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Comparison · NCT02402907-0ef8e990

CHG Cloth vs Placebo Cloth: Number of Adherent Participants With Incisional SSI

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. CHG Cloth vs Placebo Cloth: Number of Adherent Participants With Incisional SSI. Trial comparisons, record NCT02402907-0ef8e990. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02402907-0ef8e990

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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 10.01910.01040.0348wilson
Risk in group 20.0330.02070.0522wilson
Risk difference, group 1 minus group 2-0.0139-0.0350.00601newcombe hybrid score
Risk ratio, group 1 over group 20.5780.2671.25log
Odds ratio, group 1 over group 20.570.2581.26log
Number needed to treat, for one fewer participant with the outcome on CHG Cloth than on Placebo Cloth71.8from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CHG Cloth2% chlorhexidine gluconate (CHG) cloth: administration of a 2% CHG cloth at home on the night before and approximately 3 hours prior to cesarean delivery on the morning of the surgery.10524OG000
Group 2Placebo Cloth
Placebo cloth: administration of a fragrance free cleansing cloth with the placebo (commercial cleansing cloth) at home on the night before and approximately 3 hours prior to cesarean delivery on the morning of the surgery.
17515OG001

Outcome

Type
PRIMARY
Title
Number of Adherent Participants With Incisional SSI
Description
Among those with full adherence to the protocol and who were available for assessment at 6 weeks. Adherence to the protocol was assessed in the following 2 ways: evaluation of returned packages on the day of surgery and report ascertained by phone interview at 2 weeks.
Time frame
at 6 weeks
Population
participants with full adherence to protocol and available for assessment at 6 weeks

Source ClinicalTrials.gov

Trial

Title
STRIPES Study: Study To Reduce Infection Post cEsarean Section
NCT number
NCT02402907
Phases
NA
Conditions
Chlorhexidine Gluconate Cloths, Infection; Cesarean Section, Infectious Morbidity, Surgical Site Infections, Endometritis
Interventions
2% chlorhexidine gluconate (CHG) cloth, Placebo cloth
Lead sponsor
Icahn School of Medicine at Mount Sinai
Results first posted
2020-11-09

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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