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DaVita Assessment of Nutritional Supplement Effects (DANSE)

DaVita Assessment of Nutritional Supplement Effects

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00895401
Acronym
DANSE
Enrollment
160
Registered
2009-05-08
Start date
2009-04-30
Completion date
Unknown
Last updated
2011-02-08

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

Conditions

Malnutrition

Keywords

Nutritional supplement, Malnutrition, Hemodialysis, Nepro with Carb Steady

Brief summary

This is a Phase IV randomized controlled study assessing the effectiveness of a commercially available nutritional supplement on malnourished prevalent hemodialysis patients. Patients will be randomized to either receive one can of Nepro with Carb Steady at each dialysis treatment for 6 months or to receive the standard of care counseling for malnutrition. The primary hypothesis is that hypoalbuminemic maintenance hemodialysis patients will demonstrate an improvement in albumin levels with oral nutritional supplement provided in-center thrice weekly in addition to standard of care as compared to malnourished maintenance hemodialysis patients provided standard of care alone.

Interventions

DIETARY_SUPPLEMENTNepro with Carb Steady

Nepro with Carb Steady is a commercially available renal specific oral nutritional supplement designed to meet the nutrient needs of dialysis patients. The supplement is 8 oz and provides 425 kcal and 19 grams of protein.

OTHERStandard of Care

Standard of Care for malnourished maintenance hemodialysis patients

Sponsors

Abbott Nutrition
CollaboratorINDUSTRY
Davita Clinical Research
Lead SponsorINDUSTRY

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

* Patient is at least 18 years of age * Patient has been on hemodialysis \>6 months at the time of study entry * Patient dialyzes three times a week * Patient agrees to try ONS for the 6 month study period. * Patient has demonstrated an albumin \<3.5 g/dL on last available lab drawn in dialysis facility * Patient is adequately dialyzed with a Kt/V \> 1.4 at the most recent lab draw * Patient is capable of reading and comprehending Informed Consent Form and provides written informed consent

Exclusion criteria

* Peritoneal dialysis * Dysphagia * Aspiration risk * Difficulty swallowing * History of symptomatic intolerance to food or liquid consumption during dialysis treatments * Terminal illnesses with life expectancy \<6 months, e.g. stage IV cancer or full blown AIDS * Concurrent appetite stimulants * Use of IDPN in last 3 months * Inability to follow and to comply with the instructions and guidelines * Severe liver disease defined as most recent SGOT \> 78 * Active malignancy (other than skin) * Major surgery within previous 6 months or anticipated during the 90-day study period * Females who are pregnant or are breast-feeding * Considered clinically unstable by the treating nephrologists * Noncompliance with dialysis treatments ( Missed \> 2 treatments in prior month due to noncompliance) * Extended or frequent hospitalizations defined as hospitalization of longer than 15 days with discharge within the last 30 days or greater than 3 admissions within the last 30 days * Regular supplement use defined as consumption of \> 7 servings of a commercially available kcal/ protein supplement in the prior month * Any clinically significant medical disease or condition that, in the investigator's opinion, may interfere with protocol adherence or a patient's ability to give informed consent

Design outcomes

Primary

MeasureTime frame
The primary outcome measure of this study is albumin level, both mean albumin level and percentage of patients achieving an albumin level of >3.8 and > 4.0Monthly for the 6 month study period

Secondary

MeasureTime frame
Malnutrition Inflammation Score (MIS)Month 0 and Month 6
Body Mass Index (BMI)Monthly for the 6 month study period
Estimated Dry Weight (EDW)Monthy for the 6 monthly study period
Prealbumin levelMonths 0,2,4,&6
C-Reactive protein levelMonth 0,3 &6

Countries

United States

Outcome results

None listed

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