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Clinical Trial Summary

The objective of the study is to demonstrate the antimicrobial efficacy of the Zurex Preoperative Prep (ZuraPrep - clear) on skin flora of the abdomen and inguinal regions of human subjects.


Clinical Trial Description

The primary objective of this study is to measure the antimicrobial effectiveness of a single investigational test article, ZuraPrep™ as specified by the Healthcare Antiseptics, Topical Antimicrobial Drug Products Final Rule of December 20, 2017. The treatments will be ZuraPrep™ as the investigational test article, ChloraPrep® as an active control, and ZuraPrep™ Vehicle as a negative control. For efficacy at 30 seconds post-prep, the test article should be superior to the negative control using a margin of 1.2 log10 CFU/cm2 and non-inferior to the active control using a margin of 0.5 log10 CFU/cm2. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03782103
Study type Interventional
Source Zurex Pharma, Inc.
Contact
Status Completed
Phase Phase 3
Start date January 25, 2019
Completion date September 26, 2019

See also
  Status Clinical Trial Phase
Completed NCT03681990 - In Vivo Preoperative Skin Preparation Efficacy Study Within a Defined Product Coverage Area Phase 2
Completed NCT04756154 - Efficacy Study of Patient Preoperative Preps In-vivo Phase 3
Completed NCT02831998 - In-vivo Efficacy of Patient Preoperative Prep Phase 3
Completed NCT03331263 - Single Dose CHG Pharmacokinetic Study Phase 1
Completed NCT02831816 - Clinical Evaluation of Patient Preoperative Prep Phase 3