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Набор скоро начнётся NCT07640659

Using Breath Tests to Study Gut Sulfur Changes During Dietary Therapy

Без фазы С лечением Ulcerative Colitis (UC)

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Elemental formula (mBiota Elemental, Good LFE, Santa Monica, CA), Reduced Sulfur diet, Habitual Diet.
Кому может быть актуально
Состояния в реестре: Ulcerative Colitis (UC). Базовые параметры: 19 лет — 70 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Канада
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Sulfur on the Breath: Using Breath Biomarkers to Monitor Gut Microbial Sulfur Metabolism During Elemental and Reduced Sulfur Dietary Therapy

Обзор

This study aims to test whether a short liquid-based diet, followed by a low-sulfur eating plan, is safe, manageable, and helpful for people with mild to moderate ulcerative colitis. Investigators want to see if this approach can improve gut health, lower inflammation, and reduce symptoms. Investigators will also test breath samples as an easy, non-invasive way to track gut bacteria activity and disease changes. Investigators believe this diet plan can reduce harmful gut bacteria that produce irritating sulfur compounds, leading to better gut health and measurable improvements that can be detected through breath testing.

Подробное описание

Purpose To determine whether a short-term elemental diet followed by a reduced sulfur diet is a safe, tolerable, and effective non-pharmacologic strategy to improve clinical outcomes, reduce inflammation, and beneficially modulate the gut microbiome in adults with mild-to-moderate ulcerative colitis. A secondary purpose is to validate breath-based biomarkers as non-invasive tools to monitor sulfur metabolism and disease activity. Breath biomarkers include volatile organic compounds (VOCs) and exhaled breath condensate (EBC) to assess sulfur-related metabolites.

Hypothesis A 2-week elemental diet followed by a 10-week reduced sulfur diet will reduce intestinal inflammation and improve clinical outcomes by shifting the gut microbiome away from pro-inflammatory, sulfur-metabolizing bacteria, resulting in reduced sulfur metabolite production detectable through exhaled volatile organic compounds and exhaled breath condensate.

Justification Despite advances in biologic therapies, many UC patients fail to achieve sustained remission, and current treatments do not address upstream drivers such as diet-microbiome interactions. Elemental diets have demonstrated efficacy in Crohn's disease but remain understudied in UC. Emerging evidence links dietary sulfur, microbial sulfur metabolism, and toxic metabolites to UC pathogenesis. This study addresses critical gaps by testing a feasible dietary intervention and validating non-invasive breath biomarkers for real-time disease monitoring and precision nutrition.

Objectives

* Evaluate the clinical efficacy, safety, and feasibility of an elemental diet followed by an reduced sulfur diet. * Characterize changes in gut microbiome composition, inflammatory markers, and sulfur-related metabolic outputs. * Validate breath-based volatile organic compounds and exhaled breath condensate as biomarkers of sulfur metabolism and treatment response. * Identify microbial and metabolic signatures predictive of dietary response.

Research Design A prospective, randomized, controlled trial in adults with mild-to-moderate UC. All participants complete a 2-week elemental diet, followed by randomization (2:1) to either a reduced sulfur diet group (intervention group) or return to habitual diet group (control group) for 10 weeks. Clinical indices, inflammatory biomarkers, stool microbiome profiles and breath samples are collected longitudinally. The initial 2-week elemental diet is applied uniformly to standardize baseline microbial and metabolic conditions prior to randomization and does not replace or delay clinical care decisions.

Statistical Analysis Primary outcomes will be assessed using within- and between-group comparisons of clinical and biochemical response at week 12. Microbiome and metabolomic data will be analyzed using multivariate and differential abundance methods. Correlations between breath biomarkers, microbiome features, and clinical outcomes will assess sensitivity and specificity.

