Viewing Study NCT04806360



Ignite Creation Date: 2024-05-06 @ 3:55 PM
Last Modification Date: 2024-10-26 @ 2:00 PM
Study NCT ID: NCT04806360
Status: UNKNOWN
Last Update Posted: 2022-05-09
First Post: 2021-02-16

Brief Title: Anterior Spinal Canal Reconstruction and Fusion Surgery for Treating Degenerative Cervical Kyphosis With Stenosis
Sponsor: Shanghai Changzheng Hospital
Organization: Shanghai Changzheng Hospital

Study Overview

Official Title: Application of Anterior Spinal Canal Reconstruction and Fusion Surgery for Treating Degenerative Cervical Kyphosis With Stenosisa Multicenter Randomized Controlled Trial
Status: UNKNOWN
Status Verified Date: 2022-05
Last Known Status: NOT_YET_RECRUITING
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: Degenerative cervical kyphosis with stenosis DCKS is a common cervical spine degenerative disease causing pain numbness and weakness of limbs which seriously affect the quality of life of the patient Surgery is an effective way to treat this condition however the best surgical procedure is still controversial Anterior spinal canal reconstruction and fusion surgery ACRF is a new surgical procedure that previously proposed by our team it combines the advantages of both the conventional anterior and posterior approach The purpose of this study is to evaluate the safety and effectiveness of ACRF surgery for treating DCKS A multicenter prospective randomized controlled trial was designed Eligible patients will be randomly divided into three groups including the ACRF group the conventional anterior surgery group and the conventional posterior surgery group Demographic data surgery Information and follow-up results will be collected and compared between groups
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