Periodontal Microbiota of Patients Candidates for Bariatric Surgery With Body Mass Index Greater Than 30
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Bariatric Surgery, Obesity, Morbid. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
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
Overview
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.
Detailed description
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.
Primary outcome measures
- Taxonomic analysis [Time frame: before bariatric surgery]
Eligibility criteria
Inclusion criteria
- 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,
Exclusion criteria
- 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
France · 1 center
- University Hospital of Toulouse — Toulouse
Identifiers
NCT: NCT06781229 · RC31/24/0432