Ignite Creation Date:
2024-05-06 @ 7:03 PM
Last Modification Date:
2024-10-26 @ 3:00 PM
Study NCT ID:
NCT05888285
Status:
COMPLETED
Last Update Posted:
2023-06-05
First Post:
2023-05-15
Brief Title:
Erector Spina Plane Block and Radiofrequency Treatmen
Sponsor:
Diskapi Teaching and Research Hospital
Organization:
Diskapi Teaching and Research Hospital
Study Overview
Official Title:
Is Radiofrequency Necessary in Myofascial Pain
Status:
COMPLETED
Status Verified Date:
2023-06
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:
ESP is the deepest back muscle originating from the transverse processes of the vertebrae Blocks applied to this region are effective for a longer time and in the broader area than those applied to superficial muscles Recently pulsed radiofrequency treatments have also been performed in myofascial pain and successful results have been obtained The investigators aim to investigate whether there is a difference between these two applications in terms of treatment efficacy
Detailed Description:
Trigger point injections and erector spina planus muscle ESP blocks are used to treat back pain related to myofascial pain syndrome ESP is the deepest back muscle originating from the transverse processes of the vertebrae Blocks applied to this region are effective for a longer time and in the broader area than those applied to superficial muscles Recently pulsed radiofrequency treatments have also been performed in myofascial pain and successful results have been obtained
Deep and superficial back muscles transverse processes of the vertebrae costume and pleural movement are identified by ultrasonographic examination The investigators perform the intervention through the transverse processes The investigators give 20 ccs of fluid bupivacaine steroids saline The patients to whom The investigators apply pulsed radiofrequency complete the procedure by giving 20 ccs of fluid after the radiofrequency application on the transverse processes and during the procedure using 10 cm 21 gauge radiofrequency needles with an active tip of 10 mm The radiofrequency wave is applied at 2 Hz ten milliseconds and 55 volts for 55 for 10 minutes
The investigators aim to investigate whether there is a difference between these two applications in terms of treatment efficacy For this reason the Visual Pain Scale of each patient will be recorded before the procedure the second week after the procedure and the first month The Centrality of Pain Scale will be applied to these patients at the controls The correlation between the results of this scale which evaluates the emotional and physical state of the patients and the post-treatment pain scales will be evaluated
Deep and superficial back muscles transverse processes of the vertebrae costume and pleural movement are identified by ultrasonographic examination The investigators perform the intervention through the transverse processes The investigators give 20 ccs of fluid bupivacaine steroids saline The patients to whom The investigators apply pulsed radiofrequency complete the procedure by giving 20 ccs of fluid after the radiofrequency application on the transverse processes and during the procedure using 10 cm 21 gauge radiofrequency needles with an active tip of 10 mm The radiofrequency wave is applied at 2 Hz ten milliseconds and 55 volts for 55 for 10 minutes
The investigators aim to investigate whether there is a difference between these two applications in terms of treatment efficacy For this reason the Visual Pain Scale of each patient will be recorded before the procedure the second week after the procedure and the first month The Centrality of Pain Scale will be applied to these patients at the controls The correlation between the results of this scale which evaluates the emotional and physical state of the patients and the post-treatment pain scales will be 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