ConductScience.org, home

Comparison · NCT00000125-sae

Observation vs Treatment: 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. Observation vs Treatment: serious adverse events. Trial comparisons, record NCT00000125-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00000125-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 10.01470.00840.0254wilson
Risk in group 20.01590.009320.027wilson
Risk difference, group 1 minus group 2-0.00126-0.0140.0114newcombe hybrid score
Risk ratio, group 1 over group 20.9210.4232.01log
Odds ratio, group 1 over group 20.920.4172.03log
Number needed to treat, for one fewer participant with a serious adverse event on Observation than on Treatment794from 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 1ObservationObservation only from February 1994 to June 2002 .12819EG000
Group 2TreatmentTopical Antiglaucoma Agents: Topical Antiglaucoma Agents from February 1994 to June 2002.13817EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events collected during OHTS I, from February 1994 to June 2002.

Source ClinicalTrials.gov

Trial

Title
Ocular Hypertension Treatment Study (OHTS)
NCT number
NCT00000125
Phases
PHASE3
Conditions
Ocular Hypertension, Glaucoma
Interventions
Topical ocular hypotensive eye drops.
Lead sponsor
Washington University School of Medicine
Results first posted
2015-03-19

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/NCT00000125-sae