Sign in

NCT06328894Completed

Effect of Different Feeding Modes on Psychological Condition and Experience in Stroke Patients

A Randomized Controlled Trial to Explore the Effect of Different Feeding Modes on Psychological Condition and Experience in Stroke Patients

Source: ClinicalTrials.gov · Last updated 8 May 2026

Brief summary (registry, in English)

The goal of this clinical trial is to compare the differences on Psychological Condition and Experience in ischemic stroke patients using Intermittent Oro-esophageal Tube and Nasogastric Tube. Patients will be randomly divided into an observation group and a control group, all receiving routine rehabilitation treatment. On this basis, the observation group will use Intermittent Oro esophageal Tube for enteral nutrition support, while the control group will use Nasogastric Tube. Researchers will compare Psychological Condition and Experience of two groups.

Status (registry)
Completed
Study type
Interventional
Enrollment
156 (actual)
First submitted
10 Mar 2024
Start date
27 Mar 2024
Primary completion date
8 Jun 2025
Lead sponsor
Zeng Xi
Diseases
Stroke
NCT number
NCT06328894

What you commit to

  • Study type: Interventional
  • Participants enrolled: 156
  • From 27 Mar 2024 to the primary completion date, 8 Jun 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Simultaneously in need to undergo other therapy that might affect the outcomes of this study.

Other illness

  • Dysphagia that might be caused by other diseases that might cause dysphagia, such as head and neck tumors, traumatic brain injury, myasthenia gravis, etc.
  • Complicated with severe liver and kidney failure, tumors, or hematological disorders.

Other

  • Pregnant or nursing females.

Who the study is looking for

  • Age\>18 years.
  • Meeting the diagnostic criteria for ischemic stroke .
  • Dysphagia confirmed by Videofluoroscopic Swallowing Study.
  • Clear consciousness.
  • Stable vital signs.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Department of rehabilitation medicine, the first ZU hospital north campus
Coordinator of this site? Confirm its status
ZhenzhouChinaUnknown status
Department of rehabilitation medicine, the first ZU hospital western campus
Coordinator of this site? Confirm its status
ZhenzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.