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Benefit of Topical Hemostatic Powder Containing Hydrophilic Polymer With Potassium Ferrate for Hemostasis Following Nail Surgery

Phase 4
Withdrawn
Conditions
Nail Diseases
Registration Number
NCT04384679
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

The purpose of this study is to assess the efficacy and safety of topical hemostatic powder containing hydrophilic polymer with potassium ferrate for bleeding control after nail surgical procedures

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • At least 18 years old
  • 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
  • Failure to have nail surgery performed
  • Likely inability to comply with the study protocol or cooperate fully with the research team

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Time (in seconds) to bleeding cessation with hydrophilic polymer and potassium ferrate; time (in seconds) to bleeding cessation with direct pressure with sterile gauzeBaseline

Time (in seconds) will be measured from application of intervention/nonintervention until bleeding cessation

Secondary Outcome Measures
NameTimeMethod
Number of participants with at least one adverse eventEnd of study (28 days)

Adverse events will only include those that are determined to be related to the study device

Trial Locations

Locations (1)

Weill Cornell Medicine

🇺🇸

New York, New York, United States

Weill Cornell Medicine
🇺🇸New York, New York, United States

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