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临床试验/NCT04698109
NCT04698109已完成不适用

Costituzione Della Biobanca Del Microbiota Intestinale e Salivare Umano: Dalla Disbiosi Alla Simbiosi

Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari1 个研究点 分布在 1 个国家目标入组 103 人开始时间: 2021年2月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
103
试验地点
1
主要终点
Biological samples collection for establishment of the first National Microbiome Biobank

研究概览

简要总结

This is a prospective, clinical, monocentric study aimed to collect biological samples and study microbiota from subjects suffering from subjects with recurrent cervicovaginitis, subjects with endometriosis, subjects with repeated implantation failures and from healthy volunteers. Microbiota is a complex consortium of microorganisms, located at the mucosal level (in particular intestinal, oral and vaginal) having a key role in human health and in the onset of several diseases. Microbiota alterations have been found in several diseases (gastrointestinal, metabolic, renal, oncological, gynaecological).

The study will allow to:

  • Provide biological samples (faeces, saliva, vaginal, urine) from healthy volunteers and patients suffering from selected disease to the first Italian microbiota biobank;
  • Study microorganisms using different in vitro and in vivo techniques;
  • Study the link between the microbiota and the disease. This study is part of the BIOMIS project (Project Code: ARS01_01220), presented as part of the "Avviso per la presentazione di progetti di ricerca industriale e sviluppo sperimentale nelle 12 aree di specializzazione individuate dal PNR 2015-2020" and admitted to funding under the National Operational Program "Ricerca e Innovazione" 2014-2020 by directorial decree of MIUR - Department for Higher Education and Research - n. 2298 of 12 September 2018. BIOMIS includes several clinical studies that enrol patients with different pathologies to collect and store biological samples and study microbiota.

详细描述

The primary aim of this monocentric study is to populate the first national microbioma biobank with biological samples (fecal, salivary, urinary and vaginsl samples) subjects suffering from selected disease disease and healthy volunteers.

The secondary aim is the characterization of microorganisms of the biobank and study of the microbiota-pathology relationship using meta-omics, in vitro and in vivo approaches, The study plans to enrol 100 subjects at Policlinic of Bari, according to the inclusion/exclusion criteria. The study participation is voluntary, and the subjects have the right to withdraw from the study at any time and for any reason.

During the study, 3 visits are planned:

  • Visit 0 (V0), including description of the objectives and procedures study, signature written informed consent, inclusion/exclusion criteria evaluation, medical examination (blood pressure measurement, abdominal and thoracic physical examination), filling in of the anamnestic questionnaire, delivery of kits for the collection of fecal, salivary and urinary material to be reported at Visit 1 and delivery of a 3-day food diary, to be completed autonomously in the days preceding the Visit 1.
  • Visit 1 (V1) - at least 4 days after V0, including delivery of the of the collected biological material (feces, saliva, urine), and of a 3-day food diary, filling in of the new signs and symptoms anamnestic questionnaire and collection of the vaginal swab by medical staff.
  • Telephone evaluation: administration of a "Food Frequency Questionnaire" to assess the subjects' alimentary habits.

Standard Operative Procedures (SOP) for samples storing, transport and processing will be adopted to ensure samples stability and grant results validity and quality.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • HEALTHY VOLUNTEERS
  • healthy subjects aged between 18 and 45 years, in reproductive age
  • BMI between 18.5-30
  • omnivorous diet
  • signature of the informed consent
  • PATIENTS WITH RECIDIVING CERVIC VAGINITIS
  • healthy subjects aged between 18 and 45 years, in reproductive age
  • Patients suffering from at least 3 episodes of relapsing cervicovaginitis per year: diagnosis of anaerobic vaginitis (AV) or bacterial vaginosis (BV) or vulvo-vaginal candidiasis (VVC) based on clinical symptoms and positive microscopic examination and / or positive vaginal culture
  • BMI between 18.5-30
  • omnivorous diet
  • signature of the informed consent
  • PATIENTS WITH ENDOMETRIOSIS
  • Inclusion criteria:
  • aged between 18 and 45 years, in reproductive age
  • patients with endometriosis: diagnosis of endometriosis carried out with transvaginal ultrasound with associated elevation of CA125
  • BMI between 18.5-30
  • omnivorous diet
  • signature of the informed consent
  • PATIENTS WITH REPEATED IMPLANT FAILURES (RIF)
  • Inclusion criteria:
  • age between 18 and 45 years in reproductive age
  • patients with RIF: patients who have followed PMA protocols with at least 3 failed attempts after transfer of good quality embryos
  • BMI between 18.5-30
  • omnivorous diet
  • signature of the informed consent

