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SAFETY AND EFFICACY IN MANAGING VAGINAL INFECTIONS

Not Applicable
Conditions
Health Condition 1: N761- Subacute and chronic vaginitis
Registration Number
CTRI/2022/01/039169
Lead Sponsor
Chettinad Hospital and Research Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All reproductive age women(18-39 years) with vaginal discharge and without any known gynaecological disorders.

Exclusion Criteria

Women with chronic inflammatory or autoimmune conditions

Women with poorly controlled Diabetes Mellitus

Women with sexually transmitted infections

Women currently on treatment with antimicrobials either topical or oral

Women on long term corticosteroids use

Women with contraceptives/ intrauterine devices

Pregnant women

Lactating mothers

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the effect of administering antimicrobials and probiotics in reproductive women with vaginal infectionTimepoint: Baseline, 2 weeks and 4 weeks
Secondary Outcome Measures
NameTimeMethod
To evaluate the reduction in the incidence of vaginal infectionsTimepoint: 2 weeks, 4 weeks
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