Viewing Study NCT06293807



Ignite Creation Date: 2024-05-06 @ 8:13 PM
Last Modification Date: 2024-10-26 @ 3:22 PM
Study NCT ID: NCT06293807
Status: COMPLETED
Last Update Posted: 2024-03-08
First Post: 2024-02-27

Brief Title: Immediate Post-Operative Anesthesia With Either Lidocaine or Bupivacaine
Sponsor: The University of Texas Health Science Center at San Antonio
Organization: The University of Texas Health Science Center at San Antonio

Study Overview

Official Title: Immediate Post-Operative Anesthesia With Either Lidocaine or Bupivacaine A Short-term Clinical Response
Status: COMPLETED
Status Verified Date: 2024-03
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: Immediate post-suturing administration of either one of two dental anesthetic solutions or a placebo prior to dismissal
Detailed Description: This study seeks to evaluate the pain response following the administration of two anesthetic solutions just prior to patient dismissal from a surgical procedure 2 Xylocaine with 1100000 epi and 05 Bupivicaine with 1200000 epi in comparison with 09 Normal Saline as a placebo the study team will monitor pain response following these interventions at 4 8 12 24 and 48 hours

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
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