Ignite Creation Date:
2024-05-06 @ 8:13 PM
Last Modification Date:
2024-10-26 @ 3:22 PM
Study NCT ID:
NCT06290791
Status:
COMPLETED
Last Update Posted:
2024-03-04
First Post:
2024-02-27
Brief Title:
Does a Drain Tube Influence the Postoperative Epidural Haematoma for Lumbar Biportal Endoscopic Surgery
Sponsor:
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Organization:
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Study Overview
Official Title:
Does a Drain Tube Influence the Postoperative Epidural Haematoma for Lumbar Biportal Endoscopic Surgery A Randomized Controlled Trial
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 purpose of this study was to evaluate if wound drains could influence postoperative spinal epidural hematoma POSEH in biportal endoscopic spinal surgery BESS procedures for decompression of lumbar spinal stenosis
Detailed Description:
How to reduce the rate of POSEH after lumbar spinal surgery is an obvious concern for spine surgeon Wound drains were recognized as effective methods and typically used to prevent the development of symptomatic epidural hematomas after spinal surgery However whether range prophylactic postoperative drainage after spinal decompression for the prevention of POSEH is still controversial Although there have been many studies focusing on the potential associations between wound drains and POSEH after lumbar spinal surgery a prospective study focusing on the role of drains in minimally invasive surgery of BESS for lumbar spinal decompression has been rare In present study our team sought to investigate the influence of wound drains for POSEH and provide clinical evidence for the selection of drainage in BESS procedures for the decompression of lumbar spinal stenosis
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