Study of three types of treatment for leg ulcers of people with problems arising from leprosy

Not Applicable

• Conditions: leprosy; wounds and injuries; C01.252.410.040.552.386

• Registration Number: RBR-7rh8y2
• Lead Sponsor: Faculdade de Medicina de Botucatu UNESP

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-06-02
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Have treatment completed for leprosy confirmed in the medical record by ICD A30; have leg ulcer; both genres; Age between 18 and 90 years

Exclusion Criteria

Use of systemic antimicrobials; infected or critically colonized ulcers that present evidence of an infectious process.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Recruitment rate in the study for six months, calculated by the number of participants included in the study divided by the total number of eligible patients X 100.;Participants' adherence rate to the proposed treatment, calculated by the number of participants using the indicated product divided by the number of participants included X 100 and the rate of return to the assessments, calculated by the number of participants attending for reevaluation divided by the total number of participants included X 100.

Secondary Outcome Measures

Name	Time	Method
Efficacy of interventions in the three study groups: Hydrogel, zinc oxide 20% and zinc oxide 25%, obtained by comparing the median PUSH and Pain Scale scores obtained in the baseline evaluation with those obtained in the octave week post-treatment.