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Topical Collagen-Silver Versus Standard Care Following Removal of Ingrown Nails

Sponsored by Rosalind Franklin University of Medicine and Science

About this trial

Last updated 17 years ago

Study ID

ORT 014

Status

Unknown status

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
18+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 17 years ago

What is this trial about?

This study's purpose is to prospectively determine whether topical therapy with an oxidized regenerated cellulose collagen-silver compound is more effective than the current standard of topical antibiotic therapy for care following the removal of an ingrown toenail. Eighty adult patients with ingrown toenails will be recruited. Each patient will randomly be assigned to apply either topical silver sulfadiazine cream (standard antibiotic) or the novel collagen-silver compound to their nail bed daily, following removal of the ingrown portion of nail. Patients will return for follow up visits weekly, until healing has occurred or twelve weeks have passed. Healing will be defined as resolution of drainage and inflammatory changes surrounding the nail border.

What are the participation requirements?

Yes

Inclusion Criteria

- Ingrown toenails will be defined as any incurvated nail border that digs into the skin of the nail fold and causes pain and discomfort

No

Exclusion Criteria

- Patients with immunocompromised states

- chronic steroid use
- diabetes mellitus
- collagen vascular disease
- HIV infection

- Cellulitis proximal to the hallux interphalangeal joint or peripheral vascular disease will be excluded

- We will define peripheral vascular disease as the absence of one or more pedal pulses or the presence of dystrophic changes to the integument