Ignite Creation Date:
2024-05-06 @ 7:27 PM
Last Modification Date:
2024-10-26 @ 3:07 PM
Study NCT ID:
NCT06017674
Status:
COMPLETED
Last Update Posted:
2023-08-30
First Post:
2023-08-24
Brief Title:
Intra-articular Pulsed Radiofrequency in Chronic Knee Pain
Sponsor:
Başakşehir Çam Sakura City Hospital
Organization:
Başakşehir Çam Sakura City Hospital
Study Overview
Official Title:
The Effectiveness of Intra-articular Pulsed Radiofrequency in Patients With Painful Knee Osteoarthritis
Status:
COMPLETED
Status Verified Date:
2023-08
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 aim of this study is to investigate the additional effect of Intra-articular Pulsed Radiofrequency IAPRF on pain and functional activities in addition to intra-articular steroids in patients with grade II and III knee osteoarthritis
Detailed Description:
This randomized controlled trial included patients over 18 years of age with knee pain persisting for more than 3 months and stage II-III knee OA according to the Kellgren-Lawrence scale The participants were randomized into two groups the IAPRF steroid injection Group 1 and only steroid injection Group 2 groups The injections were administered under fluoroscopic guidance in both groups and the needle was advanced to the midline of the tibiofemoral joint in the anteroposterior and lateral views Group 1 received 8 mg of intra-articular dexamethasone after IAPRF application for 360 s at 45 V voltage with the temperature not exceeding 42C Group 2 received 8 mg of intra-articular dexamethasone only Pain intensity and participation in daily activities were evaluated using the numerical rating scale NRS and Western Ontario and McMaster Universities arthritis index WOMAC respectively before the procedure and 1 4 and 12 weeks after the procedure
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?:
False
Is an FDA AA801 Violation?:
None