yet under-diagnosed and under-recognised disease. The primary symptoms are watery diarrhoea with high frequency of unpredictable bowel movements,urgency and faecal incontinence making BAD a debilitating condition. One of the challenges of BAD is the lack of a readily available and accurate diagnostic test.
The aim of this study is to validate a BAD diagnostic score (BDS) based on metabolomics.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Bile acid diarrhoea (BAD) is a common yet under-diagnosed and under-recognised disease. The primary symptoms are watery diarrhoea with high frequency of unpredictable bowel movements,urgency and faecal incontinence making BAD a debilitating condition. The pathophysiology of BAD involves spill-over of bile acids to the colon where bile acids irritate the colonic mucosa and cause osmotic-induced fluid secretion. The aetiology of BAD can be either idiopathic (termed primary BAD or type 2 BAD) or the disease can develop secondary to ileal dysfunction (due to, e.g., intestinal surgery or Chron's disease, termed type 1 BAD) or other conditions interfering with ileal absorption (due to, e.g., cholecystectomy or radiation therapy, termed type 3 BAD).
Irritable bowel syndrome (IBS) with predominant diarrhoea is a common condition in the general population (prevalence of around 4%) and emerging data suggest that around 1/3 suffering from this condition in fact have BAD. Many of these patients remains undiagnosed and thus,inappropriately treated or even untreated. A major reason for this is challenges associated with diagnosing BAD. Several diagnostic modalities have been suggested including 14C-glycocholate breath test, stool test and assessment of 48-hour faecal bile acid output. These tests are cumbersome, time-consuming, and not widely available. The 75selenium homocholic acid taurine (SeHCAT) test is considered the gold standard for the diagnosis of BAD. It measures, via a standard gamma camera, the 7-day retention of a taurine-conjugated bile acid analogue labelled with the gamma-emitter 75selenium. This test provides a quantitative assessment to estimate the severity of BAD, but there is no general agreement regarding its cut-off value and the test is not widely available or even approved for clinical use in many countries outside Europe, including the USA. Furthermore, the SeHCAT test is cumbersome due to its dependence on two visits to the clinic exactly seven days apart, it is expensive, and involves radioactive exposure to the patient. Given the limited availability and the challenges associated with the abovementioned tests, excluding BAD is unfortunately not within current routine investigational algorithms for diarrhoea-predominant IBS, Crohn's disease, or gastrointestinal cancers. In many cases, BAD diagnosis is considered after therapeutic trial using bile acid sequestrants. However, these agents are expensive, often ineffective and/or associated with gastrointestinal side effects in patients with established BAD why their potential as diagnostic tools is limited. Taken together, diagnosing BAD is currently associated with challenges that may preclude relevant treatment of this debilitating condition warranting development of easy and accessible yet safe and effective BAD diagnostics. Recently, the investigators have developed a new BAD diagnostic method based on a single blood sample from the patient. Our approach is based on unbiased, metabolic profiling of serum from BAD patients and carefully matched healthy individuals using comprehensive ultra-high-performance liquid chromatography time-of-flight mass-spectrometry. These comprehensive datasets were subjected to state-of-the-art machine learning and used to build a BAD diagnostic score (BDS) that can distinguish a patient suffering BAD from healthy individuals with high precision (sensitivity of 78% and specificity of 93%). In the present study, the investigators will refine the BDS to distinguish between patients suffering from BAD and patients suffering from other diarrhoeal diseases by using the same methods and data analyses as in the previous project, but in this case applied to serum samples collected from patients referred to diagnostic SeHCAT test, i.e., samples from both test-positive and test-negative patients.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
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-
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Copenhagen, Danemark
- Bispebjerg and Frederiksberg Hospital
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Hellerup, Danemark
- Herlev Gentofte Hospital
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Hillerød, Danemark
- Hillerød Hospital
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
The study population consists of SeHCAT referred patients for suspected bile acid diarrhoea.
La description
Inclusion Criteria:
- SeHCAT referral for suspected bile acid diarrhoea
- Age ≥18 years
Exclusion Criteria:
- Diabetes, except type 2 diabetes
- Nephropathy with estimated glomerular filtration rate <30 min/1.73 m2
- Treatment with medicine that cannot be paused for 12 hours
- Hypothyroidism or hyperthyroidism, if not well regulated
- Active or recent (<6 months since last treatment) malignant disease
- Any treatment or condition requiring acute or subacute medical or surgical intervention
- Any condition considered incompatible with trial participation by the investigators
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Modèles d'observation: COHORT
- Perspectives temporelles: PROSPECTIVE
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
SeHCAT confirmed bile acid diarrhea
Patients referred to a SeHCAT scan due to suspected bile acid diarrhea, who afterwards turned out to be suffering from SeHCAT confirmed bile acid diarrhea |
Blood samples taken with the objective of identifying a diagnostic test |
|
SeHCAT negative patients
Patients referred to a SeHCAT scan due to suspected bile acid diarrhea, who afterwards turned out to be SeHCAT negative |
Blood samples taken with the objective of identifying a diagnostic test |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
AUROC curve of the BDS in the validation cohort
Délai: 1 year from now
|
AUROC curve of the BDS in the validation cohort |
1 year from now
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Courbe AUROC du BDS chez les patients présentant chacun des trois sous-types de BAD
Délai: Dans 1 an
|
Dans 1 an
|
|
Courbe AUROC du BDS dans la cohorte découverte (voir 8.2 Analyse des données)
Délai: Dans 1 an
|
Dans 1 an
|
|
Corrélation du résultat du test SeHCAT avec la gravité des symptômes de MAUVAIS
Délai: Dans 1 an
|
Dans 1 an
|
|
Corrélation des résultats du test BDS avec le nombre de selles par jour
Délai: Dans 1 an
|
Dans 1 an
|
|
Biomarqueurs du BAD : C4 et FGF19
Délai: Dans 1 an
|
Dans 1 an
|
Collaborateurs et enquêteurs
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- BAD-DIVA
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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