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Analysis of Ameliorative Effects of Oral Probiotics on Bacterial Vaginosis

NCT03116789 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 43

Last updated 2020-02-05

No results posted yet for this study

Summary

The purpose of this study is to analyze the ameliorative effects of oral probiotics on bacterial vaginosis.

Conditions

  • Bacterial Vaginosis

Interventions

DIETARY_SUPPLEMENT

probiotics

Two capsules for daily

Sponsors & Collaborators

  • Kuo General Hospital

    collaborator OTHER

  • GenMont Biotech Incorporation

    lead INDUSTRY

Principal Investigators

  • Ta-Chin Lin · Kuo General Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-11
Primary Completion
2019-12-31
Completion
2019-12-31

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03116789 on ClinicalTrials.gov