ConductScience.org, home

Comparison · NCT00198133-sae

Thymoma vs Thymic Carcinoma: serious adverse events

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

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

Download JSON
Cite this record

ConductScience Library. Thymoma vs Thymic Carcinoma: serious adverse events. Trial comparisons, record NCT00198133-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00198133-sae

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1250.0350.36wilson
Risk in group 20.2730.09750.566wilson
Risk difference, group 1 minus group 2-0.148-0.4540.146newcombe hybrid score
Risk ratio, group 1 over group 20.4580.09112.31log
Odds ratio, group 1 over group 20.3810.05212.78log
Number needed to treat, for one fewer participant with a serious adverse event on Thymoma than on Thymic Carcinoma6.77from 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 1ThymomaPatients with Thymoma who received Pemetrexed 500 mg/m2 IV every 3 weeks216EG000
Group 2Thymic CarcinomaPatients with Thymic Carcinoma who received Pemetrexed 500 mg/m2 IV every 3 weeks311EG001

Harm

What it counts
Total, serious adverse events
Time frame
Beginning of treatment until the end of the study, up to 3 years

Source ClinicalTrials.gov

Trial

Title
Phase II Study of Alimta (Pemetrexed) Treatment of Advanced Thymoma and Thymic Carcinoma
NCT number
NCT00198133
Phases
PHASE2
Conditions
Thymoma, Thymic Carcinoma
Interventions
Premetrexed (Alimta)
Lead sponsor
Patrick Joseph Loehrer Sr.
Results first posted
2016-01-25

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT00198133-sae