Vaginal Microbiome and the Development of Vulvovaginal Graft Versus Host Disease

Sponsor
Hadassah Medical Organization (Other)
Overall Status
Recruiting
CT.gov ID
NCT05316740
Collaborator
Rambam Health Care Campus (Other), Tel-Aviv Sourasky Medical Center (Other)
40
1
33.5
1.2

Study Details

Study Description

Brief Summary

Allogeneic stem cell transplantation (also termed "bone marrow transplantation") involves transferring stem cells from a healthy person (the donor) to the patient, after high-intensity chemotherapy or radiation, given to destroy any remaining cancer cells in the body. When a transplant is successful, the donor stem cells replace the original cells in the bone marrow. It may provide the only long-term cure of the patient's disease. Of transplant-related complications, graft-versus-host disease (GVHD) is one of the most important complications. GVHD arises from donor immune cells, that identify the recipient's (the patien's) cells as foreign and attack them. Approximately half of women undergoing transplantation will experience GVHD involving the genitalia (i.e., the vulva and vagina), termed vulvovaginal GVHD (VV-GVHD). VV-GVHD may cause irreversible anatomical changes, including complete vaginal obliteration, and not surprisingly, it has a severe impact on patients' quality of life and sexual function. This complication is unpredictable and non-preventable by the usual immunosuppressive treatment given to patients. Frequent gynecological examinations and prolonged follow-up of transplanted women are needed, to allow early diagnosis and prevention of harmful results of VV-GVHD. This follow-up adds inconvenience and anxiety to the patients.

The suggested study aims to evaluate a possible association between vaginal microorganisms (the "microbiome") to the progress of VV-GVHD. Finding such association may allow prediction of VV-GVHD progress, a better understanding of the development of VV-GVHD and a potential to develop interventions for the treatment and prevention of VV-GVHD.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Vaginal Microbiome and the Risk of Vulvovaginal Graft Versus Host Disease Following Hematopoietic Stem Cell Transplantation
Actual Study Start Date :
Feb 15, 2022
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Outcome Measures

Primary Outcome Measures

  1. Microbiome composition [2 years]

    Characterization of the vaginal microbial community using shotgun analysis and16S rRNA sequencing

  2. CMV presence [2 years]

    Evaluation of CMV in vaginal samples using PCR assay

  3. Vulvovaginal graft vs host disease presence [2 years]

    Evaluation of presence of vulvovaginal GVHD by gynecologic examination, using the NIH classification system for chronic graft-versus-host disease

Secondary Outcome Measures

  1. HPV presence [2 years]

    Evaluation of HPV in vaginal samples

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Ageā‰„18

  • Candidate for allogeneic stem cell transplantation

  • Ability to sign an informed consent

Exclusion Criteria:
  • Patient does not approve sample collection

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hadassah Medical Center Jerusalem Israel 9765422

Sponsors and Collaborators

  • Hadassah Medical Organization
  • Rambam Health Care Campus
  • Tel-Aviv Sourasky Medical Center

Investigators

  • Principal Investigator: Ahinoam Lev Sagie, MD, Hadassah Medical Organization

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT05316740
Other Study ID Numbers:
  • 0512-21-HMO
First Posted:
Apr 7, 2022
Last Update Posted:
Apr 7, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 7, 2022