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Comparison of the vaginal tablet of vagiclean and metronidazole on Bacterial vaginosis

Comparison of the vaginal tablet of vagiclean and metronidazole on Bacterial vaginosis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220512054829N1
Enrollment
106
Registered
2022-09-19
Start date
2022-05-21
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Bacterial vaginosis. Inflammatory diseases of female pelvic organs

Interventions

Intervention 1: Intervention group: Vagiclean vaginal tablets. Intervention 2: Control group: Metronidazole vaginal tablets.

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: • Women in the age range of 18 to 49 years• Women who are sexually active• Bacterial vaginitis has been diagnosed in them.

Exclusion criteria

Exclusion criteria: • Pregnancy and lactation • The presence of an intrauterine device , Use of specific medications such as immunosuppressive drugs and broad-spectrum antibiotics • Having certain diseases such as liver, nerve, heart, kidney and blood dyscrasias and diabetes Use of antiprostaglandins • Complications from drug use or drug allergies • Vaginal candidiasis and Trichomonas vaginalis

Design outcomes

Primary

MeasureTime frame
Bacterial vaginitis. Timepoint: Before intervention, 5th days of intervention, 10th days of intervention. Method of measurement: Observation of symptoms.;Clinical symptoms (dysuria, itching, lower abdominal pain, burning, dysparonia, foul-smelling discharge, vaginal discharge). Timepoint: Before intervention, 5th days of intervention, 10th days of intervention. Method of measurement: Observation of symptoms.;Positive Amsel criteria (KOH test, PH test, clinical signs, smear test). Timepoint: Before intervention, 5th days of intervention, 10th days of intervention. Method of measurement: results of laboratory symptoms.

Secondary

MeasureTime frame
Dysuria, itching, lower abdominal pain, burning, dysparonia, foul-smelling discharge, vaginal discharge. Timepoint: Before intervention, 5th day of intervention, 10th day of intervention. Method of measurement: Clinical interview with the patient.;Positive Amsel criteria (KOH test, PH test, clinical signs, smear test). Timepoint: Before intervention, 5th day of intervention, 10th day of intervention. Method of measurement: Observation of symptoms.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Akbari

Kashan University of Medical Sciences

akbari1350_h@yahoo.com+98 31 5558 9057

Outcome results

None listed

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