Scar and Joint Pain treatment using BEST device

Study of BEST device for scar treatment and joint pain relief

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2017/05/008566

Enrollment

Registered

2017-05-16

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Interventional Group: Patients with scar or joint pain before and after BEST therapy Control Intervention1: Control Group: Patients with scar or joint pain without BEST therapy

Eligibility

Inclusion criteria

Inclusion criteria: i) Subjects with any type of scar OR ii) Subjects with scar associated with pain

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
i) Evaluating the functionality of the device ii) Relief of knee joint pain iii) Scar reduction iv) Publications to highlight the pros and cons of the deviceTimepoint: 3 months duration	—

Secondary

Measure	Time frame
i) Evaluating the functionality of the device ii) Relief of knee joint pain iii) Scar reduction iv) Publications to highlight the pros and cons of the deviceTimepoint: 3 months	—

Countries

India

Contacts

Public ContactDr Dinesh Bhatia

North Eastern Hill University

bhatiadinesh@rediffmail.com03642723853

Outcome results