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The effect of tinidazole for treatment and recurrence of bacterial vaginosis

Clinical trial of comparison the effect of tinidazole and metronidazole tablet for treatment and recurrence of bacterial vaginosis in women of reproductive age

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012073110457N1
Enrollment
110
Registered
2013-03-20
Start date
2012-09-22
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

Bacterial vaginosis. Acute vaginitis

Interventions

Intervention 1: Intervention 1, Tinidazole, oral tablet, 2 g daily for two day,brand name:Tindamax, Manufacturer:Kimidaru. Intervention 2: Intervention 2, Metronidazole, oral tablet, 500 mg, twice da
Treatment - Drugs
Intervention 1, Tinidazole, oral tablet, 2 g daily for two day,brand name:Tindamax, Manufacturer:Kimidaru
Intervention 2, Metronidazole, oral tablet, 500 mg, twice daily for seven day, brand name: Metromax , Manufacturer:kimidaru

Sponsors

Vice chancellor for research, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 45-15 years, married women, diagnosis of bacterial vaginosis by clinical signs and diagnostic tests, accept the use of condoms during treatment. Exclusion criteria: associated with Candida vaginitis and trichomonas, Pregnancy, consume antibiotics at the same time or within two weeks and using the vaginal cream, metronidazole used simultaneously to any cause, having a chronic disease and diabetes, Immunosuppression or immune-lowering medication use, having cervicitis, chronic bacterial vaginosis

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Vaginal discharge. Timepoint: Pre intervention, two and four weeks after treatment. Method of measurement: Observation.;Vaginal PH. Timepoint: Pre intervention.two and four weeks after treatment. Method of measurement: Universal indicator paper.;Wiff test. Timepoint: Pre intervention,two and four weeks after treatment. Method of measurement: KOH.;Clue cell. Timepoint: Pre intervention, two and four weeks after treatment. Method of measurement: Pap smear.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZeinab Rabee

Ahvaz Jundishapur University of Medical Sciences

rabee@ajums.ac.ir+98 77 2722 3203

Outcome results

None listed

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