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Comparison · NCT00390780-sae

Miconazole Lauriad Buccal Tablet vs Clotrimazole Troches: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Miconazole Lauriad Buccal Tablet vs Clotrimazole Troches: serious adverse events. Trial comparisons, record NCT00390780-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00390780-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.03450.01880.0623wilson
Risk in group 20.03140.01660.0585wilson
Risk difference, group 1 minus group 20.00312-0.02820.0346newcombe hybrid score
Risk ratio, group 1 over group 21.10.4542.67log
Odds ratio, group 1 over group 21.10.4422.76log
Number needed to harm, for one more participant with a serious adverse event on Miconazole Lauriad Buccal Tablet than on Clotrimazole Troches320from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Miconazole Lauriad Buccal TabletMiconazole Lauriad 50 mg mucoadhesive buccal tablet, once daily, for 14 days10290EG000
Group 2Clotrimazole TrochesClotrimazole troches, 10 mg, 5 times per day for 14 days9287EG001

Harm

What it counts
Total, serious adverse events
Time frame
14 days study treatment, then 21 days of follow-up

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety Study of Miconazole Lauriad to Treat Oropharyngeal Candidiasis in HIV Patients
NCT number
NCT00390780
Phases
PHASE3
Conditions
HIV Infections
Interventions
miconazole Lauriad, Clotrimazole
Lead sponsor
Valerio Therapeutics
Results first posted
2013-08-29

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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