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Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06328959
Study type Interventional
Source Chao Phya Abhaibhubejhr Hospital
Contact Qianyun Ce
Phone 15333866454
Email zengxizdyfy@126.com
Status Not yet recruiting
Phase N/A
Start date March 2024
Completion date December 2024

See also
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Completed NCT06303973 - Effect of Oral Enteral Nutrition in Pierre Robin Syndrome N/A
Completed NCT02266043 - Early Treatment Outcomes in Pierre-Robin-Like Phenotype
Recruiting NCT06267950 - Effect of Oral Feeding in Infants With Pierre Robin Syndrome N/A