- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT06548009
Método baseado no metabolismo sérico para diagnosticar diarreia por ácidos biliares
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.
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Inscrição (Real)
Contactos e Locais
Locais de estudo
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Copenhagen, Dinamarca
- Bispebjerg and Frederiksberg Hospital
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Hellerup, Dinamarca
- Herlev Gentofte Hospital
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Hillerød, Dinamarca
- Hillerød Hospital
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
The study population consists of SeHCAT referred patients for suspected bile acid diarrhoea.
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Modelos de observação: COHORT
- Perspectivas de Tempo: PROSPECTIVE
Coortes e Intervenções
Grupo / Coorte |
Intervenção / Tratamento |
|---|---|
|
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 |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
AUROC curve of the BDS in the validation cohort
Prazo: 1 year from now
|
AUROC curve of the BDS in the validation cohort |
1 year from now
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Curva AUROC de BDS em pacientes com cada um dos três subtipos de TAB
Prazo: Daqui a 1 ano
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Daqui a 1 ano
|
|
Curva AUROC de BDS na coorte de descoberta (ver 8.2 Análise de dados)
Prazo: Daqui a 1 ano
|
Daqui a 1 ano
|
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Correlação do resultado do teste SeHCAT com a gravidade dos sintomas de TAB
Prazo: Daqui a 1 ano
|
Daqui a 1 ano
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Correlação dos resultados do teste BDS com o número de evacuações por dia
Prazo: Daqui a 1 ano
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Daqui a 1 ano
|
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Biomarcadores para BAD: C4 e FGF19
Prazo: Daqui a 1 ano
|
Daqui a 1 ano
|
Colaboradores e Investigadores
Patrocinador
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- BAD-DIVA
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
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