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Study of the Management of Vaginal Discharge in West African Using Single Dose Treatments
This study has been completed.
Sponsors and Collaborators: Universitaire de Sherbrooke
Canadian International Development Agency
Information provided by: Universitaire de Sherbrooke
ClinicalTrials.gov Identifier: NCT00313131
  Purpose

This randomised controlled trial aimed to verify whether directly observed single dose treatment (with tinidazole+fluconazole) would be as effective as the longer standard treatments (metronidazole for 7 days, plus vaginal clotrimazole for 3 days) in the syndromic management of women presenting with vaginal discharge in primary health care centers of Ghana, Togo, Guinea and Mali. It was designed as an effectiveness trial, i.e. it was done under conditions typical of routine work in these health centers


Condition Intervention Phase
Bacterial Vaginosis
Candidiasis
Vaginitis
Drug: tinidazole+fluconazole vs metronidazole+clotrimazole
Phase III

MedlinePlus related topics: Yeast Infections
Drug Information available for: Metronidazole Metronidazole hydrochloride Metronidazole phosphate Clotrimazole Miconazole Miconazole nitrate Tioconazole Fluconazole Tinidazole
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: A Randomised Controlled Trial of Single Dose Tinidazole+Fluconazole Versus Longer Courses of Metronidazole+Clotrimazole in the Management of West African Women With Vaginal Discharge

Further study details as provided by Universitaire de Sherbrooke:

Primary Outcome Measures:
  • Symptomatic resolution of the vaginal discharge according to the patient

Secondary Outcome Measures:
  • Objective resolution of the vaginal discharge according to the study nurse or medical officer

Estimated Enrollment: 1524
Study Start Date: January 2004
Estimated Study Completion Date: May 2005
Detailed Description:

Abstract Objective: Evaluate whether single-dose treatments are as effective as standard therapy in the syndromic management of vaginal discharge.

Methods: A randomized controlled effectiveness trial comparing single-dose tinidazole plus fluconazole (TF) to seven days of metronidazole plus three days of vaginal clotrimazole (MC) among 1570 women presenting with vaginal discharge in primary health care institutions of Ghana, Togo, Guinea and Mali. Participants were randomly allocated to one of the two treatments by research nurses or physicians using pre-coded envelopes. Effectiveness was assessed by symptomatic response on day 14.

Findings: The two treatment regimens had similar effectiveness: complete resolution was seen in 66% (TF) and 64% (MC) and partial resolution in 33% (TF) and 34% (MC) of participants (p=0.26). Effectiveness was similar among subgroups with vulvovaginal candidiasis, T. vaginalis vaginitis or bacterial vaginosis. The two treatment regimens had a similar effectiveness among HIV-infected (TF: n=76, 71% complete resolution, 28% partial; MC: n=83, 72% complete, 25% partial, p=0.76) and HIV-uninfected women (TF: n=517, 68% complete, 32% partial; MC: n=466, 65% complete, 33% partial, p=0.20). Cervical infections with N. gonorrhoeae, C. trachomatis and M. genitalium were uncommon among women not involved in sex work, were associated with bacterial vaginosis or T. vaginalis vaginitis, and did not alter response to treatment with agents active against vaginal infections. Four fifths of women not relieved by single-dose TF had a favourable response when MC was administered as second-line treatment.

Conclusion: Single-dose TF is as effective as multiple-dose MC in the syndromic management of vaginal discharge, even among the HIV-infected. Given its low price and easier compliance, tinidazole/fluconazole should be considered as a first-line treatment of the vaginal discharge syndrome.

  Eligibility

Ages Eligible for Study:   11 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • women consulting for vaginal discharge
  • local resident
  • willingness and ability to consent

Exclusion Criteria:

  • sex worker consulting for active screening
  • main complaint of lower abdominal pain
  • allergy to one of the study drugs
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00313131

Locations
Ghana
Adabraka Polyclinic
Accra, Ghana
Suntreso Polyclinc
Kumasi, Ghana
Guinea
Centre de Santé Madina
Conakry, Guinea
Centre de Santé Carrière
Conakry, Guinea
Togo
Clinique IST d'Amoutivé
Lomé, Togo
Clinique IST d'Agoe Nyivé
Lomé, Togo
Centre de Santé d'Adakpamé
Adakpame, Togo
Sponsors and Collaborators
Universitaire de Sherbrooke
Canadian International Development Agency
Investigators
Principal Investigator: Jacques Pepin, MD U of Sherbrooke
  More Information

Publications indexed to this study:
Study ID Numbers: CHUS 03-32
Study First Received: April 7, 2006
Last Updated: April 7, 2006
ClinicalTrials.gov Identifier: NCT00313131  
Health Authority: Canada: Health Canada

Keywords provided by Universitaire de Sherbrooke:
bacterial vaginosis
vaginal candidiasis
trichomoniasis
vaginitis
Ghana
Togo
Mali
Guinea

Study placed in the following topic categories:
Fluconazole
Bacterial Infections
Metronidazole
Candidiasis
Vaginal Discharge
Clotrimazole
Miconazole
Vaginitis
Trichomonas Infections
Tioconazole
Vaginal Diseases
Genital Diseases, Female
Mycoses
Vaginosis, Bacterial
Tinidazole

Additional relevant MeSH terms:
Anti-Infective Agents
Anti-Infective Agents, Local
Antiparasitic Agents
Antiprotozoal Agents
Molecular Mechanisms of Pharmacological Action
Radiation-Sensitizing Agents
Antifungal Agents
Therapeutic Uses
Physiological Effects of Drugs
Antitrichomonal Agents
Alkylating Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009