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Comparison · NCT02252562-8125146c

Standard Practice vs Personal Hand Hygiene Device: Number of Participants With Postoperative Healthcare Acquired Infections

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

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

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ConductScience Library. Standard Practice vs Personal Hand Hygiene Device: Number of Participants With Postoperative Healthcare Acquired Infections. Trial comparisons, record NCT02252562-8125146c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02252562-8125146c

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Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.06670.05550.0799wilson
Risk in group 20.07090.05940.0844wilson
Risk difference, group 1 minus group 2-0.00424-0.02170.0132newcombe hybrid score
Risk ratio, group 1 over group 20.940.731.21log
Odds ratio, group 1 over group 20.9360.7131.23log
Number needed to treat, for one fewer participant with the outcome on Standard Practice than on Personal Hand Hygiene Device236from 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 1Standard PracticeUsual intraoperative hand hygiene (standard wall mounted devices and machine and/or cart based dispensers)1081,620OG000
Group 2Personal Hand Hygiene Device
Intraoperative use of personalized body worn alcohol dispensers incorporating a novel wireless tracking system \[(SAGE Products Inc., Cary, Il),~Sage Personal Hand Hygiene System: Utilization of a health care provider worn personal hand hygiene system during routine practice in the intra-operative setting with provider specific individual feedback.
1161,636OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Postoperative Healthcare Acquired Infections
Description
Patients with a prior infection and/or preexisting decolonization will be included and will be expected to be equally distributed between study groups given the randomized study design. For HCAI analysis, only new infection sites and/or a different organism of infection will be considered a new HCAI, per NHSN definitions.
Time frame
30-day after surgery
Population

Source ClinicalTrials.gov

Trial

Title
Hand Hygiene and Hospital Acquired Infections
NCT number
NCT02252562
Phases
NA
Conditions
Complication of Surgical Procedure
Interventions
Sage Personal Hand Hygiene System
Lead sponsor
Dartmouth-Hitchcock Medical Center
Results first posted
2019-02-18

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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