CTRI/2022/10/046373Not yet recruiting未知
To evaluate the efficacy of a Neuromodulation device in management of pain after interproximal reduction: An in vivo study.
Anu Nain0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
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.
Investigators
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