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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00179179
Other study ID # 50189
Secondary ID R01DK045604
Status Completed
Phase Phase 2
First received September 13, 2005
Last updated July 8, 2009
Start date April 2005
Est. completion date May 2007

Study information

Verified date July 2009
Source Vanderbilt University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To test the hypothesis that an exercise session combined with adequate nutritional supplementation improves skeletal muscle protein accretion during a hemodialysis session.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date May 2007
Est. primary completion date May 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- On hemodialysis for more than 3 months, on a thrice weekly hemodialysis program.

- Adequately dialyzed (Kt/V > 1.2).

- Age 18-75

Exclusion Criteria:

- Pregnant women.

- Patients unable to perform exercise

- 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 malfunctioning arterial-venous access (recirculation and/or blood flow < 750 ml/min)

- Patients receiving steroids and/or other immunosuppressive agents.

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
nutritional supplementation
2 oral ingestions per study visit of protein supplement containing a total of 960 kilocalories: 132.8 kilocalories from protein, 412.8 kilocalories from carbohydrates, and 412.8 kilocalories from fat; 6 study visits over a 12-month period
Behavioral:
exercise
resistance training on a duel leg press consisting of 3 sets of 8-12 repetitions; the first 5 study visits over a 12-month period

Locations

Country Name City State
United States Vanderbilt University Medical Center Nashville Tennessee

Sponsors (1)

Lead Sponsor Collaborator
Vanderbilt University

Country where clinical trial is conducted

United States, 

Outcome

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