A Subjective Observational Study of Patients Using Medicated Footbath/Footwash Treatment in Podiatry Care

NCT ID: NCT03781024

Last Updated: 2018-12-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

5000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-12-01

Study Completion Date

2022-06-01

Brief Summary

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The purpose of this study is to evaluate the level of relief perceived by patients using medicated footbath/footwash with or without an oral medication for the treatment of podiatry issues.

Detailed Description

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Footwash/Footbath for treatment of; Toenail fungus Ingrown toenails Cellulitis Athletes' foot Pitted Keratolysis Diabetic ulcers Open infected sores Abscesses Joint infections Wound care

Conditions

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Toenail Fungal Infection Cellulitis Pitted Keratolysis Diabetic Foot Ulcer Abscess

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Footwash

footbath/footwash can help cleanse the wound, remove dead tissue, increase circulation and puts the wound in direct contact with medication to promote faster healing.

Intervention Type COMBINATION_PRODUCT

Other Intervention Names

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Footbath

Eligibility Criteria

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Inclusion Criteria

Participants must be diagnosed with an ICD10 code indicative of Toenail Fungus, Ingrown Toenail, Cellulitis, Athletes Foot, Pitted Keratolysis, Diabetic Ulcers, Open infected sores, Abscesses, and Joint infections

* Participants must be starting a new regimen of a medicated footwash/foothbath
* Participants must be expecting to receive therapy for at least 12 weeks
* Participants must be between 18 and 64 years of age
* Participants must be able to provide sound verbal informed consent

Exclusion Criteria

\-

Participants must not be a beneficiary of government funded healthcare program (i.e. Medicare, Medicaid, etc.)

• Participants must not have a diagnosis of cancer within the past 5 years
Eligible Sex

Accepts Healthy Volunteers

No

Sponsors

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Data Collection Analysis Business Management

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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DCABM

Land O' Lakes, Florida, United States

Site Status

Countries

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United States

Other Identifiers

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PAS1467

Identifier Type: -

Identifier Source: org_study_id