Trichomonas Vaginitis Clinical Trial
Official title:
Oral Tinidazole Treatment of Refractory Trichomonas Vaginitis
We compare two oral tinidazole regimens for refractory trichomonas vaginitis.
Status | Not yet recruiting |
Enrollment | 20 |
Est. completion date | December 30, 2025 |
Est. primary completion date | December 30, 2025 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 55 Years |
Eligibility | Inclusion Criteria: - Women be at least 18 years of age - Failure of conventional treatment (recommended by guidelines including tinidazole, 2g once daily for 5-7 days) Exclusion Criteria: - Allergy to metronidazole or tinidazol - Pregnant or nursing - HIV or other chronic disease |
Country | Name | City | State |
---|---|---|---|
China | Beijing Obstetrics and Gynecology Hospital,Capital Medical University | Peking | |
China | Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University | Peking | |
China | Peking University First Hospital | Peking | |
China | Peking University Shenzhen Hospital | Shenzhen | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Shangrong Fan |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cure rate of refractory trichomoniasis | Evaluate the efficacy of oral tinidazole tablets in the treatment of refractory trichomoniasis.Diagnosis of vaginal trichomoniasis is performed by microscopy of vaginal secretions. Cure or failure was based on positive or negative T. vaginalis on vaginal secretions by microscopy examination. | 24 weeks | |
Secondary | Safety of tinidazole tablets | Number of participants with treatment-related adverse events as assessed by CTCAE v4.0. Test of blood routine,liver function, kidney function ,and urine routine will be done before treatment.The same test will be were reviewed within 1 week after treatment. | 24 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00213018 -
Safety, Acceptability and Preliminary Effectiveness of Carraguard™ (PC-515) in Preventing HIV/STI Transmission
|
Phase 2 | |
Completed |
NCT01874158 -
DNA Clearance of Uncomplicated Trichomonas Vaginalis Infections in HIV Negative Women
|
Phase 4 | |
Completed |
NCT00978848 -
Non-Invasive Sexually Transmitted Disease Testing in Women Seeking Emergency Contraception or Urine Pregnancy Testing
|
N/A | |
Active, not recruiting |
NCT06131749 -
Genital Tract Infections, the Vaginal Microbiome and Gestational Age at Birth Among Pregnant Women in South Africa
|
||
Completed |
NCT03090802 -
MAMAS: Mentoring Adolescent Mothers at School
|
N/A | |
Not yet recruiting |
NCT06438575 -
Point of Care Diagnosis of Vaginal Infections
|
N/A | |
Completed |
NCT00213057 -
Safety and Acceptability of Carraguard™ Among HIV-negative Couples in Thailand
|
Phase 1 | |
Not yet recruiting |
NCT06261840 -
Refining Treatment Options for Trichomonas Vaginalis Infection: A Comparative Analysis of Metronidazole and Secnidazole
|
Phase 4 | |
Completed |
NCT00140764 -
Intravaginal Treatment of Disturbances of Vaginal Flora Among HIV Infected and Uninfected Women in Malawi
|
Phase 3 | |
Completed |
NCT00213031 -
Safety, Acceptability and Preliminary Effectiveness of PC-515 for Vaginal Use as a Possible Microbicide
|
Phase 2 | |
Active, not recruiting |
NCT05666778 -
Single Arm Trial of Menstrual Cups Among Economically Vulnerable Women to Reduce Bacterial Vaginosis and STIs
|
Phase 2 | |
Completed |
NCT01361048 -
Neo-Penotran Forte Vaginal Suppository for Vaginal Trichomoniasis
|
Phase 2 | |
Completed |
NCT04189744 -
The ASPIRE Trial - Aiming for Safe Pregnancies by Reducing Malaria and Infections of the Reproductive Tract
|
Phase 3 | |
Recruiting |
NCT04219605 -
Evaluation of a Rapid Microscopic Diagnostic System for Different Vaginitis Conditions
|