Ignite Creation Date:
2024-10-25 @ 8:02 PM
Last Modification Date:
2024-10-26 @ 3:39 PM
Study NCT ID:
NCT06588907
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-08
Brief Title:
Pain Palliation in Forearm Fractures in the Emergency Department
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Evaluation of the Efficacy of Procedural Sedoanalgesia and Infraclavicular Nerve Blockade on Analgesia in Forearm Fractures in the Emergency Department
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim is to evaluate the success of reduction procedures and pain palliation in patients with forearm fractures undergoing reduction under procedural sedation-analgesia PSA and ultrasound US-guided infraclavicular nerve block ICB in the emergency department
Detailed Description:
Forearm fractures are among the most frequent reasons for adults to visit the emergency department These fractures cause significant pain both due to the fracture itself and during the reduction process Pain management in emergency departments ED is crucial Therefore multimodal approaches are available to reduce or eliminate pain during the reduction process The aim of this study is to evaluate the success and pain palliation of the reduction process with procedural sedation-analgesia PSA and with reduction under ultrasound US-guided infraclavicular nerve block ICB in patients with forearm fractures The secondary aim is to compare patient comfort physician comfort side effects length of stay in the emergency department and the need for painkillers after discharge between these two procedures and to identify the most suitable method This study aims to contribute to practical applications in order to provide optimal pain control in patients with forearm fractures in emergency departments
Patients pain levels at arrival pre-reduction procedure and post-reduction procedure will be recorded using the Numeric Rating Scale NRS ranging from 0 no pain to 10 worst imaginable painThe success of the reduction procedure whether further reduction attempts were necessary and findings from post-reduction control X-rays radial height radial tilt and volar tilt will be noted and evaluated by orthopedic physicians
Patients pain levels at arrival pre-reduction procedure and post-reduction procedure will be recorded using the Numeric Rating Scale NRS ranging from 0 no pain to 10 worst imaginable painThe success of the reduction procedure whether further reduction attempts were necessary and findings from post-reduction control X-rays radial height radial tilt and volar tilt will be noted and evaluated by orthopedic physicians
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