排除标准

  • HEALTHY VOLUNTEERS
  • Current or previous infectious diseases (HAV, HBV, HCV, HIV, Cytomegalovirus, Epstein-Barr virus)
  • HPV positive
  • Chronic liver disease
  • History of Clostridium difficile infections
  • Recent (<3 months) therapy with antibiotics, immunosuppressive drugs, chemotherapy
  • Chronic therapy with proton pump inhibitors
  • Recent (<3 months) use of probiotics, laxatives or other aids (drugs / supplements) for the regulation of gastrointestinal activity
  • Previous history of organ / tissue transplantation
  • Recent onset of diarrhea
  • Chronic diarrhea
  • Chronic constipation
  • Previous gastrointestinal surgery (eg gastric bypass)
  • Recurring urinary tract infections (3 cases per year)
  • Previous major acute cardiovascular diseases (myocardial infarction, stroke)
  • Type 2 diabetes mellitus
  • Hypertension
  • eGFR (estimated glomerular filtration rate) lower than 60ml / minute and / or diagnosis of nephropathy
  • Chronic gastrointestinal disorders
  • Systemic inflammatory diseases
  • Suspicion, clinical diagnosis or previous history of cancer (<5 years)
  • Autoimmune disorders or history of chronic and systemic autoimmune disorders
  • Neurodegenerative disorders
  • Pregnancy and breastfeeding
  • Hormonal and / or intrauterine contraceptive therapy
  • Healthcare workers
  • Operators work with animals
  • Psychiatric conditions that reduce protocol compliance.
  • Exclusion criteria:
  • POPULATION 2 - PATIENTS WITH RECIDIVING CERVIC VAGINITIS/ POPULATION 3 - PATIENTS WITH ENDOMETRIOSIS/ POPULATION 4 - PATIENTS WITH REPEATED IMPLANT FAILURES (RIF)
  • Current or previous infectious diseases (HAV, HBV, HCV, HIV, Cytomegalovirus, Epstein-Barr virus)
  • Chronic liver disease
  • History of Clostridium difficile infections
  • Recent (<3 months) therapy with antibiotics, immunosuppressive drugs, chemotherapy
  • Chronic therapy with proton pump inhibitors
  • Recent (<3 months) use of probiotics, laxatives or other aids (drugs / supplements) for the regulation of gastrointestinal activity
  • Previous history of organ / tissue transplantation
  • Recent onset of diarrhea
  • Chronic diarrhea
  • Chronic constipation
  • Previous gastrointestinal surgery (eg gastric bypass)
  • Recurring urinary tract infections (3 cases per year)
  • Previous major acute cardiovascular diseases (myocardial infarction, stroke)
  • Type 2 diabetes mellitus
  • Hypertension
  • eGFR (estimated glomerular filtration rate) lower than 60ml / minute and / or diagnosis of nephropathy
  • Chronic gastrointestinal disorders
  • Systemic inflammatory diseases
  • Suspicion, clinical diagnosis or previous history of cancer (<5 years)
  • Autoimmune disorders or history of chronic and systemic autoimmune disorders
  • 另有 6 项未显示

结局指标

主要结局

Biological samples collection for establishment of the first National Microbiome Biobank

时间窗: through study completion, an average of 1 year

Recruitment of 100 subjects (patients with recurrent cervicovaginitis, endometriosis, repeated implantation failures and healthy volunteers) to collect biological samples for establishment of the first National Microbiome Biobank

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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