NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000001425

Registered date:10/10/2008

A clinical study on micronutrients in the post-gastrointestinal surgery patients receiving parenteral nutrition

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedIn-patients received gastrointestinal surgery and requiring parenteral nutrition
Date of first enrollment2008/10/01
Target sample size16
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)administration period: 5 days Frequency of administration: every day administration period: 5 days Frequency of administration: every day Change the dose

Outcome(s)

Primary OutcomeBlood concentration/Urinary excretion
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude 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

Related Information

Contact

public contact
Name Ryoji Fukushima
Address 2-11-1, Kaga, Itabashi-ku, Tokyo Japan
Telephone 03-3964-1211
E-mail
Affiliation Teikyo University Hospital Department of surgery
scientific contact
Name Ryoji Fukushima
Address 2-11-1, Kaga, Itabashi-ku, Tokyo Japan
Telephone 03-3964-1211
E-mail
Affiliation Teikyo University Hospital Department of surgery