Comparaison of Pain and Anxiety of patient using different anesthesia techniques

Comparative Evaluation of Pain Perception and Anxiety of patient using different techniques of Inferior alveolar nerve block in mandibular teeth with symptomatic irreversible pulpitis using a newly introduced device & its components and the conventional syringe technique A randomized clinical study - NIL

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065203

Enrollment

Registered

2024-04-04

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: VIBRATING, COOLING AND COMPLETE BUZZY DEVICE: THERE WILL BE 3 GROUPS IN WHICH 1ST GROUP WILL INVOLVE USING ONLY VIBRATING PART OF BUZZY DEVICE, 2ND GROUP WILL INVOLVE USING ONLY COOLING

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

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

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Ajay Singh Rao

KM SHAH DENTALCOLLEGE

drajayinendo@gmail.com8385017307

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026