MedPath

Scar and Joint Pain treatment using BEST device

Phase 1
Registration Number
CTRI/2017/05/008566
Lead Sponsor
Avazzia Inc
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

i) Subjects with any type of scar OR

ii) Subjects with scar associated with pain

Exclusion Criteria

i) Subjects below 18 years of age

ii)Subjects who are pregnant, with implanted pacemaker or any such devices

ii) Subjects with any neurological conditions

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
i) Evaluating the functionality of the device <br/ ><br>ii) Relief of knee joint pain <br/ ><br>iii) Scar reduction <br/ ><br>iv) Publications to highlight the pros and cons of the deviceTimepoint: 3 months duration
Secondary Outcome Measures
NameTimeMethod
i) Evaluating the functionality of the device <br/ ><br>ii) Relief of knee joint pain <br/ ><br>iii) Scar reduction <br/ ><br>iv) Publications to highlight the pros and cons of the deviceTimepoint: 3 months
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