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Diversity Analysis of Vaginal Microbiota on Women With High-risk Human Papillomavirus Infection

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ClinicalTrials.gov Identifier: NCT03548740
Recruitment Status : Unknown
Verified February 2019 by shuwang, Peking Union Medical College Hospital.
Recruitment status was:  Recruiting
First Posted : June 7, 2018
Last Update Posted : February 6, 2019
Sponsor:
Information provided by (Responsible Party):
shuwang, Peking Union Medical College Hospital

Study Description
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Brief Summary:
Since other genital infections enhance HIV susceptibility by inducing inflammation, the investigators study the relationship between the vaginal microbiota composition and the risk of HPV infection, cervical cytological abnormalities.

Condition or disease Intervention/treatment
Papillomavirus Infections Biological: Human Papillomavirus

Detailed Description:
Persistent infection with oncogenic Human Papillomavirus (HPV) is necessary but not sufficient for the development of cervical cancer. Additional factors correlated with HPV persistence include immunodeficiency caused by HIV, smoking, use of oral contraceptives and, more recently reported, vaginal dysbiosis. In a state of dysbiosis, there is a marked reduction of Lactobacillus and a high diversity of bacteria, with increased abundance of anaerobic bacterial species. Based on this, the investigators are going to analyze the changes of microbiota in women with high-risk HPV and the cervical lesions. And the investigators hope to figure out the difference and change in microbiota to realize the tanning of cervical lesions.
Study Design
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Study Type : Observational [Patient Registry]
Estimated Enrollment : 151 participants
Observational Model: Case-Control
Time Perspective: Prospective
Target Follow-Up Duration: 3 Years
Official Title: Diversity Analysis of Vaginal Microbiota on Women With High-risk Human Papillomavirus Infection and Cervical Cytological Abnormalities.
Actual Study Start Date : September 1, 2018
Estimated Primary Completion Date : January 20, 2020
Estimated Study Completion Date : May 20, 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HPV

Groups and Cohorts
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Group/Cohort Intervention/treatment
Group A Biological: Human Papillomavirus
women with high-risk Human Papillomavirus or not
Group B


Outcome Measures
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Primary Outcome Measures :
  1. Vaginal microbiota and HR-HPV infection [ Time Frame: 12 months ]
    The persistence vaginal organism in HPV infection participants

  2. Vaginal microbiota and the cervical lesion [ Time Frame: 12 to 36 months ]
    The cervical cytology, HPV and the vaginal microbiota were evaluated


Eligibility Criteria
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Ages Eligible for Study:   25 Years to 50 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Group A: HPV positive, and the participants who have not taken drugs and physical therapy in the past six months, nor have chronic diseases (such as DM), take their vaginal microorganisms (do not mention the past History issues). Group B: HPV negative in the past 12 months, taking the vaginal microorganisms.
Criteria

Inclusion Criteria:

Clinical diagnosis of HR-HPV results.

Exclusion Criteria:

Clinical diagnosis of vaginitis, immune disease, malignancy History of cervical lesions Pregnancy Clinical diagnosis of other serious systemic primary diseases, such as severe liver and kidney dysfunction Severe mental illness

Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03548740


Locations
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China, Beijing
Peking Union Medical College Hospital Recruiting
Beijing, Beijing, China, 100730
Contact: Shu Wang, associated professor    +86-136-7124-6680    wangshu219@hotmail.com   
Sponsors and Collaborators
Peking Union Medical College Hospital
More Information
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Additional Information:

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Responsible Party: shuwang, Associate Professor, Peking Union Medical College Hospital
ClinicalTrials.gov Identifier: NCT03548740    
Other Study ID Numbers: WS-1
First Posted: June 7, 2018    Key Record Dates
Last Update Posted: February 6, 2019
Last Verified: February 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Infections
Communicable Diseases
Papillomavirus Infections
Disease Attributes
 Pathologic Processes
DNA Virus Infections
Virus Diseases
Tumor Virus Infections