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Last Updated: November 22, 2024

CLINICAL TRIALS PROFILE FOR MAFENIDE ACETATE


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All Clinical Trials for MAFENIDE ACETATE

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00586729 ↗ Vashe Wound Therapy Study Completed PuriCore, Inc. N/A 2009-07-01 This study will evaluate the efficacy, safety, and tolerability of topical Vashe™ Wound Therapy applied to gauze dressing every 6 hours or as necessary to keep dressing moist versus 5% Mafenide Acetate applied to gauze dressing every 6 hours or as necessary to keep dressing moist for a total treatment duration of 5 days.
NCT00586729 ↗ Vashe Wound Therapy Study Completed Maricopa Integrated Health System N/A 2009-07-01 This study will evaluate the efficacy, safety, and tolerability of topical Vashe™ Wound Therapy applied to gauze dressing every 6 hours or as necessary to keep dressing moist versus 5% Mafenide Acetate applied to gauze dressing every 6 hours or as necessary to keep dressing moist for a total treatment duration of 5 days.
NCT00586729 ↗ Vashe Wound Therapy Study Completed Valleywise Health N/A 2009-07-01 This study will evaluate the efficacy, safety, and tolerability of topical Vashe™ Wound Therapy applied to gauze dressing every 6 hours or as necessary to keep dressing moist versus 5% Mafenide Acetate applied to gauze dressing every 6 hours or as necessary to keep dressing moist for a total treatment duration of 5 days.
NCT00634166 ↗ Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group Terminated Mylan Pharmaceuticals Phase 4 2007-09-01 The primary objective is to compare the effectiveness of treatment with Sulfamylon® solution as the initial topical moist dressing over meshed autografts following the initial graft procedure on preventing graft loss in a prospective cohort of subjects versus a historical control group in a non-inferiority trial.
NCT00634166 ↗ Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group Terminated Mylan Bertek Pharmaceuticals Phase 4 2007-09-01 The primary objective is to compare the effectiveness of treatment with Sulfamylon® solution as the initial topical moist dressing over meshed autografts following the initial graft procedure on preventing graft loss in a prospective cohort of subjects versus a historical control group in a non-inferiority trial.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for MAFENIDE ACETATE

Condition Name

Condition Name for MAFENIDE ACETATE
Intervention Trials
Burns 2
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Condition MeSH

Condition MeSH for MAFENIDE ACETATE
Intervention Trials
Burns 2
Wounds and Injuries 1
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Clinical Trial Locations for MAFENIDE ACETATE

Trials by Country

Trials by Country for MAFENIDE ACETATE
Location Trials
United States 9
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Trials by US State

Trials by US State for MAFENIDE ACETATE
Location Trials
Missouri 1
Maryland 1
Kansas 1
Illinois 1
Florida 1
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Clinical Trial Progress for MAFENIDE ACETATE

Clinical Trial Phase

Clinical Trial Phase for MAFENIDE ACETATE
Clinical Trial Phase Trials
Phase 4 1
N/A 1
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Clinical Trial Status

Clinical Trial Status for MAFENIDE ACETATE
Clinical Trial Phase Trials
Completed 1
Terminated 1
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Clinical Trial Sponsors for MAFENIDE ACETATE

Sponsor Name

Sponsor Name for MAFENIDE ACETATE
Sponsor Trials
Maricopa Integrated Health System 1
Valleywise Health 1
Mylan Pharmaceuticals 1
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Sponsor Type

Sponsor Type for MAFENIDE ACETATE
Sponsor Trials
Industry 3
Other 2
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