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Comparison of two vaginal cream Artemisia and clotrimazole in treatment of vaginal candidiasis

Comparison of two vaginal cream Artemisia kulbadica and clotrimazole in treatment of vaginal candidiasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121831454N1
Enrollment
60
Registered
2017-06-07
Start date
2017-02-18
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

vulvovaginit candidiasis. Vulvovaginal ulceration and inflammation in diseases classified elsewhere

Interventions

Intervention 1: Intervention group: treatment with vaginal cream 0/1% Artemisia- Built in the Pharmacy School of Mashhad University of Medical Sciences-one applicator every night for a week-Interventi
Treatment - Drugs
Intervention group: treatment with vaginal cream 0/1% Artemisia- Built in the Pharmacy School of Mashhad University of Medical Sciences-one applicator every night for a week-Intervention group
Control group: Treatment with vaginal cream Clotrimazole 1%- production of Aboreahan company-an applicator every night for a week-control group

Sponsors

Mashhad University of Medical Sciences - Deputy of Research and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: signs and symptoms of Candida vaginitis? positive culture and wet smear of vaginal discharge. Exclusion criteria: pregnancy? hypersensitivity to clotrimasol or artemisia? recurrent Candida vaginitis (4 or more Candida vaginitis in a year)? consumption of immunosuppressive drugs or systemic antibiotics? history of diabetes? using vaginal creams 2 weeks prior to the study? consumption of systemic anti-fungal drugs during 2 weeks prior to the study? presence of non-candidia vaginitis? consumption of oral contraceptives.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Discharge. Timepoint: Baseline, 1 week+_24 hours after treatment. Method of measurement: Clinical Examination, observation, and medical history.

Secondary

MeasureTime frame
Pruritus. Timepoint: Baseline, 1 week+_24hours after treatment. Method of measurement: History.;Erythema symptoma. Timepoint: Baseline, 1 week _+24 hours after treatment. Method of measurement: Observation, and History.;Dysuria. Timepoint: Baseline, 1 week+_24 hours after treatment. Method of measurement: History.;Dysparonia Symptom. Timepoint: Baseline, 1 week+_ 24hours after treatment. Method of measurement: History.;Vaginal Culture. Timepoint: Baseline, 1 week+_24 hours after treatment. Method of measurement: Vaginal Culture.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAla sabermahammad

School of Nursing and Midwifery

saberma921@mums.ac.ir+98 51 3750 3539

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026