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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 NCT06267950
Study type Interventional
Source People's Hospital of Zhengzhou University
Contact Qianyun Lu, Master
Phone 15333866454
Email luqianyun@126.com
Status Recruiting
Phase N/A
Start date February 29, 2024
Completion date October 2024

See also
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Completed NCT02658318 - Postoperative Complications After Cleft Palate Closure in Patients With Pierre Robin Sequence: Operative Considerations N/A
Completed NCT06303973 - Effect of Oral Enteral Nutrition in Pierre Robin Syndrome N/A
Completed NCT02266043 - Early Treatment Outcomes in Pierre-Robin-Like Phenotype