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The effect of vaginal products on the basis of traditional medicine in Vaginitis

The effect of vaginal preparation on the basis of traditional medicine (containing masoids and zeinans) on the recovery and relapse of bacterial vaginitis and trichomoniasis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180217038764N2
Enrollment
40
Registered
2019-08-24
Start date
2018-09-12
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Bacterial vaginitis and Trichomoniasis. Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere

Interventions

Intervention 1: "Intervention group": use of traditional medicine (including masoids and zeinans) vaginal suppository 10%, for 7 days, Each day one vaginal suppository (total of 7 vaginal suppositor

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: patient satisfaction Age 18-50 years Symptoms of bacterial Vaginosis and Trichomoniasis in clinical examinations and tests

Exclusion criteria

Exclusion criteria: Recent use of anti-parasitic drugs, antibiotics, immunosuppressive drugs and vaginal drugs over the past two weeks Intercourse and using vaginal shower for the last 48 hours Abnormal uterine bleeding Pregnancy and non-Lactation Use of vaginal shower repeatedly Smoking and alcohol consumption and coumarin anticoagulants Multiplicity of sex partners studied Cases of certain diseases such as liver disease, central nervous system diseases,Blood disorders, diabetes, immune deficiency and sexually transmitted diseases having allergy to the medication compounds used in the study.

Design outcomes

Primary

MeasureTime frame
Improvement of symptoms of bacterial vaginitis and trichomoniasis. Timepoint: First follow up 10 days after intervention, Second follow up four weeks after intervention, Third follow up three months after intervention. Method of measurement: Questionnaire, examination, test.

Secondary

MeasureTime frame
Improvement of the recurrence of bacterial vaginitis and trichomoniasis. Timepoint: First follow up 10 days after intervention, Second follow up four weeks after intervention, Third follow up three months after intervention. Method of measurement: Questionnaire, examination, test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojgan Tansaz

Shahid Beheshti University of Medical Sciences

tansaz_mojgan@sbmu.ac.ir+98 21 8877 3521

Outcome results

None listed

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