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Comparison of the effect of Harpagophytum procumbens and topical Hydrocortisone in improving genital skin inflammation in patients with candidiasis

Phase 3
Conditions
Candidal vulvovaginitis.
Candidiasis of vulva and vagina
B37.3
Registration Number
IRCT20210508051222N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
60
Inclusion Criteria

Having an age range of fifteen to fifty years
Being married
Signs and symptoms of candidate vaginitis in the interview

Exclusion Criteria

Use of broad-spectrum antibiotics in the last two weeks
Use of oral and vaginal medications related to the treatment of genital infections during the last two weeks
Any allergies to the drug compounds used in the research
Trichomonas vaginitis

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The amount of burning of external genitalia. Timepoint: Before the start of the study and 7 days after taking the drug. Method of measurement: 5-points checklist.;The amount of itching of external genitalia. Timepoint: Before the start of the study and 7 days after taking the drug. Method of measurement: 5-points checklist.;Amount of redness and swelling of the external genitalia. Timepoint: Before the start of the study and 7 days after taking the drug. Method of measurement: 5-points checklist.
Secondary Outcome Measures
NameTimeMethod
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