Clinical study to evaluate Pain perception after Interproximal reduction Using Neuromodulation Device .
Not Applicable
- Conditions
- Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified
- Registration Number
- CTRI/2022/10/046373
- Lead Sponsor
- Anu Nain
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients with mild to moderate crowding with non extraction.
2.Patient in finishing stage orthodontic treatment on rectangular stainless steel wire.
3.No E- chain will applied after IPR is performed.
4.Same appliance and prescription is used in all patients.
5.Same method of ligation is applied in all patients.
6.Patients with good dental health.
7.Patients in any phase of orthodontic treatment.
Exclusion Criteria
1.Patients susceptible to tooth decay.
2.History of seizures, cardiac arrythmia or pacemaker treatment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method