Comparison · NCT01453855-sae
Travoprost 0.003% vs TRAVATAN: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Travoprost 0.003% vs TRAVATAN: serious adverse events. Trial comparisons, record NCT01453855-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01453855-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0113 | 0.00484 | 0.0262 | wilson | |
| Risk in group 2 | 0.0166 | 0.00808 | 0.0339 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00531 | -0.0238 | 0.0119 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.68 | 0.218 | 2.13 | log | |
| Odds ratio, group 1 over group 2 | 0.677 | 0.213 | 2.15 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Travoprost 0.003% than on TRAVATAN | 188 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Travoprost 0.003% | Travoprost ophthalmic solution, 0.003%, one drop instilled in each eye, once daily, for three months | 5 | 442 | EG000 |
| Group 2 | TRAVATAN | Travoprost ophthalmic solution, 0.004%, one drop instilled in each eye, once daily, for three months | 7 | 421 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse events were collected from time of enrollment to study completion. An adverse event was considered to be any untoward medical occurrence in a patient exposed to the study medication.
Source ClinicalTrials.gov
Trial
- Title
- Travoprost 3-Month Safety and Efficacy Study
- NCT number
- NCT01453855
- Phases
- PHASE3
- Conditions
- Open-Angle Glaucoma, Ocular Hypertension
- Interventions
- Travoprost ophthalmic solution, 0.003%, Travoprost ophthalmic solution, 0.004%
- Lead sponsor
- Alcon Research
- Results first posted
- 2013-10-18
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01453855?tab=results
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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