Comparison · NCT00132691-sae
Flucinolone Acetonide Implant vs Systemic Therapy: 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. Flucinolone Acetonide Implant vs Systemic Therapy: serious adverse events. Trial comparisons, record NCT00132691-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00132691-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 | 0.581 | 0.495 | 0.663 | wilson | |
| Risk in group 2 | 0.373 | 0.294 | 0.46 | wilson | |
| Risk difference, group 1 minus group 2 | 0.208 | 0.0858 | 0.322 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.56 | 1.19 | 2.04 | log | |
| Odds ratio, group 1 over group 2 | 2.33 | 1.41 | 3.86 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Flucinolone Acetonide Implant than on Systemic Therapy | 4.8 | 3.1 | 11.7 | from the risk difference interval |
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 | Flucinolone Acetonide Implant | Participants randomized to receive implant therapy. | 75 | 129 | EG000 |
| Group 2 | Systemic Therapy | Participants randomized to receive systemic therapy. | 47 | 126 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 2 years
Source ClinicalTrials.gov
Trial
- Title
- Multicenter Uveitis Steroid Treatment (MUST) Trial
- NCT number
- NCT00132691
- Phases
- PHASE4
- Conditions
- Uveitis
- Interventions
- fluocinolone acetonide intraocular implant, oral corticosteroid with immunosuppressive agents as needed
- Lead sponsor
- JHSPH Center for Clinical Trials
- Results first posted
- 2012-07-30
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00132691?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.
For software
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GET https://conductscience.org/api/comparisons/v1/NCT00132691-sae