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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01830907
Other study ID # First Hospital of JLU
Secondary ID
Status Completed
Phase Phase 0
First received April 10, 2013
Last updated April 11, 2013
Start date January 2012
Est. completion date March 2013

Study information

Verified date April 2013
Source First Hospital of Jilin University
Contact n/a
Is FDA regulated No
Health authority China: Ministry of HealthChina: Ethics Committee
Study type Interventional

Clinical Trial Summary

Evaluation of the impact of preoperative nutritional support on clinical outcomes in patients at nutritional risk. The primary endpoint was the complication rate and the second endpoint was the length of stay.


Recruitment information / eligibility

Status Completed
Enrollment 460
Est. completion date March 2013
Est. primary completion date February 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- clinical diagnosis of gastric cancer surgery preoperative stage

Exclusion Criteria:

- neoadjuvent chemoradiation

- pregnant

- advanced stage

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
carbohydrates

vitamins


Locations

Country Name City State
China First hospital of Jilin University Changchun Jilin

Sponsors (1)

Lead Sponsor Collaborator
First Hospital of Jilin University

Country where clinical trial is conducted

China, 

References & Publications (1)

van Stijn MF, Korkic-Halilovic I, Bakker MS, van der Ploeg T, van Leeuwen PA, Houdijk AP. Preoperative nutrition status and postoperative outcome in elderly general surgery patients: a systematic review. JPEN J Parenter Enteral Nutr. 2013 Jan;37(1):37-43. doi: 10.1177/0148607112445900. Epub 2012 May 1. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Infectious complication 30 days Yes
Secondary Length of hospital stay 30 days Yes
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