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Prognostic study of nutritional intervention by Gastrostomy in ALS patients

Prognostic study of nutritional intervention by Gastrostomy in ALS patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016626
Enrollment
Unknown
Registered
2018-06-13
Start date
2018-06-13
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

ALS, amyotrophic lateral sclerosis

Interventions

Group 1:Abbott Ensure Complete
Group 2:Megestrol

Sponsors

Dahua Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Participants diagnosed as familial or sporadic ALS, according to the World Federation of Neurology Standards; (2) male or female participants aged 18-70 years; (3) Participants must be able to provide informed consent and follow the test procedure; (4) Participants must have qualified nursing staff to assist in tube feeding; (5) The participants receiving the gastric fistula or stoma tube must be able to receive tube feeding; (6) The subjects were able to carry out non-invasive ventilation for less than 10 hours a day.

Exclusion criteria

Exclusion criteria: (1) Patients with unstable mental illness, including mental depression; (2) Women during pregnancy and who breastfeed after pregnancy; (3) History of hepatitis, including Nonalcoholic steatohepatitis (NASH), cholecystectomy, previous biliary diseases such as gallstones, diabetes, previous myocardial infarction, stroke and thromboembolism, liver and kidney insufficiency, breast tumor, uterine fibroids, hypertension, galactose or hyperglycemia patients; (4) Laboratory examination value: Alanine transaminase (ALT) or aspartate transaminase (AST) is greater than the normal range of 2.2 times or total bilirubin greater than the normal limit of twice times; (5) allergic to soybeans, fish or dairy products; (6) intolerance of nutritional supplements.

Design outcomes

Primary

MeasureTime frame
mRNA expression;

Countries

China

Contacts

Public ContactCAO JUN

Dahua Hospital

juncao11@sina.com+86 13611890000

Outcome results

None listed

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