MedPath

Effectiveness of Lavage With Alcohol - Chlorhexidine for Chemical Matricectomy

Phase 4
Conditions
Ingrown Toenail
Interventions
Registration Number
NCT01844141
Lead Sponsor
Universidad Complutense de Madrid
Brief Summary

To compare the efficacy of the lavage with 70% alcohol plus 0.5% chlorhexidine versus 70% alcohol in the surgical treatment of ingrown toenails.

Detailed Description

The purpose of this study is to compare the efficacy of the lavage with 70% alcohol plus 0.5% chlorhexidine versus 70% alcohol during the phenolization procedure in the surgical treatment of ingrown toenails in patients undergoing for chemical matricectomy.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Older than 18 with onychocryptosis
Exclusion Criteria
  • infection, history of tinea pedis, onychomycosis, paronychia, nail trauma or subungual hematoma, nail deformities and disorders, peripheral vascular disease or diabetes, cardiac disease, history of rheumatic fever, recent antibiotic use or current antimicrobial therapy, history of steroid use and recent nail polish use

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
alcohol - clorhexidine70% alcohol - 0.5% clorhexidineIngrown toenail irrigated using 70% alcohol - 0.5% clorhexidine
70% alcohol70% alcoholIngrown toenail irrigated using 70% alcohol
Primary Outcome Measures
NameTimeMethod
Quantity of phenol recovered in each lavage with each solutionup to 2 weeks

The amounts of phenol in the samples were quantified by a Jasco modular high performance liquid chromatograph HPLC (Jasco International Co Ltd, Japan) equipped with a LG-2080-04 quaternary low-gradient unit, a PU-2080 pump, a DG-2080-54 degasser, an AS-2050-plus autosampler and a UV-2070 plus UV/Vis detector was used. A C18 column Luna (particle size 3 µm, 150 x 4.6 mm) (Phenomenex, Torrance, CA, USA) was selected for the chromatographic separation of the components, adjusting the column temperature to 30 °C (LC Ni-II/ADC oven).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Universidad Complutense de Madrid (Podología)

🇪🇸

Madrid, Spain

© Copyright 2025. All Rights Reserved by MedPath