Unique ID issued by UMIN | UMIN000001425 |
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Receipt number | R000001714 |
Scientific Title | A clinical study on micronutrients in the post-gastrointestinal surgery patients receiving parenteral nutrition |
Date of disclosure of the study information | 2008/10/10 |
Last modified on | 2009/11/17 09:53:50 |
A clinical study on micronutrients in the post-gastrointestinal surgery patients receiving parenteral nutrition
A clinical study on micronutrients in the post-gastrointestinal surgery patients receiving parenteral nutrition
A clinical study on micronutrients in the post-gastrointestinal surgery patients receiving parenteral nutrition
A clinical study on micronutrients in the post-gastrointestinal surgery patients receiving parenteral nutrition
Japan |
In-patients received gastrointestinal surgery and requiring parenteral nutrition
Gastrointestinal surgery |
Others
NO
To investigate the micronutrients in the patients received gastrointestinal surgery and requiring parenteral nutrition
Efficacy
Exploratory
Pragmatic
Not applicable
Blood concentration/Urinary excretion
Interventional
Parallel
Randomized
Individual
Open -no one is blinded
Dose comparison
NO
NO
Institution is considered as a block.
YES
Central registration
2
Treatment
Medicine |
administration period: 5 days
Frequency of administration: every day
administration period: 5 days
Frequency of administration: every day
Change the dose
20 | years-old | <= |
Not applicable |
Male and Female
(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)
(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
16
1st name | |
Middle name | |
Last name | Ryoji Fukushima |
Teikyo University Hospital
Department of surgery
2-11-1, Kaga, Itabashi-ku, Tokyo
03-3964-1211
1st name | |
Middle name | |
Last name | Ryoji Fukushima |
Teikyo University Hospital
Department of surgery
2-11-1, Kaga, Itabashi-ku, Tokyo
03-3964-1211
Department of surgery, Teikyo University Hospital
Otsuka Pharmaceutical Factory, Inc.
Profit organization
NO
2008 | Year | 10 | Month | 10 | Day |
Unpublished
Completed
2008 | Year | 08 | Month | 21 | Day |
2008 | Year | 10 | Month | 01 | Day |
2009 | Year | 09 | Month | 01 | Day |
2008 | Year | 10 | Month | 10 | Day |
2009 | Year | 11 | Month | 17 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001714
Research Plan | |
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