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Comparison · NCT00640835-sae

Buprenorphine/Naloxone Film Strip Administered Sublingually vs Buprenorphine/Naloxone Film Strip Administered Buccally: 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. Buprenorphine/Naloxone Film Strip Administered Sublingually vs Buprenorphine/Naloxone Film Strip Administered Buccally: serious adverse events. Trial comparisons, record NCT00640835-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00640835-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 10.02060.008050.0518wilson
Risk in group 20.01060.002920.038wilson
Risk difference, group 1 minus group 20.00998-0.02010.0421newcombe hybrid score
Risk ratio, group 1 over group 21.940.35910.5log
Odds ratio, group 1 over group 21.960.35410.8log
Number needed to harm, for one more participant with a serious adverse event on Buprenorphine/Naloxone Film Strip Administered Sublingually than on Buprenorphine/Naloxone Film Strip Administered Buccally
100from 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 1Buprenorphine/Naloxone Film Strip Administered Sublingually4194EG000
Group 2Buprenorphine/Naloxone Film Strip Administered Buccally2188EG001

Harm

What it counts
Total, serious adverse events
Time frame
12 weeks

Source ClinicalTrials.gov

Trial

Title
Safety and Tolerability of Buprenorphine/Naloxone Film Strips
NCT number
NCT00640835
Phases
PHASE2
Conditions
Opioid-Related Disorders
Interventions
Buprenorphine/naloxone Film Strip, Buprenorphine/naloxone Film Strip
Lead sponsor
Indivior Inc.
Results first posted
2010-10-26

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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