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Impact of Providing High Protein Bar to Dialysis Patients With Low Serum Albumin

Impact of Providing High Protein Bar to Dialysis Patients With Low Serum Albumin

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00597025
Enrollment
375
Registered
2008-01-17
Start date
2007-12-31
Completion date
2009-12-31
Last updated
2020-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End Stage Renal Disease, Hypoalbuminemia, Malnutrition

Keywords

Malnutrition, Hypoalbuminemia, Dietary Supplements, Hemodialysis, Peritoneal Dialysis

Brief summary

This study is to evaluate the impact of providing high protein supplementation in the form of a medical food bar containing 20grams of protein eath to hypoalbuminemic dialysis patients.

Interventions

DIETARY_SUPPLEMENTProtein Food Bar Intelligent Indulgence

Patients will be given one protein bar at each dialysis treatment, 3 times per week for 3 months

Sponsors

Satellite Healthcare
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subjects with ESRD undergoing center hemodialysis or peritoneal dialysis for more than 90 days. * 18 years of age or older. * Must have a reasonable expectation of remaining on treatment for at least 3 months. * Must have an average serum albumin of \<3.5 g/dL over the three months prior to entry into the study. * Must be able to understand and sign the informed consent. * Must be willing and able to participate in nutrition interviews for determination of nutrient intake from conventional foods.

Exclusion criteria

* Allergy to protein, milk, nuts or wheat. * Documented ongoing acute infection or inflammatory process including treatment with antibiotics within a two week time of study entry. * Severe acidosis defined as pre-dialysis serum bicarbonate levels of \<15 mEq/L. * Presence of conditions that would affect normal response to repletion of protein and calories, such as gastrointestinal disorders including inflammatory bowel disease. * Hospitalization for an infectious condition within 4 weeks prior to study entry. * Planned surgery within the three month study period including planned kidney transplantation.

Design outcomes

Primary

MeasureTime frame
The mean change (from baseline to month 3) in serum albumin levels among study groups and the proportion of patients treated with the protein food bar reaching an increase of 0.3 g/dL over the three month study period.Each month for the three months.
Incidence of potential adverse events including nausea, vomiting, diarrhea, acidosis, and uremic symptoms as evidenced by clinical symptoms and possible worsening of laboratory measures such as BUN, Kt/V, nPNA and bicarbonate.Each month for 3 months

Secondary

MeasureTime frame
Proportion of patients who reached the goal albumin of >3.5 g/dL during the study periodMonth 3
Overall acceptance and compliance of bar form medical food over a 3 month period will be assessed via the proportion of patients who ingested 75% or more of the recommended bars.Each month for 3 months
Impact of protein intake on laboratory measures such as pre-albumin, CRP and ferritin will be monitoredEach month for 3 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026