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

Weill Cornell Medicine (WCM)

Status and phase: Withdrawn; Phase 4

Conditions: Nail Diseases

Treatments: Device: Hydrophilic polymer and potassium ferrate powder

Study type: Interventional

Funder types: Other

Identifiers

NCT04384679

20-02021562

Details and patient eligibility

About

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

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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0 participants in 2 patient groups

Hydrophilic polymer and potassium ferrate powder

Experimental group

Description:

Hydrophilic polymer with potassium ferrate powder is applied to the surgical wound with pressure until hemostasis is achieved

Treatment:

Device: Hydrophilic polymer and potassium ferrate powder

Direct pressure with sterile gauze

No Intervention group

Description:

Direct pressure with sterile gauze is applied to the surgical wound until hemostasis is achieved