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To evaluate the effect of clove oil, betel leaf extract, lignocaine gels and ice for pain reduction during intraoral injections

Not Applicable
Conditions
Health Condition 1: K040- Pulpitis
Registration Number
CTRI/2020/12/029937
Lead Sponsor
Dr Kanchan M Tuppadmath
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

A) Children of age group of 6-10 years.

B) Children requiring administration of infiltration anesthesia irrespective of treatment.

C) Children with Franklâ??s behaviour rating 3 and 4.

D) Children with good general health (ASA I).

E) Children who are willing to participate and whose parents give informed consent.

Exclusion Criteria

A) Medically compromised children.

B) Patient with history of anxiety disorder.

C) Children or parents not willing to participate.

D) Patients with history of allergy to local anesthesia.

E) Patients on medication that can alter pain perception.

F) Children with active pathology at the administration site.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare and evaluate the pain perception following topical application of clove oil, betel leaf extract, lignocaine gels & ice prior to intraoral infilterations.Timepoint: 60 seconds after the application of comparator agents
Secondary Outcome Measures
NameTimeMethod
To evaluate for any adverse effects following topical application of comparator agentTimepoint: 60 seconds after the application of comparator agents
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