In-patients received gastrointestinal surgery and requiring parenteral nutrition
Conditions
Interventions
administration period: 5 days Frequency of administration: every day
administration period: 5 days Frequency of administration: every day Change the dose
Sponsors
Department of surgery, Teikyo University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Patients schedulled for gastorectomy or colorectomy (2) Patients providing written informed consent (3) Patients not youger than 20 years old (at the time of informed consent)
Exclusion criteria
Exclusion criteria: (1) Patients with an abnormal electrolyte metabolism (2) Patients with a congestive heart failure (3) Patients with a serious liver failure (hepatic coma or possible hepatic coma) (4) Patients with a serious kidney failure or azotemia (5) Patients with an abnormal amino acid metabolism (6) Patients with a severe acidosis (7) Patients with a decreased urine volume due to the obstructive uropathy (8) Patients with with a disease histry of hypersensitivity to the ingredients of intravenous solution (9) Others who are deemed unsuitable for inclusion in the study for any other reason based on the assessment by the investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood concentration/Urinary excretion | — |
Countries
Japan
Contacts
Public ContactRyoji Fukushima
Teikyo University Hospital Department of surgery
Outcome results
None listed