Ignite Creation Date:
2024-05-06 @ 8:16 PM
Last Modification Date:
2024-10-26 @ 3:23 PM
Study NCT ID:
NCT06312371
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-03-15
First Post:
2024-03-08
Brief Title:
Intermittent Oro-esophageal Tube on Feeding Hesitancy in Stroke Patients
Sponsor:
Muhammad
Organization:
Ahmadu Bello University Teaching Hospital
Study Overview
Official Title:
Intermittent Oro-esophageal Tube on Feeding Hesitancy in Stroke Patients A Randomized Controlled Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-03
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 aim of this clinical trial is to compare Feeding Hesitancy of ischemic stroke patients who receive enteral nutrition support through either Intermittent Oro-esophageal Tube or Nasogastric Tube Patients will be randomly assigned to either an observation group or a control group with both groups receiving routine rehabilitation treatment The observation group will receive enteral nutrition support through Intermittent Oro-esophageal Tube while the control group will receive it through Nasogastric Tube Researchers will then compare Feeding Hesitancy of the two groups
Detailed Description:
The study will last 15 days for each participant The aim of this clinical trial is to compare Feeding Hesitancy of ischemic stroke patients who receive enteral nutrition support through either Intermittent Oro-esophageal Tube or Nasogastric Tube Patients will be randomly assigned to either an observation group or a control group with both groups receiving routine rehabilitation treatment The observation group will receive enteral nutrition support through Intermittent Oro-esophageal Tube while the control group will receive it through Nasogastric Tube Researchers will then compare Feeding Hesitancy of the two groups
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