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NCT02898818 Clinical Trial

Vaginal and Oral Microbiome Crosstalk

Healthy Clinical Trial

Official title:
EMMI - Emättimen Mikrobiomi - Emättimen ja Suun Limakalvojen Vuorovaikutus

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02898818
Other study ID # T146/2016
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 19, 2017
Est. completion date September 2026

Study information
Verified date April 2024
Source Turku University Hospital
Contact Niina K Hieta, MD, PhD
Phone 2-3131620
Email niina.hieta@tyks.fi
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To study the vaginal and oral microbiome by swab samples. On selected cases, also papa smear will be studied.

Description:

To study the vaginal and oral microbiome by swab samples and on selected groups, by papa smear test, to find out the constitution of normal and vaginal microbiome and the cross-talk between oral and vaginal mucosa. To find out about the impact of human papilloma virus on the microbiome and vice versa.

Recruitment information / eligibility
Status Recruiting
Enrollment 520
Est. completion date September 2026
Est. primary completion date September 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients coming to Turku University Hospital Dermato-Venereology or Gynaecology Departments or to family planning clinics in The wellbeing services county of Southwest Finland for previously mentioned reasons Exclusion Criteria: - those not meeting the criteria

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• vaginal and oral swab sample, questionnaire
vaginal and oral swab sample and questionnaire
• papa smear
Papnicolaou Papa Smear test

Locations
Country Name City State
Finland Turku University Hospital Turku

Sponsors (2)
Lead Sponsor Collaborator
Turku University Hospital Oulu University Hospital

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary microbiome, papa smear Differences in microbiome and papa smear 5 years
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