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
| Type | Name | Description |
|---|---|---|
| DRUG | Tinidazole 56 | Tinidazole , 2g, twice daily for 14 days. At the same time, metronidazole, 400 mg, once a day, vaginal administration, 14 days. |
| DRUG | Tinidazole 42 | Tinidazole , 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.