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Effect of audio visual distraction on pain during pulp extirpatio

Not Applicable
Conditions
Health Condition 1: K040- Pulpitis
Registration Number
CTRI/2021/06/034189
Lead Sponsor
sahithi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
180
Inclusion Criteria

1) Subjects with acute irreversible pulpitis in mandibular molars

2) The subjects should be requiring endodontic intervention in at least one tooth and has a healthy tooth in a different quadrant.

3) The subjects should be actively experiencing pain and in good health.

Exclusion Criteria

1) Patients already taking anxiolytic or psychotropic medications,

2) Patients using analgesic or anti-inflammatory drugs

3) Patients with any visual or auditory deficits,

4) Patients who cannot communicate efficiently due to illiteracy or language barriers.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
If an audiovisual device worn during pulp extirpation can reduce the pain threshold.Timepoint: the outcome is assessed at the base line. i.e. immedietly after the intervention
Secondary Outcome Measures
NameTimeMethod
if audiovisual deice worn reduces pulp sensibilityTimepoint: the outcome is assessed at the base line. i.e. immedietly after the intervention
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