Вмешательства

  • Пищевая добавка Elemental formula (mBiota Elemental, Good LFE, Santa Monica, CA)
    Elemental liquid diets (EDs) are a subset of Exclusive Enteral Nutrition (EEN). Similar to EEN, they are nutritionally complete formulas, but differ in that they consist of free amino acids, monosaccharides, and fatty acids instead of whole, intact macronutrients, which are designed for optimal digestibility and to minimize antigenicity. EDs have been shown to reduce immune activation, favourably modulate the microbiota, suppress proinflammatory cytokines, support epithelial repair, and exclude
  • Поведенческое Reduced Sulfur diet
    This diet excludes high sulfur foods (e.g., red meat, seafood, eggs), cruciferous vegetables, dried fruits, and fermented beverages. It also accounts for sulfate intake from drinking water and processed food additives.
  • Поведенческое Habitual Diet
    Participants randomized to the comparator group will continue their usual dietary intake for 10 weeks without specific dietary restrictions.

Первичные конечные точки

  • Composite clinical and biochemical response [Срок оценки: Baseline, Week 2 and week 12]
Вторичные конечные точки (11)
  • Stool Biomarkers [Срок оценки: Baseline, week 2 and week 12]
  • C-Reactive Protein (CRP) concentration [Срок оценки: Baseline, week 2 and week 12]
  • Complete Blood Count (CBC) parameters [Срок оценки: Baseline, week 2 and week 12]
  • Serum inflammatory biomarker concentrations [Срок оценки: Baseline, week 2 and week 12]
  • Breath Biomarkers [Срок оценки: Baseline, week 2 and week 12]
  • Adherence to the Elemental Diet and Reduced Sulfur Diet Intervention [Срок оценки: Baseline, week 2 and week 12]
  • Change in Quality of Life [Срок оценки: Baseline, week 2 and week 12]
  • Change in Anxiety [Срок оценки: Baseline, week 2 and week 12]
  • Change in Depression [Срок оценки: Baseline, week 2 and week 12]
  • Change in Weight [Срок оценки: Baseline, week 2 and week 12]
  • Change in Body Mass Index (BMI) [Срок оценки: Baseline, week 2 and week 12]

Критерии участия

Критерии включения

  • Age 19-70 years.

=Diagnosis of mild-to-moderate ulcerative colitis, defined by a partial Mayo score (pMayo) of 2-7.

  • Evidence of active inflammation at enrollment, defined as:
  • C-reactive protein (CRP) > 5 mg/L; or
  • Fecal calprotectin (FCP) > 200 µg/g.
  • Receiving stable medical therapy for ulcerative colitis for at least 8 weeks prior to enrollment.
  • No corticosteroid use at the time of recruitment.
  • Under consideration by the treating physician for treatment escalation or biologic switch due to inadequate response to current therapy.

Критерии исключения

  • Partial Mayo score (pMayo) > 7.
  • Pregnant or breastfeeding.
  • Body mass index (BMI) < 18 kg/m².
  • History of an eating disorder.
  • Severe psychiatric disorder.
  • Severe medical conditions, including:
  • Active cancer;
  • Significant cardiovascular disease;
  • Diabetes mellitus; or
  • Severe food allergies.
  • Known allergy or intolerance to corn, dextrose, or maltodextrin.
  • Antibiotic use within 3 months prior to enrollment.
  • Probiotic use within 3 months prior to enrollment.
  • Use of herbal anti-inflammatory supplements during the study period, including but not limited to:
  • Serrapeptidase;
  • Curcumin;
  • Boswellia; or
  • Bromelain.
  • History of major gastrointestinal surgery, including:
  • Ostomy;
  • Total colectomy; or
  • Short bowel syndrome.
  • Inability or unwillingness to comply with study procedures, including anticipated travel or other commitments that may interfere with participation.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Лечение

Центры проведения

Канада · 1 центр
  • University of British Columbia-Okanagan — Kelowna

Идентификаторы

NCT: NCT07640659 · H26-00017 · POP25-11968

Первоисточники (государственные реестры)

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