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A Comparison of Gentian Violet (GV) Mouth Washes, Nystatin, and Ketoconazole Tabs in Treating Oropharyngeal Candidiasis

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ClinicalTrials.gov Identifier: NCT00128323
Recruitment Status : Completed
First Posted : August 9, 2005
Last Update Posted : February 11, 2008
British Society for Antimicrobial Chemotherapy
Information provided by:
University of Malawi College of Medicine

Brief Summary:

In resource constrained societies and where HIV is a problem, oral thrush causes significant morbidity. In adults, ketoconazole is used and sometimes oral nystatin. Both drugs are relatively expensive compared to GV solution and ketoconazole has significant side effects especially in association with some of the treatments for HIV related problems.

In children, either GV solutions or nystatin are used, GV is a fraction of the cost of nystatin.

GV at 1% solution discolours the mouth (blue) and in the older child and adult would mark them out as having HIV infections. A much more dilute solution of GV has proved equally effective in vitro and would not carry the same cosmetic problem.

In this study of children, the investigators have compared the 3 solutions, 1% GV, 0.00165% GV and nystatin oral drops - all masked so that they look the same - to see if GV is more effective than nystatin, and to see if the weaker solution of GV is as effective as the stronger solution.

Condition or disease Intervention/treatment Phase
Candidiasis, Oral Drug: Gentian violet 1% solution Drug: Gentian violet 0.00165% solution Drug: Nystatin solution Phase 3

Detailed Description:

A double blind randomised trial of 2 strengths of GV solution and nystatin oral drops in the treatment of oropharyngeal candidiasis in children.

Children with oral thrush were enrolled from the paediatric wards of the Queen Elizabeth Central Hospital after permission and full information was given to the guardians.

Children of any age up to 14 years were included.

Mothers or guardians gave permission after pre counselling for HIV testing, and a saliva sample collection on enrollment. A full history and examination was carried out. The extent and severity of the candidal infection recorded on oral pictorial graphs and graded.

The child was then prescribed a treatment of A, B or C solution which was introduced into the mouth with a pipette. One ml of the solution was prescribed 3 times a day for 10 days.

The children were reviewed on day 3 to ensure no worsening of the condition and on day 12 when another saliva sample was taken.

A further review was carried out on day 21 of a limited number of children to repeat the saliva test.

Exclusions to the study were children who were already on an antifungal agent or those who had evidence of infection beyond the pharynx into the peritonsillar bed, suggesting the presence of oesophageal infection. These children were prescribed ketoconazole tabs.

If the oral infection was worse on day 3 miconazole gel was prescribed and the study medication stopped.

Sample size to achieve 80% power to detect a difference in failure rates of 20% and 10% (20% in the nystatin group and 10% in the GV groups) is 155 in each group.This assumes an HIV positivity of 50%. As a drop out rate of 20% is expected from death (in some HIV infected patients) or failure to attend for follow up, a sample size of 186 per group is to be recruited. This gives an overall number to be enrolled of 558 patients.

Recruitment has been completed - analysis is in progress.

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Study Type : Interventional  (Clinical Trial)
Enrollment : 558 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: A Comparison of Gentian Violet Mouth Washes, Nystatin Drops and Ketoconazole Tabs in the Treatment of Oropharyngeal Candidiasis
Study Start Date : November 2002
Actual Study Completion Date : April 2005

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Yeast Infections

Primary Outcome Measures :
  1. Clinical clearance of oral candidiasis by day 12
  2. Fungal clearance of oral candidiasis by saliva culture

Secondary Outcome Measures :
  1. Clinical and saliva fungal clearance in HIV infected and HIV uninfected children at 12 days and at 21 days

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Ages Eligible for Study:   up to 14 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • All children up to 14 years of age with proven oral candidiasis

Exclusion Criteria:

  • Children already on an antifungal agent or who had received an antifungal agent in the last week.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00128323

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Queen Elizabeth Central Hospital, Paediatric Dept, Box 360
Blantyre, Malawi, 3
Sponsors and Collaborators
University of Malawi College of Medicine
British Society for Antimicrobial Chemotherapy
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Principal Investigator: ELizabeth M Molyneux, FRCPCH FFAEM Malawi College of Medicine
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ClinicalTrials.gov Identifier: NCT00128323    
Other Study ID Numbers: P.01/02/130
BSAC Grant GA 532
First Posted: August 9, 2005    Key Record Dates
Last Update Posted: February 11, 2008
Last Verified: February 2008
Keywords provided by University of Malawi College of Medicine:
oropharyngeal candidiasis
GV solution
nystatin drops
Additional relevant MeSH terms:
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Candidiasis, Oral
Bacterial Infections and Mycoses
Mouth Diseases
Stomatognathic Diseases
Gentian Violet
Pharmaceutical Solutions
Anti-Bacterial Agents
Anti-Infective Agents
Antifungal Agents
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Anti-Infective Agents, Local