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

Weill Medical College of Cornell University

Overview

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

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Conditions

Nail Diseases

Interventions

Hydrophilic polymer and potassium ferrate powderDEVICE

Application with pressure until hemostasis is achieved

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Weill Cornell Medicine

New York, New York, United States

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

Time frame: Baseline

Secondary Outcomes

Number of participants with at least one adverse event

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

Time frame: End of study (28 days)

Data from ClinicalTrials.gov

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