Comparaison of Pain and Anxiety of patient using different anesthesia techniques

Phase 1

Completed

• Conditions: Health Condition 1: K040- Pulpitis

• Registration Number: CTRI/2024/04/065203
• Lead Sponsor: Dikshit Mahendra Solanki

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2024-04-22
• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

1.Patients with Pre-operative moderate to severe pain i.e. VAS score of 4 and above in teeth with symptomatic irreversible pulpitis will be included in the study.

2.Patients not having prior experience of administration of Local anesthesia will be included in the study.

3.Patients showing Delayed response to cold and electric pulp testing (EPT) will be included in the study.

4.Patients with symptomatic irreversible pulpitis with/without symptomatic apical periodontitis (only vital teeth) will be included in the study.

5. Patients without any inflammation or trauma on the external surface of concerned cheek will be included in the study.

6.A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.

Exclusion Criteria

1.Asymptomatic Non-Vital Teeth with/without periapical radiolucency be it abscess or granuloma etc will be excluded.

2.Patients showing active sites of pathosis in the injection area.

3.Medically compromised patients will be excluded.

4.Teeth with completely obliterated canals will be excluded

5.Teeth with open apex, root resorption or complex root canal anatomy will be excluded.

6.Teeth with vertical root fractures, cracks, etc will be excluded.

7.Patient with deep periodontal disease or endo-perio lesion with periodontal phase dominant will be excluded.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
WHETHER THE PAIN PERCEPTION AND ANXIETY LEVELS ARE REDUCED USING THIS NEW TECHNIQUETimepoint: after 10 mins, 30 minutes and 60 minutes

Secondary Outcome Measures

Name	Time	Method
ILTimepoint: NI