Ignite Creation Date:
2024-05-06 @ 6:11 PM
Last Modification Date:
2024-10-26 @ 2:43 PM
Study NCT ID:
NCT05572931
Status:
COMPLETED
Last Update Posted:
2024-02-20
First Post:
2022-10-02
Brief Title:
Effect of Fus Subcutaneous Needling on Postoperative Acute Pain in Patients With Lumbar Spine Surgery
Sponsor:
China Medical University Hospital
Organization:
China Medical University Hospital
Study Overview
Official Title:
Effect of Fus Subcutaneous Needling on Postoperative Acute Pain in Patients With Lumbar Spine Surgery a Single-blinded Randomized Control Study
Status:
COMPLETED
Status Verified Date:
2024-02
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 goal of this clinical trial is to evaluate Fus Subcutaneous Needling FSN in postoperative pain in patients with Lumbar Spine Surgery LSS The main questions it aims to answer are
Is FSN effective for postoperative pain
Dose FSN decrease the tissue hardness after LSS
Dose FSN have the effect of anti-inflammatory after LSS
Participants will receive routine analgesic and FSN after LSS Researchers will compare Sham group to see if FSN being effective for postoperative pain
Is FSN effective for postoperative pain
Dose FSN decrease the tissue hardness after LSS
Dose FSN have the effect of anti-inflammatory after LSS
Participants will receive routine analgesic and FSN after LSS Researchers will compare Sham group to see if FSN being effective for postoperative pain
Detailed Description:
None
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