A Clinical Study to Evaluate the Clinical Outcomes of Hepatectomy With Nutritional Risk After Preoperative Nutritional Support
NCT ID: NCT01292330
Last Updated: 2011-02-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2010-01-31
2011-11-30
Brief Summary
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Study design:
1.Prospective，randomized, controlled clinical study;2.Patients: The subjects were from Peking Union Medical College Hospital (PUMCH).
Study arrangement:
1. The collection of patients with selected standard
2. Preoperative evaluation included nutritional status,liver function and tumor characteristics
3. The experimental group received Preoperative Nutritional Support for 4 days,the control group got nothing
4. Both groups received conventional therapy after operation
5. The comparation of the clinical outcomes in both groups
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Interventions
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nutritional support before operation
nutritional support before operation for more than 4 days
Eligibility Criteria
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Inclusion Criteria
2. Nutritional Risk Screening 2002(NRS-2002) was Greater or equal 3 points with in 24 hours after admission
18 Years
90 Years
ALL
No
Sponsors
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Peking Union Medical College Hospital
OTHER
Responsible Party
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Peking Union Medical College Hospital
Locations
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Yilei Mao
Beijing, Beijing Municipality, China
Countries
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Facility Contacts
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References
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Lu X, Li Y, Yang H, Sang X, Zhao H, Xu H, Du S, Xu Y, Chi T, Zhong S, Yu K, Mao Y. Improvement of nutritional support strategies after surgery for benign liver tumor through nutritional risk screening: a prospective, randomized, controlled, single-blind clinical study. Hepatobiliary Surg Nutr. 2013 Feb;2(1):14-21. doi: 10.3978/j.issn.2304-3881.2012.11.04.
Other Identifiers
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PUMCH-Liver surgery -Nutrition
Identifier Type: -
Identifier Source: org_study_id
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