Ignite Creation Date:
2024-05-06 @ 7:44 AM
Last Modification Date:
2024-10-26 @ 11:52 AM
Study NCT ID:
NCT02595593
Status:
UNKNOWN
Last Update Posted:
2022-05-10
First Post:
2015-04-30
Brief Title:
Rib Fixation for Clinically Severe Rib Fractures From Trauma
Sponsor:
Darwin Ang
Organization:
SCRI Development Innovations LLC
Study Overview
Official Title:
A Multicenter Prospective Randomized Trial on the Intervention of Rib Fixation for Clinically Severe Rib Fractures From Trauma
Status:
UNKNOWN
Status Verified Date:
2022-05
Last Known Status:
RECRUITING
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:
SOFRIB
Brief Summary:
This is a multicenter randomized study investigating the differences in clinical outcomes of patients between two standard of care pathways for rib trauma patients who receive rib fixation versus patients who receive modern critical care and pain control after sustaining clinically significant rib fractures from trauma
Detailed Description:
This study will compare the outcomes of patients between two standard of care pathways for rib trauma those who have their ribs plated versus those who are managed by modern critical care and pain control A study nurse project coordinator will identify subjects based on inclusion and exclusion criteria then obtain consent for each of these patients prior to randomization Randomization will be decided by a web-based computer program accessible to the project coordinator Although this randomization occurs the study itself is purely observational as the intervention is currently standard of care None of the subjects or study group members will be blinded since it is not possible to disguise the intervention Patients will be evaluated and a survey will be administered at set post-intervention intervals to determine endpoints and quality of life when data analysis will also take place
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