Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06555523
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-13
Brief Title:
Trigger Point Injection in Patients With Myofascial Pain Syndrome
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison of Trigger Point Injection Application Methods in Patients With Fibromyalgia Syndrome and Myofascial Pain Syndrome
Status:
RECRUITING
Status Verified Date:
2024-08
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 the effectiveness of blinded versus ultrasound-guided trigger point injections into the trapezius muscle in patients with FMS Seventy-five patients with FMS will participate in this study They will be randomly assigned to one of two groups one group received ultrasound-guided trigger point injections while the other group received blinded trigger point injections Both groups will follow the same home exercise regimen which included stretching and posture exercises targeting the trapezius and pectoral muscles The effectiveness of the treatments was evaluated one month post-treatment The assessment tools will include the Fibromyalgia Impact Questionnaire FIQ for function the Visual Analog Scale VAS for pain the Beck Anxiety Inventory Beck-A for anxiety and the Neck Disability Questionnaire NDQ for neck disability
Detailed Description:
The primary objectives in treating Fibromyalgia Syndrome FMS are to deactivate trigger points alleviate pain and remove factors that exacerbate the condition Recently the use of ultrasound US has been advocated to reduce potential complications during trigger point injections and to ensure more effective administration of the treatmentThis study aims to compare the effectiveness of blinded versus ultrasound-guided trigger point injections into the trapezius muscle in patients with FMS Seventy-five patients with FMS will participate in this study They will be randomly assigned to one of two groups one group received ultrasound-guided trigger point injections while the other group received blinded trigger point injections Both groups will follow the same home exercise regimen which included stretching and posture exercises targeting the trapezius and pectoral muscles The effectiveness of the treatments was evaluated one month post-treatment The assessment tools will include the Fibromyalgia Impact Questionnaire FIQ for function the Visual Analog Scale VAS for pain the Beck Anxiety Inventory Beck-A for anxiety and the Neck Disability Questionnaire NDQ for neck disability
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