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Oro-esophageal vs Nasogastric Tube Feeding in Ischemic Stroke with Dysphagia: A Protocol

Oro-esophageal vs Nasogastric Tube Feeding in Ischemic Stroke with Dysphagia: A Protocol
Photo by CDC / Unsplash
Key Takeaway
Note that this is a protocol; no results are available to guide clinical decisions on tube feeding in ischemic stroke with dysphagia.

This is a protocol for a multicenter randomized controlled trial that will enroll 422 ischemic stroke patients with dysphagia who require tube feeding. The intervention is oro-esophageal tube feeding, compared with standard nasogastric tube feeding. The primary outcome is dysphagia severity measured by the Dysphagia Outcome and Severity Scale (DOSS). Secondary outcomes include time to improvement of one level from baseline DOSS, time to oral intake, accumulation of secretions (Murray Secretion Scale), pharyngeal residue (Yale Pharyngeal Residual Severity Rating Scale), airway protection (Penetration-Aspiration Scale), and aspiration symptoms. Follow-up for aspiration symptoms is 6 weeks. Safety data such as adverse events, serious adverse events, discontinuations, and tolerability are not reported in this protocol. Limitations include that this is a protocol only; no results are available. The study aims to provide evidence-based support for the effects of tube feeding on swallowing-related rehabilitation outcomes. Clinicians should await results before changing practice.

Study Details

Study typeRct
EvidenceLevel 2
PublishedApr 2026
View Original Abstract ↓
BackgroundEnteral nutrition is commonly practiced for ischemic stroke survivors with dysphagia. In Eastern Asia, nasogastric and oro-esophageal tubes are the mainstream options. However, there is a lack of rigorous clinical evidence on the effects of these two feeding methods on swallowing-related rehabilitation outcomes and clinical relevance.ObjectivesThis study is clinically oriented and aims to assess the effect of nasogastric versus oro-esophageal tube feeding on the degree and speed of dysphagia improvement, and aspiration symptoms.MethodsThis multicenter randomized controlled trial will include 422 ischemic stroke patients with dysphagia who require tube feeding. Stratified randomization will be performed to assign participants 1:1 to the oro-esophageal or nasogastric groups. All participants will receive 15-days routine rehabilitation care and nasogastric or oro-esophageal feeding, according to their group assignment.OutcomesThe primary outcome is the dysphagia severity assessed using the Dysphagia Outcome and Severity Scale (DOSS). The secondary outcomes include time to improvement of one level from the baseline DOSS, time to oral intake, accumulation of secretions assessed using the Murray Secretion Scale, pharyngeal residue after swallowing assessed using the Yale Pharyngeal Residual Severity Rating Scale, and airway protection assessed using the Penetration-Aspiration Scale. Aspiration symptoms will be monitored for 6 weeks.DiscussionThis study aims to provide evidence-based support for the comprehensive effects of tube feeding on swallowing-related rehabilitation outcomes.Clinical trial registrationClinicalTrials.gov, identifier NCT07386834.
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