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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03401944
Other study ID # MB1+2
Secondary ID
Status Completed
Phase N/A
First received December 21, 2017
Last updated January 22, 2018
Start date January 1, 2005
Est. completion date December 31, 2014

Study information

Verified date January 2018
Source Göteborg University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study investigates effects related to muscle protein metabolism at provision of Total Parenteral nutrition.


Description:

Randomized study investigating alterations in muscle protein metabolism at provision of parenteral nutrition. The study uses a genomic/transcriptomic/proteomic approach to evaluate factors related to activation of skeletal muscle protein synthesis. Patients scheduled for major gastrointestinal surgery are included. Muscle specimens are collected during surgery.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date December 31, 2014
Est. primary completion date December 31, 2014
Accepts healthy volunteers No
Gender All
Age group 20 Years to 85 Years
Eligibility Inclusion Criteria:

- Major gastrointestinal surgery

- Assumed need of post-operative artificial nutrition.

Exclusion Criteria:

- Insulin dependent diabetes

- Steroid medication

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
TPN

Other:
Control


Locations

Country Name City State
Sweden Department of Surgery Göteborg

Sponsors (1)

Lead Sponsor Collaborator
Göteborg University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle protein metabolism Alterations in muscle protein metabolism will be assessed by various standard techniques for gene and protein expression. Combined measurements of cell-signaling molecules representing anabolic and catabolic signaling pathways will be evaluated in relation to transcription of muscle myosin proteins. Single evaluation point at 12-14 hours following the start of overnight infusion.