Viewing Study NCT06520371



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06520371
Status: RECRUITING
Last Update Posted: None
First Post: 2024-07-21

Brief Title: Percutaneous vs Conventional Radiofrequency Applications for the Treatment of Knee Osteoarthritic Pain
Sponsor: None
Organization: None

Study Overview

Official Title: Comparison of Percutaneous and Conventional Radiofrequency Applications for the Treatment of Knee Osteoarthritic Pain A Randomized Controlled Trial
Status: RECRUITING
Status Verified Date: 2024-07
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: This study aims to compare percutaneous and conventional radiofrequency applications for the treatment of knee osteoarthritic pain
Detailed Description: Osteoarthritis OA is a progressive degenerative joint disease that affects the joint cartilage and surrounding tissues It mostly affects the weight-bearing joints and in this respect the knee joint is one of the joints that is most affected

Radiofrequency RF treatment has been used for several painful conditions such as trigeminal neuralgia cancer pain and spinal pain To destroy nerves or disrupt the transmission of pain signals originally using producing heat lesions RF current is applied to the trigeminal ganglion the spinothalamic tracts of the spinal cord the medial branches of posterior rami and the dorsal root ganglion In addition to these there have been a few attempts to apply RF current for the treatment of painful conditions of joints of the extremities

Percutaneous radiofrequency ablation RFA of articular sensory nerves has recently emerged as an attractive and minimally invasive approach to treat chronic pain due to large-joint osteoarthritis in select patients

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