Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT05383521

Safety and Efficacy of Two Oral Tinidazole Regimens for Refractory Trichomonas Vaginitis

Oral Tinidazole Treatment of Refractory Trichomonas Vaginitis

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Shangrong Fan · Academic / Other
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

We compare two oral tinidazole regimens for refractory trichomonas vaginitis.

Detailed description

Refractory trichomonas vaginitis has become a clinical problem, which has a direct impact on the health and life of patients. Refractory trichomonas vaginitis is mainly caused by drug resistance of trichomonas. Drug resistant trichomonas has appeared China. Increasing the dosage of anti trichomonal drugs is the main treatment method at present. The aim of this study was to evaluate the efficacy and safety of two oral tinidazole regimens for refractory trichomonas vaginitis.

Conditions

Interventions

TypeNameDescription
DRUGTinidazole 56Tinidazole , 2g, twice daily for 14 days. At the same time, metronidazole, 400 mg, once a day, vaginal administration, 14 days.
DRUGTinidazole 42Tinidazole , 1g, three times daily for 14 days. At the same time, metronidazole, 400 mg, once a day, vaginal administration, 14 days.

Timeline

Start date
2025-12-01
Primary completion
2025-12-30
Completion
2025-12-30
First posted
2022-05-20
Last updated
2024-06-11

Locations

4 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05383521. Inclusion in this directory is not an endorsement.