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Идёт набор NCT06781229

Periodontal Microbiota of Patients Candidates for Bariatric Surgery With Body Mass Index Greater Than 30

Наблюдательное Bariatric Surgery Obesity, Morbid

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
Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
Кому может быть актуально
Состояния в реестре: Bariatric Surgery, Obesity, Morbid. Базовые параметры: от 18 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
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Non-interventional Study Exploring the Composition of the Periodontal Microbiota of Patients With Body Mass Index Greater Than 30 That Are Candidates for Bariatric Surgery

Обзор

The goal of this observational study is to compare the microbiological composition of the periodontal plaque of obese people undergoing bariatric surgery according to their Body Mass Index. The main question it aims to answer is: Does obese patients have different microbiote according to their obesity? Obesity being classified in two groups : * group "obesity" for a BMI between 30 and 35 * versus "morbid obesity" group with a BMIabove 35. Participants who are scheduled to undergo bariatric surgery as part of their regular medical care will answer questions about their quality of life, hygiene habits, and saliva and periodontal samples will be taken.

Подробное описание

The study is a non-interventional, single-centre, cross-sectional, comparative study with prospective and consecutive recruitment of participants.

Participants who are scheduled to undergo bariatric surgery as part of their regular medical care will

1. during the odontological visit of approximately one hour:

* complete standard odontology medical questionnaire * complete the dietary hygiene questionnaire: "Etude Nationale Nutrition Santé" questionnaire * complete 2 quality of life questionnaires: EQ-5D-5L questionnaire and GOHAI self-questionnaire * undergo clinical examination (visual examination and partial periodontal probing), * Radiological check-up (panoramic X-ray) and biological check-up (salivary and periodontal samples (non-invasive). 2. During bariatric surgery, surgical techniques create surgical waste. From this operative waste, fragments of visceral adipose tissue may be recovered and, if the surgery so requires, subcutaneous adipose tissue (quantity recovered: 5g of visceral adipose tissue and 5g of subcutaneous adipose tissue). The samples taken will be stored in a hospital tissue bank with a view to possible future re-use. Each patient will be informed of this during the inclusion visit.

Первичные конечные точки

  • Taxonomic analysis [Срок оценки: before bariatric surgery]

Критерии участия

Критерии включения

  • BMI greater than or equal to 30
  • Be on the list of patients scheduled for bariatric surgery,
  • Be able to receive information about the study and understand the information form in order to take part in the study. This implies mastering the French language,

Критерии исключения

  • Alcohol consumption >30g/d (men) or 20g/d (women),
  • Having taken antibiotics, prebiotics or probiotics in the month prior to inclusion (this has an influence on the composition of the patient's microbiota),
  • During pregnancy or breastfeeding,
  • For whom oral surgery is planned (surgery for benign or malignant tumours of the maxillary and mandibular bone bases), or with a history of oral surgery in the month prior to inclusion,
  • At risk of infection (existence of one or more of the following known chronic infectious diseases: HIV, HBV, HCV and mononucleosis) and/or chronic renal insufficiency (creatinine clearance < 60ml/min),
  • Patients with a general pathology that contraindicates the performance of diagnostic procedures such as periodontal probing (patients at high risk of infective endocarditis according to the ANSM).
  • Totally edentulous patients

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Франция · 1 центр
  • University Hospital of Toulouse — Toulouse

Идентификаторы

NCT: NCT06781229 · RC31/24/0432

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