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Generated: February 22, 2019

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CLINICAL TRIALS PROFILE FOR CHLORAPREP WITH TINT

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Clinical Trials for Chloraprep With Tint

Trial ID Title Status Sponsor Phase Summary
NCT00290290 Efficacy Study of Antiseptic Preoperative Scrubs in Prevention of Postoperative Infections Completed Medical College of Wisconsin Phase 3 Most cases of infection of clean-contaminated wounds (wounds without gross spillage of organisms from the gastrointestinal tract) are thought to originate from the skin. Therefore, it is conceivable that application of an optimal antiseptic agent can reduce the rate of surgical wound infections. This trial is to compare the impact of disinfecting the skin with Chloraprep (2%chlorhexidine and 70% isopropyl alcohol) vs. Betadine on the rates of infection of clean-contaminated surgical wounds. The study will also assess the occurrence of adverse effects on the skin from either antiseptic agent and the cost-savings associated with the use of Chloraprep vs Betadine.
NCT00290290 Efficacy Study of Antiseptic Preoperative Scrubs in Prevention of Postoperative Infections Completed Michael Debakey Veterans Affairs Medical Center Phase 3 Most cases of infection of clean-contaminated wounds (wounds without gross spillage of organisms from the gastrointestinal tract) are thought to originate from the skin. Therefore, it is conceivable that application of an optimal antiseptic agent can reduce the rate of surgical wound infections. This trial is to compare the impact of disinfecting the skin with Chloraprep (2%chlorhexidine and 70% isopropyl alcohol) vs. Betadine on the rates of infection of clean-contaminated surgical wounds. The study will also assess the occurrence of adverse effects on the skin from either antiseptic agent and the cost-savings associated with the use of Chloraprep vs Betadine.
NCT00290290 Efficacy Study of Antiseptic Preoperative Scrubs in Prevention of Postoperative Infections Completed VA Office of Research and Development Phase 3 Most cases of infection of clean-contaminated wounds (wounds without gross spillage of organisms from the gastrointestinal tract) are thought to originate from the skin. Therefore, it is conceivable that application of an optimal antiseptic agent can reduce the rate of surgical wound infections. This trial is to compare the impact of disinfecting the skin with Chloraprep (2%chlorhexidine and 70% isopropyl alcohol) vs. Betadine on the rates of infection of clean-contaminated surgical wounds. The study will also assess the occurrence of adverse effects on the skin from either antiseptic agent and the cost-savings associated with the use of Chloraprep vs Betadine.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Chloraprep With Tint

Condition Name

Condition Name for Chloraprep With Tint
Intervention Trials
Surgical Site Infection 9
Surgical Skin Preparation 3
Infection 2
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Condition MeSH

Condition MeSH for Chloraprep With Tint
Intervention Trials
Surgical Wound Infection 10
Infection 5
Communicable Diseases 5
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Clinical Trial Locations for Chloraprep With Tint

Trials by Country

Trials by Country for Chloraprep With Tint
Location Trials
United States 27
Canada 2
Thailand 1
United Kingdom 1
Italy 1
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Trials by US State

Trials by US State for Chloraprep With Tint
Location Trials
Virginia 8
Montana 5
Pennsylvania 2
Maryland 2
Massachusetts 2
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Clinical Trial Progress for Chloraprep With Tint

Clinical Trial Phase

Clinical Trial Phase for Chloraprep With Tint
Clinical Trial Phase Trials
Phase 4 11
Phase 3 10
Phase 2 4
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Clinical Trial Status

Clinical Trial Status for Chloraprep With Tint
Clinical Trial Phase Trials
Completed 15
Recruiting 7
Not yet recruiting 4
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Clinical Trial Sponsors for Chloraprep With Tint

Sponsor Name

Sponsor Name for Chloraprep With Tint
Sponsor Trials
Zurex Pharma, Inc. 8
3M 4
CareFusion 3
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Sponsor Type

Sponsor Type for Chloraprep With Tint
Sponsor Trials
Other 21
Industry 18
U.S. Fed 2
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