Ignite Creation Date:
2024-05-06 @ 3:22 PM
Last Modification Date:
2024-10-26 @ 1:48 PM
Study NCT ID:
NCT04608071
Status:
COMPLETED
Last Update Posted:
2020-11-02
First Post:
2020-10-27
Brief Title:
A Modified Method for Blind Bedside Placement of Post-pyloric Feeding Tube
Sponsor:
Second Affiliated Hospital School of Medicine Zhejiang University
Organization:
Second Affiliated Hospital School of Medicine Zhejiang University
Study Overview
Official Title:
Efficacy and Safety of a Modified Method for Blind Bedside Placement of Post-pyloric Feeding Tubea Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2020-04
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:
To compare efficacy and safety of a new modified post-pyloric feeding tube bedside catheterization with Corpak 10-10-10 protocol and electromagnetic guided catheterization for treatment of patients with dysphagia and at high-risk of aspiration pneumonia We conducted a single-center single-blinded and randomized controlled clinical trial A total of 63 patients were treated with the non-gravity type CORFLO gastrointestinal feeding tube between 20171 and 20191 using different procedures in the M group patients underwent modified post-pyloric feeding tube bedside placement in C group patients underwent conventional Corpak protocol in EM group patients received standard electromagnetic guided tube placement
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