End Stage Renal Disease Clinical Trial
Official title:
Impact of Providing High Protein Bar to Dialysis Patients With Low Serum Albumin
NCT number | NCT00597025 |
Other study ID # | SR017PB |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2007 |
Est. completion date | December 2009 |
Verified date | April 2019 |
Source | Satellite Healthcare |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 375 |
Est. completion date | December 2009 |
Est. primary completion date | December 2009 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
United States | Satellite Healthcare, Inc. | Mountain View | California |
United States | WellBound, Inc. | Mountain View | California |
Lead Sponsor | Collaborator |
---|---|
Satellite Healthcare |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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. | ||
Primary | 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 | Proportion of patients who reached the goal albumin of >3.5 g/dL during the study period | Month 3 | ||
Secondary | 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 | ||
Secondary | Impact of protein intake on laboratory measures such as pre-albumin, CRP and ferritin will be monitored | Each month for 3 months |
Status | Clinical Trial | Phase | |
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