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The comparative of Poulk vaginal gel and metronidazole vaginal gel effect on treatment of bacterial vaginosis

Phase 2
Not yet recruiting
Conditions
Bacterial Vaginosis.
Other specified inflammation of vagina and vulva
N76.7
Registration Number
IRCT20201201049560N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
112
Inclusion Criteria

willingness to cooperate
positive Whiff test
signs of bacterial vaginosis in examination
Positive cluecell

Exclusion Criteria

Multi partner
Stricken to specific diseases like liver diseases ,kidney diseases and central chords system diseases ,blood dyscrasi ,diabetes ,impair of safety system
Having abnormal uterus bleeding
Frequently vulvovaginits
pregnancy
Mensturation
Lactating
Use of vaginal douches frequently, consuming remedy for treatment in 3 recent months
Consumig alcohol and anti coagulation remedies and recent consuming anti-parasite remedy, anti-biotic, weakening remedy of safety system and vaginalis remedy
President of allergy in using metronidazol tablet
consuming remedy for treatment in 3 recent months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bacterial Vaginosis. Timepoint: Before treatment and after treatment. Method of measurement: Based on the criteria of Amsell (Evaluation of vaginal discharge in terms of odor, color and presence of key cells with the emphasis on emphasis) and Nugent.
Secondary Outcome Measures
NameTimeMethod
Vaginal discharge. Timepoint: 14-28 days after treatment. Method of measurement: Observation.;The acidity of vagina. Timepoint: 14-28 days after treatment. Method of measurement: PH strip.;Whiff test. Timepoint: 14-28 days after treatment. Method of measurement: Potassium hydroxide solution 10%.;Clue cells. Timepoint: 14-28 days after treatment. Method of measurement: Evaluation of clue cells on the wet lam.;Sexual Fanction score. Timepoint: Before and 14 days after treatment. Method of measurement: Rosen Sexual Function Questionnaire.;Sexual Satisfaction score. Timepoint: Before and 14 days after treatment. Method of measurement: Larson Sexual Satisfaction Questionnaire.
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