Comparison between two techniques of anaesthesia

Phase 3

• Conditions: Health Condition 1: K009- Disorder of tooth development, unspecified

• Registration Number: CTRI/2022/02/040481
• Lead Sponsor: KLE VK institute of dental sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients who require bilateral orthodontic extractions of upper premolars

Patients with ASA status I and having normal bleeding & clotting time.

Exclusion Criteria

Patients unwilling to participate in the study.

Patients who have known history of allergy to the drugs or anesthetics used in the surgical protocol.

Patients on analgesics in the preceding 2 weeks.

Patients with infection or inflammation with upper premolar tooth

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To assess the post-operative painTimepoint: 15 mins and 1 day

Secondary Outcome Measures

Name	Time	Method
To assess onset and duration of the patchTimepoint: Every 30 sec for onset and 15-20 mins for duration