Ignite Creation Date:
2024-05-06 @ 7:54 PM
Last Modification Date:
2024-10-26 @ 3:16 PM
Study NCT ID:
NCT06178562
Status:
TERMINATED
Last Update Posted:
2024-03-05
First Post:
2023-12-12
Brief Title:
Intermittent Oro-Esophageal Tube Feeding vs Nasogastric Tube Feeding in Infants With Pierre Robin Syndrome
Sponsor:
Zeng Changhao
Organization:
Peoples Hospital of Zhengzhou University
Study Overview
Official Title:
Improving Clinical Outcomes in Infants With Pierre Robin Syndrome A Randomized Controlled Study of Intermittent Oro-Esophageal Tube Feeding vs Nasogastric Tube Feeding
Status:
TERMINATED
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
ethical issues
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PRS
Brief Summary:
This was a randomized controlled study The infants enrolled were randomly divided into the IOE group with Intermittent Oro-Esophageal Tube Feeding n25 and the PNG group with Nasogastric Tube Feeding n23 all receiving systemic therapy Before and after 4-week treatment pulmonary infection swallowing function nutritional status and body weight between the two group were compared
Detailed Description:
Pierre Robin Syndrome PRS can cause dysphagia In China persistent nasogastric tube feeding PNG is the mainstream choice as nutrition support in the dysphagic infants with PRS However PNG is associated with various complications necessitating the exploration for a safer and more effective nutritional support approach Therefore this study aims to observe the clinical effect of intermittent oro-esophageal tube feeding IOE compared to PNG in the dysphagic infants with PRS who received systemic therapy
This was a randomized controlled study The infants enrolled were randomly divided into the IOE group with IOE n25 and the PNG group with PNG n23 all receiving systemic therapy Before and after 4-week treatment pulmonary infection swallowing function nutritional status and body weight between the two group were compared
This was a randomized controlled study The infants enrolled were randomly divided into the IOE group with IOE n25 and the PNG group with PNG n23 all receiving systemic therapy Before and after 4-week treatment pulmonary infection swallowing function nutritional status and body weight between the two group were compared
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