Viewing Study NCT05239078



Ignite Creation Date: 2024-05-06 @ 5:14 PM
Last Modification Date: 2024-10-26 @ 2:24 PM
Study NCT ID: NCT05239078
Status: COMPLETED
Last Update Posted: 2022-02-14
First Post: 2022-01-24

Brief Title: Comparative Evaluation of Pulpal Anaesthetic Efficacy of Different Anaesthetic Solutions for Inferior Alveolar Nerve Block in Patients With Symptomatic Irreversible Pulpitis
Sponsor: Dr Vivek Aggarwal
Organization: Jamia Millia Islamia

Study Overview

Official Title: Comparative Evaluation of Pulpal Anaesthetic Efficacy of Different Anaesthetic Solutions for Inferior Alveolar Nerve Block in Patients With Symptomatic Irreversible Pulpitis a Randomized Double-blind Study
Status: COMPLETED
Status Verified Date: 2022-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Pulpal and periapical inflammation and infection can cause tissue pH in the affected region to be lowered which results in less penetration of anesthetic solution in the nerve membrane and hence delays the onset of anesthesia So the purpose of this study was to compare the pulpal anesthetic efficacy of lidocaine articaine mepivacaine for inferior alveolar nerve block IANB in patients with irreversible pulpitis IP One hundred and twenty adult patients with IP concerning mandibular molars randomly received IANB with either of the three solutions 2 lidocaine with epinephrine 4 articaine with epinephrine 3 plain mepivacaine Pain during the endodontic treatment was assessed using a visual analog scale Heft-Parker VAS Endodontic treatment was initiated Success was defined as no or mild pain pain score54mm on Hp VAS during access preparation and root canal instrumentation The anesthetic success rates were analyzed with the chi-square test
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None