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Clinical Trials/NCT04384679
NCT04384679
Withdrawn
Phase 4

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

ConditionsNail Diseases

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Nail Diseases
Sponsor
Weill Medical College of Cornell University
Locations
1
Primary Endpoint
Time (in seconds) to bleeding cessation with hydrophilic polymer and potassium ferrate; time (in seconds) to bleeding cessation with direct pressure with sterile gauze
Status
Withdrawn
Last Updated
3 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
June 2022
End Date
December 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Time (in seconds) to bleeding cessation with hydrophilic polymer and potassium ferrate; time (in seconds) to bleeding cessation with direct pressure with sterile gauze

Time Frame: Baseline

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

Secondary Outcomes

  • Number of participants with at least one adverse event(End of study (28 days))

Study Sites (1)

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