Human Internal BIOASTER's Samples Collection

Not yet recruiting

• Conditions: Biological Samples
• Interventions: Other: Biological sampling

• Registration Number: NCT06602388
• Lead Sponsor: Bioaster

Brief Summary

BIOASTER is a Technological Research Institute dedicated to microbiology and infectious diseases. BIAOSTER\'s areas of expertise are organized around four research programs: 1/ Antimicrobials; 2/ Vaccines; 3/ Microbiota; 4/ Diagnostics.

Hibiscus is a non-interventional, monocentric study aimed at building up a a collection of biological samples (stool, urine, saliva, buccal swab, nasal swab, superficial skin swab, hair) collected from BIOASTER employees. These samples to be used for scientific purposes including the technological development of Bioaster\'s collaborative and in-house research projects.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-09
• Study First Submitted: 2024-09-16
• Study First Submitted QC: 2024-09-16
• Last Update Submitted: 2024-09-16
• Study First Posted: 2024-09-19
• Last Update Posted: 2024-09-19
• Study Start: 2024-12-30
• Primary Completion: 2027-12-31
• Study Completion: 2027-12-31

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Some inclusion criteria can be defined according to the needs of the scientific objective. For example, it is up to volunteers to decide whether or not to participate if they meet the following criteria:

• Age criteria (e.g.: specific, non-identifying range sought: 30-40 years)
• BMI criteria (for example: BMI between 18.5 and 29 kg/m2)
• Gender criteria (e.g.: women only)

Exclusion Criteria

Some of the following non-inclusion criteria may be defined according to the needs of the project:

• Minor subject
• Health criteria (e.g. presence or absence illness/infection/vaccination/allergy/anti-infective treatment in the last 3 months prior to the date of sampling)
• Smoker status
• Severe chronic illness (active cancer, HIV, severe renal failure, ongoing severe heart, liver or biliary disorders, arthritis)
• Diagnosed acute or chronic gastrointestinal disease or complication (e.g. celiac disease, gastroesophageal reflux, gastric or duodenal ulcer, Crohn's disease, hemorrhoids, irritable bowel syndrome),

In all cases, it will be requested that volunteers with the following criteria do not participate in the study:

• Pregnant or breast-feeding women
• Subjects under curatorship or guardianship
• Subjects under legal protection.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Healthy volunteers (Bioaster employees)	Biological sampling	Collection of biological samples from healthy volunteers: Stool, urine, saliva, buccal swab, nasal swab, superficial skin swab, hair

Primary Outcome Measures

Name	Time	Method
The number of analyzable samples collected for scientific purposes.	3 years after the first inclusion	The number of analyzable samples collected for scientific purposes at the end of inclusion periode