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Effects of individualized nutrition management scheme for patients with dysphagia after stroke

Construction and effect evaluation of individualized nutrition management scheme for patients with dysphagia after stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054054
Enrollment
Unknown
Registered
2021-12-08
Start date
2020-09-01
Completion date
Unknown
Last updated
2022-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysphagia after stroke

Interventions

Control Group:Patients with drinking water grade II of Kubota should take food by mouth
patients with drinking water grade III-IV should indwell gastric tube or eat by mouth
patients with drinking water grade V should be indwelled gastric tube according to the doctor's advice
Intervention Group:Patients with drinking water grades II-III used V-VST assessment for dietary preparation and eating. Patients with drinking water grades IV and V were given intermittent oral-esopha

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
29 Years to 88 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Patients diagnosed with ischemic stroke or hypertensive intracerebral hemorrhage, in line with the diagnostic criteria revised by the Fourth National Cerebrovascular Disease Conference, and confirmed by head CT or MRI; 3. Glasgow Coma Scale (GCS) >= 13 points; 4. Low-water field drinking water test >= grade 2; 5. NRS2002 >= 3 points.

Exclusion criteria

Exclusion criteria: 1. Patients with previous abnormal swallowing; 2. Patients with significantly abnormal gastrointestinal function, frequent vomiting or diarrhea, or patients with contraindications to enteral nutrition; 3. Patients who have received enteral nutrition support before admission; 4. Poor compliance, unable to complete the follow-up, incomplete clinical data, and other researchers who think it is not suitable for enrollment; 5. Patients and immediate family members are unwilling to join the group.

Design outcomes

Primary

MeasureTime frame
swallowing function;

Secondary

MeasureTime frame
total serum protein;serum albumin;hemoglobin;skeletal muscle content;body fat rate;average length of stay;hospitalization expenses;

Countries

China

Contacts

Public ContactYan Xiuli

Department of Neurology, the First Hospital of Jilin University

yanxiuli2008@126.com+86 15843079660

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026