Viewing Study NCT06303973



Ignite Creation Date: 2024-05-06 @ 8:13 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06303973
Status: COMPLETED
Last Update Posted: 2024-03-12
First Post: 2024-03-05

Brief Title: Effect of Oral Enteral Nutrition in Pierre Robin Syndrome
Sponsor: Muhammad
Organization: Ahmadu Bello University Teaching Hospital

Study Overview

Official Title: Effect of Oral Versus Nasal Enteral Nutrition in Pierre Robin Syndrome A Randomized Controlled Study
Status: COMPLETED
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 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

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