Ignite Creation Date:
2024-05-06 @ 8:17 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06328959
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-03-25
First Post:
2024-03-09
Brief Title:
Effect of Oral Feeding in Infants With Pierre Robin Syndrome
Sponsor:
Copka Sonpashan
Organization:
Chao Phya Abhaibhubejhr Hospital
Study Overview
Official Title:
Effect of Oral Feeding in Infants With Pierre Robin Syndrome 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:
This was a randomized controlled study The infants enrolled were randomly divided into the IOE group with Intermittent Oro-Esophageal Tube Feeding and the PNG group with Nasogastric Tube Feeding 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 and the PNG group with PNG 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 and the PNG group with PNG 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