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Clinical study to evaluate Pain perception after Interproximal reduction Using Neuromodulation Device .

To evaluate the efficacy of a Neuromodulation device in management of pain after interproximal reduction: An in vivo study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046373
Enrollment
30
Registered
2022-10-11
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified

Interventions

Intervention1: Neuromodulation Device: pain reduction after IPR by using Neuromodulation Device at 0hours ,24hours and 48 hours. Control Intervention1: Neuromodulation Device: Reduction in pain percep

Sponsors

Anu Nain
Lead Sponsor

Eligibility

Inclusion 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

Exclusion criteria: 1. Patients susceptible to tooth decay. 2. History of seizures, cardiac arrythmia or pacemaker treatment.

Design outcomes

Primary

MeasureTime frame
Reduction in pain perception .Timepoint: 0,24,48hours.—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactAnu Nain

Sudha Rustagi College of Dental Sciences & Research

sridharnoopur@gmail.com9818212912

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026