Vaginal Microbiome-host Interaction in Mesh Exposure After TVM Surgery

Sponsor
Peking Union Medical College Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05000112
Collaborator
(none)
50
36

Study Details

Study Description

Brief Summary

Transvaginal pelvic mesh implantation(TVM) is a foreign body implantation operation with intraoperative colonization of vaginal bacteria. However, the vaginal microbiome-host interaction and its influence in the mechanism of mesh exposure after TVM remains unclear. This study will enroll post-TVM patients with and without mesh exposure and use their vaginal swabs to perform TRACE-seq and cytokine analysis. The microbiome-host interactions related with mesh exposure and the changes in protein expression will be analyzed.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    50 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Official Title:
    The Influence of Vaginal Microbiome-host Interaction in the Mechanism of Mesh Exposure After Trans-Vaginal Mesh Implantation
    Anticipated Study Start Date :
    Sep 1, 2021
    Anticipated Primary Completion Date :
    Sep 1, 2023
    Anticipated Study Completion Date :
    Sep 1, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    Patients with mesh exposure

    During the physical examination, a speculum was inserted into the vagina to observe the vaginal epithelium for mesh exposure. If the mesh is seen on surface of the vaginal mucosa, the patient is diagnosed with mesh exposure.

    Patients without mesh exposure

    During the physical examination, a speculum was inserted into the vagina to observe the vaginal epithelium for mesh exposure. If the mesh is not seen on surface of the vaginal mucosa, bimanual examination will be performed to confirm no foreign body can be feeled on surface of the vaginal mucosa. Then the patient belong to this group.

    Outcome Measures

    Primary Outcome Measures

    1. Vaginal microbiome-host interaction in patients after TVM [Over 6 months postoperative]

    2. Vaginal microbiome-host Interaction associated with mesh exposure after TVM [Over 6 months postoperative]

    Secondary Outcome Measures

    1. Difference of vaginal microbiome between groups [Over 6 months postoperative]

    2. Differentially expressed genes in host-mesh interaction between groups [Over 6 months postoperative]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years to 100 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with "III-IV degree uterine/apex/anterior vaginal wall prolapse and I-II degree of posterior vaginal wall prolapse" who agree to be treated by transvaginal pelvic mesh implantation.

    • All surgeries were performed by surgeons with extensive experience in transvaginal mesh implantation (>20 vaginal mesh implantation per year) using macroporous, monofilament, polypropylene mesh.

    Exclusion Criteria:
      1. Have had sex in the past 5 days or had vaginal irrigation;
      1. Use oral or vaginal antibiotics, antifungal, immunosuppressant, hormone drugs or probiotics for the last 30 days.
      1. Combined with immunosuppressive diseases, diseases with contraindication of vaginal estrogen such as breast cancer, endometrial cancer.
      1. If the patient has a uterus before surgery and does not undergo total transvaginal hysterectomy during surgery,
      1. Intraoperative bladder injury or intraoperative hemorrhage >500ml or postoperative hematoma.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Peking Union Medical College Hospital

    Investigators

    • Principal Investigator: Lan Zhu, Peking Union Medical College

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Peking Union Medical College Hospital
    ClinicalTrials.gov Identifier:
    NCT05000112
    Other Study ID Numbers:
    • ZS-2936
    First Posted:
    Aug 11, 2021
    Last Update Posted:
    Sep 27, 2021
    Last Verified:
    Jul 1, 2021
    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 Sep 27, 2021