Viewing Study NCT02543619



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Last Modification Date: 2024-10-26 @ 11:49 AM
Study NCT ID: NCT02543619
Status: COMPLETED
Last Update Posted: 2015-09-07
First Post: 2015-09-04

Brief Title: Efficacy of Two Injection Techniques on Success Rate of Inferior Alveolar Nerve Anesthesia
Sponsor: Azad University of Medical Sciences
Organization: Azad University of Medical Sciences

Study Overview

Official Title: Comparative Efficacy of Gow-Gates and Inferior Alveolar Nerve Block Injection Techniques on Success Rate of Anesthesia in Patients With Symptomatic Irreversible Pulpitis
Status: COMPLETED
Status Verified Date: 2015-09
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: Forty healthy patients with including criteria who failed to infra alveolar nerve block injection without lip numbness have been randomly divided into two groups on a random basis and have received Gow-Gates or another inferior alveolar nerve block injection Endodontic access cavity preparation has been initiated after complete anesthesia If patients felt any pain during the steps of caries or dentin removal Endodontic access cavity preparation or canal working length determination treatment has been stopped and their pain has been measured by Heft Parker 170 mm Visual Analog Scale Zero as no pain and 170 as maximum pain The data has been analyzed by Mann-U-Whitney and CHI- SQUARE tests
Detailed Description: The aim of this study was to assess the efficacy of Gow-Gates and inferior alveolar nerve block on success rate of anesthesia in patients with irreversible pulpitis In this prospective randomized double-blind study forty healthy patients with symptomatic irreversible pulpitis and including criteria who failed to infra alveolar nerve block injection without lip numbness have been randomly divided into two groups on a random basis and have received Gow-Gates or another inferior alveolar nerve block injection Their pain has been evaluated by electric pulp tester every 5 minutes for two times Endodontic access cavity preparation has been initiated after complete anesthesia If patients felt any pain during the steps of caries or dentin removal Endodontic access cavity preparation or canal working length determination treatment has been stopped and their pain has been measured by Heft Parker 170 mm Visual Analog Scale Zero as no pain and 170 as maximum pain The patients have been instructed to rate any pain during each of the mentioned steps The data have been analyzed by Mann-U-Whitney and CHI- SQUARE tests

Study Oversight

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