A clinical study to evaluate the pain perception during initial phase of orthodontic treatment using neuromodulation device.
Not Applicable
- Conditions
- Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified
- Registration Number
- CTRI/2022/10/046437
- Lead Sponsor
- Sachin Philip
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients ranging from the age of 11 to 17 years are selected for the study.
2. Patients with mild to moderate crowding with non-extraction orthodontic treatment
planning.
3. Patients with good dental health.
4. Patients in levelling and alignment phase of orthodontic treatment.
Exclusion Criteria
1. Pregnant patients.
2. Patients with the history of seizures, cardiac arrythmia or pacemaker treatment.
3. Patients who were taking any over the counter or prescription pain medication during
the testing period
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in pain perception.Timepoint: 0,24,48 hours
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI