Behavior Management Device to reduce dental anxiety in children.
- Conditions
- Health Condition 1: - Health Condition 2: - Health Condition 3: F408- Other phobic anxiety disorders
- Registration Number
- CTRI/2022/07/044137
- Lead Sponsor
- Dr Ritesh Kalaskar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Healthy children with the non-contributory medical history
2.Children falling under Franklâ??s behavior rating scale 3 and 4
3.Children with class I, Class II and Class V cavities on primary maxillary or mandibular molars and canines
4.Each patient should have a minimum of 2-3 cavities on each side of the jaw.
5.Clinically the involved tooth should not have pulpal exposure
6.Radiographically, the caries should not extend to the pulp chamber
7.The tooth/teeth should be either asymptomatic or have a history of reversible pulpitis.
8.Children and their parents who are willing to participate in the study
1.Children with special health care needs.
2.Children with carious lesion approaching or extending into the pulp (clinically and radiographically)
3.Children with a history of abscess or sinus tract formation, swelling, non-restorable teeth or mobile teeth.
4.Patients and their parents who are unwilling to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate and compare heart rate, oxygen saturation and blood pressure of children during dental procedure using biofeedback dental anxiety regulator <br/ ><br>To evaluate and compare pulse heart rate, oxygen saturation and blood pressure of children during dental procedure using virtual reality eyeglasses. <br/ ><br>To evaluate and compare dental anxiety of children of both the groups during dental procedure <br/ ><br>To evaluate and compare dental anxiety of the children of both the groups by another investigator.Timepoint: 1.before the procedure <br/ ><br>2.during the procedure at an interval of 3 mins <br/ ><br>3.after the procedure
- Secondary Outcome Measures
Name Time Method not applicableTimepoint: not applicable