Gentian Violet Vs. Nystatin Oral Suspension for Treatment of Oropharyngeal Candidiasis
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| ClinicalTrials.gov Identifier: NCT01427738 |
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Recruitment Status
:
Completed
First Posted
: September 2, 2011
Results First Posted
: February 16, 2015
Last Update Posted
: February 16, 2015
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Sponsor:
AIDS Clinical Trials Group
Collaborator:
National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by (Responsible Party):
AIDS Clinical Trials Group
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Brief Summary:
The purpose of this study was to see which one of two medicines (topical gentian violet [GV] or nystatin oral suspension) was better than the other in treating Oral Candidiasis (OC). This was measured by whether the study participant still had OC or sores in his/her mouth after 14 days of treatment. Also, safety and tolerability of GV and nystatin in the treatment of OC were assessed.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| HIV-1 Infection | Drug: Gentian Violet Drug: Nystatin oral suspension | Phase 3 |
A5265 was a phase III, open-label (both the researchers and participants know which treatment was being administered) clinical trial to compare the safety and efficacy of topical GV to that of oral nystatin suspension. Male and female HIV-1 positive participants ≥ 18 years of age were randomized (as if by the toss of a coin) with equal probability and stratified by CD4+ T-cell counts and the use of antiretroviral therapy at the time of study entry to receive either topical GV solution (5 mL swish and gargle for 1 minute and spit two times daily) or nystatin oral suspension (5 mL swish for 1 minute and swallow four times daily) for 14 days. Therapy was considered as failed if participants have no clinical improvement (assessed by severity of pseudomembranous candidiasis) during either treatment regimen. Evaluation of signs and symptoms of oral candidiasis was done by an evaluator who was blinded to the treatment assignment. A total of 494 participants was expected to enroll in the study but due to early study closure only 221 enrolled; and participants are expected to be on the study for about 13 weeks.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 221 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | A Phase III, Open-Label, Randomized, Assessment-Blinded Clinical Trial to Compare the Safety and Efficacy of Gentian Violet Oral Solution to That of Nystatin Oral Suspension for the Treatment of Oropharyngeal Candidiasis in HIV-1 Infected Participants in Non-U.S. Settings |
| Study Start Date : | June 2011 |
| Actual Primary Completion Date : | September 2012 |
| Actual Study Completion Date : | January 2014 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Arm A: Topical GV solution
Topical GV 0.00165% solution (5 mL swish and gargle for 1 minute and expectorate [spit] 2 times per day [BID]) for 14 days
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Drug: Gentian Violet
Participants were administered topical Gentian violet solution, orally, twice daily for 14 days.
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Active Comparator: Arm B: Nystatin oral suspension
Nystatin oral suspension (5 mL of 100,000 units/mL swish for 1 minute and swallow 4 times per day [QID]) for 14 days
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Drug: Nystatin oral suspension
Participants were administered Nystatin oral suspension 4 times a day for 14 days.
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Primary Outcome Measures
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- Number of Participants With Clinical Efficacy [ Time Frame: After 14 days of treatment ]The primary endpoint is clinical efficacy defined as cure (absence of lesions) or improvement (a decrease in severity of lesions) after 14 days of treatment. The oral cavity will be split arbitrarily into 6 sites: left lower and upper labial mucosa and buccal mucosa, right lower and upper labial mucosa and buccal mucosa, hard palate, soft palate, tongue (dorsum, lateral, and ventral), and floor of mouth. Severity is scored using a scoring system from 0 to 3 (0 corresponds to absence of lesions, and 3 corresponds to presence of extensive confluent lesions) which leads to a composite severity score ranging from 0 to 18 after adding up the scores from all 6 sites. Complete success is assigned if the composite score after treatment equals to 0. Improved/partial response is assigned if the composite score after treatment is less than the baseline score. The blinded evaluator scores the severity of lesions by examining different lesion characteristics.
Secondary Outcome Measures
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- Number of Participant With Symptom [ Time Frame: after 14 days of treatment ]Symptoms were assessed using a visual analog scale where the level of discomfort and pain were recorded and quantified using a scoring system from 0 to 3. 0=no discomfort/pain; 1=mild discomfort/pain; 2=Moderate discomfort/pain; 3=Severe discomfort/pain.
- Quantitative Yeast Colony Counts [ Time Frame: At weeks 0, 2, 6 ]If quantitative yeast culture yielding < 20 CFU/mL of Candida spp., then we call this mycological success
- Tolerance [ Time Frame: After 14 days of treatment ]The investigators will measure tolerance using a scale from 0 to 3 (0=No side effects experienced, no changes in treatment; 1=Some side effects experienced, but not enough to modify treatment; 2=Some side effects experienced, resulted in treatment interruption; 3=Side effects experienced, resulted in treatment discontinuation.)
- Number of Participants Who Were Adherent. [ Time Frame: After 14 days of treatment ]Adherence was reported as a dichotomous variable (adherence vs. non-adherence). Participants who have missing doses less than 15% will be considered as adherent, i.e., if a participant is in the GV arm, then the cutoff point is 28*0.15=4 doses; and for the nystatin arm is 56*0.15=8 doses.
- Self-Assessment of General Health [ Time Frame: Weeks 0, 6 ]Participants rated their general health on two scales. One is a five point scale ranging from 1 to 5 (1=Excellent; 2=Very Good; 3=Good; 4=Fair; 5=Poor)
- Number of Participants Who Found GV and Nystatin Acceptable. [ Time Frame: After 14 days of treatment ]Acceptability was defined as the willingness to use the drug if it is proven effective to treat oral candidiasis. Participants were asked whether or not they would be willing to use the assigned treatment via questionnaires.
