Benefit of Topical Hemostatic Powder Containing Hydrophilic Polymer With Potassium Ferrate for Hemostasis Following Nail Surgery
NCT ID: NCT04384679
Last Updated: 2022-08-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
PHASE4
INTERVENTIONAL
2022-06-30
2023-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Hydrophilic polymer and potassium ferrate powder
Hydrophilic polymer with potassium ferrate powder is applied to the surgical wound with pressure until hemostasis is achieved
Hydrophilic polymer and potassium ferrate powder
Application with pressure until hemostasis is achieved
Direct pressure with sterile gauze
Direct pressure with sterile gauze is applied to the surgical wound until hemostasis is achieved
No interventions assigned to this group
Interventions
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Hydrophilic polymer and potassium ferrate powder
Application with pressure until hemostasis is achieved
Eligibility Criteria
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Inclusion Criteria
* Patients scheduled for any type of nail surgical procedure
* Willingness to participate in the study
* Ability to understand all instructions in the English language
Exclusion Criteria
* Likely inability to comply with the study protocol or cooperate fully with the research team
18 Years
ALL
No
Sponsors
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Weill Medical College of Cornell University
OTHER
Responsible Party
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Principal Investigators
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Shari R Lipner, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University
Locations
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Weill Cornell Medicine
New York, New York, United States
Countries
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Other Identifiers
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20-02021562
Identifier Type: -
Identifier Source: org_study_id
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