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NCT04259307Completed

Effect of Intensive Nutritional Support in Subacute Stroke Patient

Effect of Intensive Nutritional Support on Functional Recovery in Subacute Stroke Patient

Source: ClinicalTrials.gov · Last updated 7 Mar 2024

Brief summary (registry, in English)

Proper nutritional support during early rehabilitation may be beneficial for functional improvements in gaining functional independence and preventing complications in stroke patients. However, there was no consensus of proper amount of nutritional support in stroke patients. In this study, the investigators aimed to clarigy the effects of the intensive nutritional support during comprehensive rehabilitation during subacute phase to improve function in patients with first-ever strokes.

Status (registry)
Completed
Study type
Interventional
Enrollment
97 (actual)
First submitted
4 Feb 2020
Start date
29 Jan 2020
Primary completion date
31 Aug 2023
Lead sponsor
Samsung Medical Center
Diseases
Stroke
NCT number
NCT04259307

What you commit to

  • Study type: Interventional
  • Participants enrolled: 97
  • From 29 Jan 2020 to the primary completion date, 31 Aug 2023
  • 1 site 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, not your situation.

Who cannot take part

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

Other illness

  • Transient ischemic stroke
    • Progressive or unstable stroke
    • Pre-existing and active major neurological disease, e.g., spinal cord injury, Parkinson's disease, et al.
    • Pre-existing and active (e.g., on chronic medication) major psychiatric disease, such as major depression, schizophrenia, bipolar disease or dementia ⑤ Advanced liver, kidney, cardiac, or pulmonary disease, e.g., advanced hepatocellular carcinoma, end-stage renal failure, et al.)
    • A terminal medical diagnosis consistent with survival \< 1 year
    • Diabetes mellitus, Hyperlipidemia, Metabolic syndrome, Heart failure) ⑧ Pregnant or lactating women ⑨ Prohibited from taking medication (Omapone Peri 724mL or Winuf Peri 654mL)

Who the study is looking for

  • Acute first-ever stroke patients less than 7 days after onset
    • more than 19 years old at stroke onset ③ stroke confirmed by brain CT or MRI
    • body mass index (BMI) \<25 before the comprehensive rehabilitation ⑤ Mini Nutritional Assessment \< 12 before the comprehensive rehabilitation ⑥ Fugl-Meyer assessment \< 85 at 7 days after stroke onset

Age in the registry: 19 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Samsung Medical Center
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

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