VENUS: Research on Vaginal Microbiota Evaluation Unified Standards Based on Gram Staining

Sponsor
Tianjin Medical University General Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05997160
Collaborator
Jiangsu Bioperfectus Technologies Co., Ltd (Other)
5,590
21.9

Study Details

Study Description

Brief Summary

The goal of this observational study is to explore a standardized sample process for improving the accuracy of vaginal microbiota evaluation and to explore a more complete and comprehensive method for vaginal microbiota evaluation based on gram staining.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study consists of two sub-studies:
    1. Sub-study on Standardized method of Microscopic Slide Preparation: this sub-study aims to compare different slide preparation methods and dilution levels based on various aspects, including uniformity, impurities, clarity and so on, and then explore the optimal method and dilution level. Additionally, it will summarize the conversion method for white blood cells between wet mount and gram staining, and for white blood cells between high-power microscopy and oil immersion microscopy.

    2. Sub-study on Vaginal Microbiota Evaluation on Gram Staining: For patients with diagnosed vaginal infection type, it will calculate the consistency of results between different laboratories. And it will evaluate the effectiveness combined artificial intelligence technology and other technological platforms. Besides, for patients without diagnosed vaginal infection type, different methods such as 16S rRNA gene sequencing and metagenomic sequencing are used for analysis and profiling to guide treatment.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    5590 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Research on Vaginal Microbiota Evaluation Unified Standards Based on Gram Staining
    Anticipated Study Start Date :
    Sep 1, 2023
    Anticipated Primary Completion Date :
    Jun 30, 2025
    Anticipated Study Completion Date :
    Jun 30, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    hospital name + infection type + number

    There is no intervention.

    Outcome Measures

    Primary Outcome Measures

    1. The score for smear [December 2023]

      This score consists of uniformity, impurities, cell degeneration, and clarity for evaluating a smear.

    2. Diagnosis of vaginitis type [March 2024]

      The Diagnosis of vaginitis type based on Gram-stained smear and antigen testing, including aerobic vaginitis(AV), bacterial vaginosis (BV), vulvovaginal candidiasis (VVC), trichomonal vaginitis (TV), and normal.

    3. Relative Abundance [May 2024]

      Relative Abundance is from 16S rRNA gene sequencing and metagenomic sequencing for patients without clearly diagnosis.

    4. Intensity [May 2024]

      The intensity is tested by liquid chromatography-tandem mass spectrometry for targeted metabolites for patients without clearly diagnosis.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years to 49 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Non-pregnant women who visit our research settings and conduct vaginal discharge examination based on Gram-stained smear.

    • No sexual intercourse, vaginal douching, or vaginal medication within the last 72 hours.

    • Not during menstruation (menstrual period ended ≥3 days ago).

    exclusion Criteria:

    • Receiving systemic or vaginal antifungal or antibiotic treatment within the past week.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Tianjin Medical University General Hospital
    • Jiangsu Bioperfectus Technologies Co., Ltd

    Investigators

    • Principal Investigator: Fengxia Xue, PhD, Tianjin Medical University General Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fengxia Xue, Director of the Medical Center for Obstetrics and Gynecology, Tianjin Medical University General Hospital
    ClinicalTrials.gov Identifier:
    NCT05997160
    Other Study ID Numbers:
    • IRB2023-YX-022-01
    First Posted:
    Aug 18, 2023
    Last Update Posted:
    Aug 18, 2023
    Last Verified:
    Aug 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Aug 18, 2023