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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00244075
Other study ID # 9458
Secondary ID
Status Completed
Phase Phase 2
First received October 21, 2005
Last updated May 22, 2015
Start date July 1998
Est. completion date August 2006

Study information

Verified date May 2015
Source Vanderbilt University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The goal of this study is to evaluate the metabolic effects of concomitant use of three consecutive doses of recombinant human growth hormone over three days and exercise during continuous nutrient infusion in chronic hemodialysis patients. We would also like to evaluate the metabolic effects of nutritional supplementation alone without the additional anabolic strategies.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date August 2006
Est. primary completion date August 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- On hemodialysis for more than 6 months, on a thrice weekly hemodialysis program;

- Adequately dialyzed (Kt/V > 1.4).

Exclusion Criteria:

- Patients unable to perform exercise.

- Pregnant women.

- Severe unstable underlying disease besides commonly associated with ESRD. Cardiac patients that are stable will be included.

- Patients hospitalized within the last month prior to the study.

- Patients with recirculation detected on the AV graft.

- Patients receiving steroids and/or other immunosuppressive agents

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
nutritional supplement
either oral nutritional formula (Nepro) or intravenous IDPN solution will be administered during hemodialysis; Nepro has a total calorie amount as well as protein, carbohydrate and fat content that are comparable to that of IDPN, and will be provided at four equal amounts with 1-hour intervals throughout the study (150 ml for a total of 600 ml over 4 hours of hemodialysis); IDPN consists of 225 ml of amino acids at a concentration of 15%, 112.5 ml of dextrose at 50% and 112.5 ml of lipids at 20%, will be given at a rate of 150 ml/hr, and will provide 209 kcal/hr
Drug:
recombinant human growth hormone (rcGH)
subcutaneous administration of 75 micrograms/kg/day of rcGH for 3 consecutive days
Behavioral:
exercise
either dual leg press (3 sets of 8-12 repetitions) beginning 30 minutes prior to hemodialysis, or modified stepper (minimum of 15 minutes up to a maximum of 90 minutes, depending upon the patient's tolerance) beginning 15 minutes post initiation of hemodialysis

Locations

Country Name City State
United States Vanderbilt University Nashville Tennessee

Sponsors (1)

Lead Sponsor Collaborator
Vanderbilt University

Country where clinical trial is conducted

United States, 

References & Publications (3)

Ikizler TA, Pupim LB, Brouillette JR, Levenhagen DK, Farmer K, Hakim RM, Flakoll PJ. Hemodialysis stimulates muscle and whole body protein loss and alters substrate oxidation. Am J Physiol Endocrinol Metab. 2002 Jan;282(1):E107-16. — View Citation

Pupim LB, Flakoll PJ, Ikizler TA. Nutritional supplementation acutely increases albumin fractional synthetic rate in chronic hemodialysis patients. J Am Soc Nephrol. 2004 Jul;15(7):1920-6. — View Citation

Pupim LB, Flakoll PJ, Levenhagen DK, Ikizler TA. Exercise augments the acute anabolic effects of intradialytic parenteral nutrition in chronic hemodialysis patients. Am J Physiol Endocrinol Metab. 2004 Apr;286(4):E589-97. Epub 2003 Dec 16. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary net muscle protein balance 10 hours No
Secondary net whole body protein balance 10 hours No
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