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Comparison · NCT04756804-sae

70% Isopropyl Alcohol Novel Preoperative Skin Antiseptic vs 2% Chlorhexidine Gluconate/70% Isopropyl Alcohol Preoperative Skin Antiseptic: serious adverse events

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. 70% Isopropyl Alcohol Novel Preoperative Skin Antiseptic vs 2% Chlorhexidine Gluconate/70% Isopropyl Alcohol Preoperative Skin Antiseptic: serious adverse events. Trial comparisons, record NCT04756804-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04756804-sae

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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 10.40.2340.593wilson
Risk in group 20.4230.2550.611wilson
Risk difference, group 1 minus group 2-0.0231-0.2730.232newcombe hybrid score
Risk ratio, group 1 over group 20.9450.491.82log
Odds ratio, group 1 over group 20.9090.2982.78log
Number needed to treat, for one fewer participant with a serious adverse event on 70% Isopropyl Alcohol Novel Preoperative Skin Antiseptic than on 2% Chlorhexidine Gluconate/70% Isopropyl Alcohol Preoperative Skin Antiseptic
43.3from 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 170% Isopropyl Alcohol Novel Preoperative Skin Antiseptic70% v/v Isopropyl Alcohol novel preoperative skin antisepsis preparation~70% v/v Isopropyl Alcohol Surgical Solution: Patient preoperative skin preparation1025EG000
Group 22% Chlorhexidine Gluconate/70% Isopropyl Alcohol Preoperative Skin Antiseptic2% Chlorhexidine Gluconate/70% Isopropyl Alcohol preoperative skin antisepsis preparation~2%w/v Chlorhexidine Gluconate / 70% v/v Isopropyl Alcohol: Patient preoperative skin preparation1126EG001

Harm

What it counts
Total, serious adverse events
Time frame
AE's reported from time of enrollment through follow up (30 days post op), up to 51 days ( up to 21 days for screening).

Source ClinicalTrials.gov

Trial

Title
Perioperative Patient Skin Antiseptic Preparation Evaluation
NCT number
NCT04756804
Phases
PHASE3
Conditions
Surgical Site Infection
Interventions
70% v/v Isopropyl Alcohol Surgical Solution, 2%w/v Chlorhexidine Gluconate / 70% v/v Isopropyl Alcohol
Lead sponsor
Zurex Pharma, Inc.
Results first posted
2024-03-20

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/NCT04756804-sae