Ignite Creation Date:
2024-05-06 @ 3:18 PM
Last Modification Date:
2024-10-26 @ 1:46 PM
Study NCT ID:
NCT04582123
Status:
COMPLETED
Last Update Posted:
2020-10-09
First Post:
2020-10-05
Brief Title:
Comparison of Cross Pin Configurations in Supracondylar Humerus Fracture Treatment 2 Pins Versus 3 Pins
Sponsor:
Bakirkoy Dr Sadi Konuk Research and Training Hospital
Organization:
Bakirkoy Dr Sadi Konuk Research and Training Hospital
Study Overview
Official Title:
The Comparison of Cross Pin Configurations in the Treatment of Gartland Type III Supracondylar Humerus Fractures 2 Pins Versus 3 Pins
Status:
COMPLETED
Status Verified Date:
2020-10
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:
The objective of this prospective randomized controlled trial is to evaluate and compare the outcome of the 2wire vs 3 wire crossed pin configurations in the management of supracondylar humeral fractures in children
Detailed Description:
Fortyfive children with supracondylar humeral fractures were randomly divided into two groups One group was treated with 2 crossed pins and the other group with 3 crossed pins The mean age was 604249 1-12 The follow-up period was 5 years with no patients lost to follow up
Intervention Twentytwo patients were managed by 2 crossed and 23 by 3 crossed pin method All surgeries were performed by the same surgeon
Main Outcome Measurements Postoperative stability ulnar nerve injury range of motions and pin tract infections were evaluated
Intervention Twentytwo patients were managed by 2 crossed and 23 by 3 crossed pin method All surgeries were performed by the same surgeon
Main Outcome Measurements Postoperative stability ulnar nerve injury range of motions and pin tract infections were evaluated
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