- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00497380
Arginine Feeding: a Novel Strategy to Improve Protein Metabolism in Cancer and the Response to Surgery
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In the present proposal, the effects of surgery and cancer will be examined by comparing subjects undergoing breast surgery because of malignancy vs. prophylactic reasons (aim 1). Furthermore, the effects of one-week pre-operative protein feeding with or without enrichment with arginine on post-operative protein metabolism (aim 2) will be investigated in the cancer group. Variables of interest are: 1. Whole-body and skeletal muscle protein metabolism, whole body arginine turnover and de-novo arginine production rate, and the anabolic capacity to feeding(assessed by stable isotope methodology). 2. Body weight, muscle mass and functional status, score for well-being (assessed by Profile of Mood State and Mini Mental State).
In the present study, we propose that a nutritional supplement that is high in protein content and enhanced in arginine will be more effective than a typical commercial nutritional supplement in diminishing the catabolic effects of surgery in subjects with cancer, thereby optimizing their quality of life. If this is found to be the case, this would provide the basis for reformulating the nutritional composition in accord with the effects of cancer and surgery on protein metabolism.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Arkansas
-
Little Rock, Arkansas, United States, 72205
- University of Arkansas for Medical Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Cancer groups (for aims 1 and 2)
- Recently diagnosed (up to 4 weeks prior to treatment for cancer) with stage I, II or III invasive breast cancer
- Undergoing mastectomy
- Age greater than 30 years
- Ability to sign informed consent
- Good performance status defined by ECOG scale 0,1 or 2 (see CRF performance status)
Control group (for aim 1)
- Age greater than 30 years
- Undergoing prophylactic mastectomy
- Ability to sign informed consent
- Good performance status defined by ECOG scale 0,1 or 2 (see CRF performance status)
Exclusion Criteria:
All groups (aim 1 and 2)
- Body weight loss of greater than 10% in the past 3 months
- Previous anti-cancer therapy (e.g. chemotherapy or radiotherapy) or surgery less than 4 weeks prior to the experiment
- Diagnosed diabetes type I or II
- Untreated metabolic diseases including liver or renal disease
- Any documented autoimmune disease
- Use of corticosteroids, beta-antagonists or nitrovasodilators
- Use of supplements enriched with amino acids
- Presence of acute illness or metabolically unstable chronic illness
- Unstable heart disease requiring therapy or recent myocardial infarction (less than 1 year)
- Current alcohol or drug abuse (ETOH more than 2 servings per day)
- Allergy/intolerance to any of the ingredients of the study products
- Any other condition deemed by the PI and the study physician as exclusion or that interferes with proper conduct of the study/ safety of the patient.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Arginine enriched nutrition
|
Oral nutritional supplement
|
|
Placebo Comparator: Nutrition
|
Oral nutritional supplement
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Net protein balance
Time Frame: end of study
|
end of study
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Arginine turnover
Time Frame: end of study
|
end of study
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nicolaas Deutz, M.D., Ph.D., University of Arkansas
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 81167
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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