ConductScience.org, home

Comparison · NCT01429441-sae

Ocriplasmin vs Sham: 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. Ocriplasmin vs Sham: serious adverse events. Trial comparisons, record NCT01429441-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01429441-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 10.3360.2640.416wilson
Risk in group 20.3650.2640.479wilson
Risk difference, group 1 minus group 2-0.0292-0.1640.0992newcombe hybrid score
Risk ratio, group 1 over group 20.920.6311.34log
Odds ratio, group 1 over group 20.8790.491.58log
Number needed to treat, for one fewer participant with a serious adverse event on Ocriplasmin than on Sham34.2from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: sham.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1OcriplasminSubjects in the ocriplasmin group received a single intravitreal injection of ocriplasmin 0.125mg49146EG000
Group 2ShamSubjects in the sham group received a single sham injection2774EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were collected from the injection day (Day 0) up to discontinuation from the study or completion of the study (Month 24).

Source ClinicalTrials.gov

Trial

Title
Ocriplasmin for Treatment for Symptomatic Vitreomacular Adhesion Including Macular Hole
NCT number
NCT01429441
Phases
PHASE3
Conditions
Vitreomacular Adhesion Including Macular Hole
Interventions
Ocriplasmin, Sham injection
Lead sponsor
ThromboGenics
Results first posted
2016-01-11

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.govNone 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/NCT01429441-sae