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| Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- HIV-1 infection, documented by any licensed rapid HIV test or HIV enzyme or chemiluminescence immunoassay (E/CIA) test kit at any time prior to study entry and confirmed by licensed Western blot or a second antibody test by a method other than the initial rapid HIV and/or E/CIA, or by HIV-1 antigen, plasma HIV-1 RNA viral load.
- Pseudomembranous candidiasis documented by a complete oral exam (i.e., white or yellow spots or plaques with an underlying erythematous base, located in any part of the oral cavity) at the screening visit. Participants with documented angular chelitis and/or erythematous candidiasis without pseudomembranous candidiasis were not eligible to enroll in the study.
- If on an antiretroviral therapy (ART), initiation of regimen at least 12 weeks prior to study entry, and willingness of participant to remain on current ART regimen until the study-defined 14-day treatment period was complete. NOTE: Participants who were not ART-naïve and not on ART were eligible to participate in the study if they did not intend to initiate ART during the study- defined 14-day treatment period.
- CD4+ cell count obtained within 30 days prior to study entry at a DAIDS-approved laboratory.
Exclusion Criteria:
- Documented or presumptive signs or symptoms of esophageal candidiasis (e.g., dysphagia) during the screening period unless endoscopic examination of the esophagus was performed, and fungal esophagitis were excluded.
- Use of any investigational drug currently or within 30 days prior to study entry. NOTE: For purposes of this study, drugs available under an FDA-authorized expanded access program was NOT considered investigational.
- Concurrent vaginal candidiasis within 21 days prior to study entry.
- Use of inhaled or systemic corticosteroids within 14 days prior to study entry.
- Use of any antifungal agents within 30 days prior to study entry.
- Anticipated need for systemic or oral/topical antifungal agents for other diagnoses within the study-defined 14-day treatment period.
- Intend to initiate ART during the screening period, at study entry, or within the study-defined 14-day treatment period.
- Intend to use any additional oral topical treatments within the study- defined 14-day treatment period.
- Known allergy/sensitivity or any hypersensitivity to components of study drugs or their formulation.
- Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
- Serious illness, in the opinion of the site investigator, requiring systemic treatment.
- Hospitalization within 30 days prior to study entry for HIV or HIV-related conditions.
- Previous or current history of porphyria.
- Presence of oral warts during the screening period or at the study entry visit before randomization.
- Current wearing of full dentures or a maxillary partial denture at study entry
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): NCT01427738
Locations
| Botswana | |
| Gaborone Prevention/Treatment Trials CRS (12701) | |
| Gaborone, Botswana | |
| Molepolole Prevention/Treatment Trials CRS (12702) | |
| Molepolole, Botswana | |
| India | |
| BJ Medical College CRS (31441) | |
| Pune, Maharashtra, India, 411001 | |
| National AIDS Research Institute Pune CRS (11601) | |
| Pune, Maharashtra, India, 411026 | |
| Kenya | |
| AMPATH at Moi Univ. Teaching Hosp. Eldoret CRS (12601) | |
| Eldoret, Kenya, 30100 | |
| Walter Reed Project - Kenya Med. Research Institute Kericho CRS (12501) | |
| Kericho, Kenya, 20200 | |
| Malawi | |
| College of Med. JHU CRS (30301) | |
| Blantyre, Malawi | |
| South Africa | |
| Durban Adult HIV CRS (11201) | |
| Durban, South Africa, 4013 SF | |
| Uganda | |
| Joint Clinical Research Centre (JCRC) (12401) | |
| Kampala, Uganda | |
| Zimbabwe | |
| UZ-Parirenyatwa CRS (30313) | |
| Harare, Zimbabwe | |
Sponsors and Collaborators
AIDS Clinical Trials Group
National Institute of Allergy and Infectious Diseases (NIAID)
Investigators
| Study Chair: | Robert A Salata, MD | Case CRS | |
| Principal Investigator: | James G Hakim, MD | UZ- Parirenyatwa CRS | |
| Principal Investigator: | Tim Hodgson, MD | Eastman Dental Hospital | |
| Principal Investigator: | Richard J Jurevic, DDS, PhD | Case CRS | |
| Principal Investigator: | Pranab K Mukherjee, PhD, MSc | Case CRS | |
| Principal Investigator: | Cissy M Kityo, MBChB, MSc | JCRC CRS | |
| Principal Investigator: | Rana Traboulsi, MD | Case CRS | |
| Principal Investigator: | Srikanth P Tripathy, MD, MBBS | NARI Pune CRS | |
| Principal Investigator: | Mahmoud A Ghannoum, Phd, MSc | Case Western Reserve University |
| Responsible Party: | AIDS Clinical Trials Group |
| ClinicalTrials.gov Identifier: | NCT01427738 History of Changes |
| Obsolete Identifiers: | NCT01494129 |
| Other Study ID Numbers: |
ACTG A5265 1U01AI068636 ( U.S. NIH Grant/Contract ) |
| First Posted: | September 2, 2011 Key Record Dates |
| Results First Posted: | February 16, 2015 |
| Last Update Posted: | February 16, 2015 |
| Last Verified: | February 2015 |
Additional relevant MeSH terms:
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Candidiasis Mycoses Pharmaceutical Solutions Nystatin Gentian Violet Anti-Bacterial Agents |
Anti-Infective Agents Antifungal Agents Ionophores Membrane Transport Modulators Molecular Mechanisms of Pharmacological Action Anti-Infective Agents, Local |