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Comparison · NCT00807989-4ebcee35

Carbamazepine vs Lamotrigine/Valproate: Seizure Free Rate for 52 Weeks at Initial Target Dose

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. Carbamazepine vs Lamotrigine/Valproate: Seizure Free Rate for 52 Weeks at Initial Target Dose. Trial comparisons, record NCT00807989-4ebcee35. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00807989-4ebcee35

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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 10.4780.3780.58wilson
Risk in group 20.6410.530.739wilson
Risk difference, group 1 minus group 2-0.163-0.303-0.0127newcombe hybrid score
Risk ratio, group 1 over group 20.7450.5680.979log
Odds ratio, group 1 over group 20.5120.2750.953log
Number needed to treat, for one fewer participant with the outcome on Carbamazepine than on Lamotrigine/Valproate6.133.378.8from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CarbamazepineCarbamazepine~Carbamazepine4390OG000
Group 2Lamotrigine/ValproateLamotrigine and Valproate combination therapy~Lamotrigine/Valproate5078OG001

Outcome

Type
SECONDARY
Title
Seizure Free Rate for 52 Weeks at Initial Target Dose
Description
Time frame
52 weeks
Population

Source ClinicalTrials.gov

Trial

Title
The Efficacy and Safety of Low Dose Combination of LTG and VPA Compared to CBZ Monotherapy
NCT number
NCT00807989
Phases
PHASE4
Conditions
Epilepsy
Interventions
Carbamazepine, Lamotrigine/Valproate
Lead sponsor
Yonsei University
Results first posted
2015-05-29

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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