Меню
Набор скоро начнётся NCT06642766

Fiber Product for Gas, Bloating, and Bowel Regularity

Без фазы С лечением Bloating Bowel Irregularities Bowel Gas

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: Fiber supplement.
Кому может быть актуально
Состояния в реестре: Bloating, Bowel Irregularities, Bowel Gas. Базовые параметры: 18 лет — 90 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
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Open Label Study of a Novel, Commercially Available Fiber Product for Gas, Bloating, and Bowel Regularity

Обзор

This is a new, commercially available, over-the-counter fiber supplement that combines 8 fibers. The varied nature of the fibers in this product is designed to create a more diverse microbiome (bacteria that live within the human GI tract). In general, the more diverse the microbiome the less inflammatory the gut. The purpose of this study is to evaluate the effects of a new fiber product on bloating, gas, and bowel movements.

Вмешательства

  • Пищевая добавка Fiber supplement
    Subjects that meet the inclusion criteria and with symptoms appropriate for fiber supplementation are eligible to participate. Participants will be instructed to use the fiber product (NutraLieve) as currently labeled; start with a dosage of 4-5 grams per day (one heaping teaspoon), initially taken once daily, increasing up to 3 heaping teaspoons a day (maximum dose 15 grams/day) on an as needed basis.Participants will be prospectively assessed for symptoms at baseline and at 6 weeks. * The pri

Первичные конечные точки

  • Number of bowel movement [Срок оценки: 6 weeks]
Вторичные конечные точки (2)
  • Bloating [Срок оценки: 6 weeks]
  • Gas [Срок оценки: 6 weeks]

Критерии участия

Критерии включения

  • Subjects have experienced two or more of the following criteria for at least 3 months with symptom onset at least 6 months prior: straining during at least 25% of defecations, lumpy or hard stools in at least 25% of defecations, sensation of incomplete evacuation for at least 25% of defecations, sensation of anorectal obstruction/blockage for at least 25% of defecations, manual maneuvers to facilitate at least 25% of defecations (e.g., digital evacuation, support of the pelvic floor), loose stools are rarely present without the use of laxatives Or,
  • Subjects have experienced 2 or more of the following criteria of recurrent abdominal pain, for at least 3 months, with symptom onset at least 6 months prior: pain related to defecation, associated with a change in frequency of stool, associated with a change in form (appearance) of stool Or,
  • Subjects have experienced 2 or more of the following criteria for at least 3 months, with symptom onset at least 6 months prior: recurrent abdominal pain, on average, at least 1 day per week in the last 3 months associated with two of the following criteria: pain related to defecation, pain associated with a change in frequency of stool and pain associated with a change in form (appearance) of stool.
  • The subject predominantly experiences loose or watery stools (Bristol Stool Form Scale types 6-7), more than 25% of the time, or hard or lumpy stools (types 1-2) less than 25% of the time.
  • The symptoms should be chronic and interfere with daily activities, cause worry or affect the quality of life.

Критерии исключения

  • Loose stools are present for more than 25% of defecations
  • Unable to provide informed consent
  • Hematochezia
  • Prior colon surgery
  • Thyroid disease
  • Pelvic floor disorder
  • Known allergies or intolerance to fiber products
  • infectious diarrhea or food poisoning
  • inflammatory bowel disease, including microscopic colitis
  • fecal incontinence or rectal prolapse

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Поддерживающая терапия

Центры проведения

США · 1 центр
  • XL Medical — Edina

Идентификаторы

NCT: NCT06642766 · 20243173

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