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Comparison short period of time fluconazole-oral protexin and fluconazole complex in treatment of Vulvovaginal Candidiasis

English:Comparison short period of time fluconazole-oral protexin and fluconazole complex in treatment of Vulvovaginal Candidiasis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201106206807N3
Enrollment
90
Registered
2012-05-13
Start date
2011-10-09
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

Vulvovaginal Candidiasis. Vaginitis, vulvitis and vulvovaginitis in infectious and parasitic diseases classified elsewhere

Interventions

Sponsors

The International Branch of Shahid Beheshti University of Medical Sciences & Health Services
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:1-Married women aged 18-40 years 2-Having one partner 3-Absence of pregnancy and breast feeding 4-Absence of mensturation at the time of attendance 5-Useage of the clotrimazole for a temporary time and lack of improvement-6-Not using vaginal drug, antibiotics , immonosupressive drugs and exogenous hormones such as oral contraceptives since 2 weeks before starting the research 7-Not having intercourse or using vaginal douche within the last 24 hours 8-Absence of other types of trichmonas vaginitis and bacterial vaginosis at the time of study 9- Absence of any diagnose medical disease such as diabetis and other auto immune diseases , by asking a patient 10-Verification of vulvovaginal Candidiasis resalted clinical symptoms and KOH positive examples and cultivation. Exclusion criteria: 1-Allergic reactions of fluconazole and protexin 2-Pregnancy during therapy 3-Compulsion to use antibiotics or other anti fungous medicines 4-The menses 5-Usage of vaginal douche during treatment 6-Sexual intercourse without condoms during treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Volvovaginitis Candidiasis. Timepoint: At the time of presentation and 5-7 days after treatment. Method of measurement: Observation- Sabouraud dextrose agar medium.

Secondary

MeasureTime frame
Volvovaginitis Candidiasis treatment. Timepoint: 5-7 days after treatment. Method of measurement: Observations-Sabouraud dextrose agar medium.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoheila Nouraei

The International Branch of Shahid Beheshti University of Medical Sciences & Health Services

Soheilanouraei@yahoo.com+98 21 2226 5994

Outcome results

None listed

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