Ignite Creation Date:
2024-05-06 @ 8:22 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06352255
Status:
COMPLETED
Last Update Posted:
2024-04-08
First Post:
2023-10-26
Brief Title:
Pain and Anxiety During Local Block
Sponsor:
University of Seville
Organization:
University of Seville
Study Overview
Official Title:
Analysis of Pain and Anxiety With Carpule vs Syringe in Digital Anesthesia of the Hallux
Status:
COMPLETED
Status Verified Date:
2024-07
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:
INTRODUCTION Currently there is no scientific evidence about pain in the anesthetic blockage of the first finger according to the application method However clinical evidence has valued the use of carpule due to the low pain it generates in the patient to the application of anesthetic Most studies on anesthesia and pain especially with the use of carpule and distracting methods belong to the field of dentistry
OBJECTIVES It is intended to determine the pain after an anesthetic block in H of Frost in the first finger with different application methods such as syringe and carpule As secondary objectives it is intended to establish the difference in pain according to the sex and age of the patients
METHODOLOGY Experimental transverse and random clinical trial type analytical study in which a sample of 200 individuals will be selected 100 per group which would require digital anesthesia of the first finger and that would fulfill the inclusion criteria
Result after the completion of the study CONCLUSIONS After the completion of the study
OBJECTIVES It is intended to determine the pain after an anesthetic block in H of Frost in the first finger with different application methods such as syringe and carpule As secondary objectives it is intended to establish the difference in pain according to the sex and age of the patients
METHODOLOGY Experimental transverse and random clinical trial type analytical study in which a sample of 200 individuals will be selected 100 per group which would require digital anesthesia of the first finger and that would fulfill the inclusion criteria
Result after the completion of the study CONCLUSIONS After the completion of the study
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