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Anesthesia of lower teeth with different methods

Completed
Conditions
Patients should be actively experiencing pain in a mandibular premolar
Patients should be actively experiencing pain in a mandibular premolar.
Registration Number
CTRI/2017/03/008204
Lead Sponsor
Self funded
Brief Summary

The inferior alveolar nerve block (IANB) is the most commonly used technique for achieving pulpal anesthesia for posterior mandibular endodontic procedures. In mandibular premolars, buccal infiltration provides adequate anesthesia. The purpose of this prospective randomized study is to compare IANB and buccal infiltration on anesthetic success rates. Adult volunteer subjects will be selected from dental OPD and included in this prospective, randomized study. The success is defined as the ability to undertake pulp access and canal instrumentation with no or mild pain (Heft-Parker VAS score<55mm). The subjects should be actively experiencing pain and in good health, and none will be taking any medication that would alter pain perception, as determined by oral questioning and written questionnaire. An informed written consent will be obtained from each subject. The patients will be randomly allocated to the treatment groups. Patients will receive standard inferior alveolar nerve block or buccal infiltrations. A conventional access opening will be initiated after isolation with a rubber dam. Patients will be instructed to raise their hand if any pain was felt during the procedure. In case of pain during the treatment, the procedure will be stopped, and patients asked to rate the pain on HP VAS. Success will be defined as no pain or weak/mild pain during endodontic access preparation and instrumentation .

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
100
Inclusion Criteria

The subjects should be actively experiencing pain and in good health, and none will be taking any medication that would alter pain perception.

Exclusion Criteria

Patients with underlying systemic diseases.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ability to undertake pulp access and canal instrumentation with no or mild painThe primary outcome shall be assessed after the administration of local anesthetic solution and during the procedure. If the patient experiences pain during any point of the procedure the anesthesia will be considered as failure.
Secondary Outcome Measures
NameTimeMethod
ability to undertake pulp access and canal instrumentation with no or mild painIt will assessed at the end of the endodontic treatment.

Trial Locations

Locations (1)

Faculty of Dentistry, Jamia Millia Islamia

🇮🇳

South, DELHI, India

Faculty of Dentistry, Jamia Millia Islamia
🇮🇳South, DELHI, India
Dr Vivek Aggarwal
Principal investigator
9818188358
drvivekaggarwal@gmail.com

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