Efficacy Study to Evaluate Antimicrobial Effectiveness of ZuraPrep™ (ZX-ZP-0055)
NCT02296645 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 36
Last updated 2016-07-14
Summary
This is a randomized, paired-comparisons design where each subject receives two of the planned treatments.
Conditions
- Surgical Site Infection
Interventions
- DRUG
-
ZuraPrep
Apply topically.
- DRUG
-
ChloraPrep
Apply topically.
Sponsors & Collaborators
-
Zurex Pharma, Inc.
lead INDUSTRY
Principal Investigators
-
M. Hamid Bashir, MD · MicroBioTest, Division of Microbac Laboratories, Inc.
Study Design
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2014-11-30
- Primary Completion
- 2015-01-31
- Completion
- 2015-01-31
Countries
- United States
Study Locations
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