DaVita Assessment of Nutritional Supplement Effects (DANSE)

This study has been completed.
Sponsor:
Collaborator:
Abbott Nutrition
Information provided by:
Davita Clinical Research
ClinicalTrials.gov Identifier:
NCT00895401
First received: May 7, 2009
Last updated: February 5, 2011
Last verified: February 2011

May 7, 2009
February 5, 2011
April 2009
January 2011   (final data collection date for primary outcome measure)
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 > 4.0 [ Time Frame: Monthly for the 6 month study period ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00895401 on ClinicalTrials.gov Archive Site
  • Malnutrition Inflammation Score (MIS) [ Time Frame: Month 0 and Month 6 ] [ Designated as safety issue: No ]
  • Body Mass Index (BMI) [ Time Frame: Monthly for the 6 month study period ] [ Designated as safety issue: No ]
  • Estimated Dry Weight (EDW) [ Time Frame: Monthy for the 6 monthly study period ] [ Designated as safety issue: No ]
  • Prealbumin level [ Time Frame: Months 0,2,4,&6 ] [ Designated as safety issue: No ]
  • C-Reactive protein level [ Time Frame: Month 0,3 &6 ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
DaVita Assessment of Nutritional Supplement Effects (DANSE)
DaVita Assessment of Nutritional Supplement Effects

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.

Not Provided
Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Malnutrition
  • Dietary Supplement: Nepro 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.
    Other Name: Oral Nutritional Supplement
  • Other: Standard of Care
    Standard of Care for malnourished maintenance hemodialysis patients
  • Active Comparator: Standard of Care
    Standard of Care for malnourished maintenance hemodialysis patients
    Intervention: Other: Standard of Care
  • Experimental: Nepro with Carb Steady
    Nepro with Carb Steady is a commercially available nutritional supplement designed to meet the nutritional needs of malnourished hemodialysis patients. The serving size is 8 oz which provides 425 kcal and 19 g protein
    Intervention: Dietary Supplement: Nepro with Carb Steady
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
160
Not Provided
January 2011   (final data collection date for primary outcome measure)

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
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00895401
2009-001
Yes
Debbie Benner, MA, RD, CSE, DaVita, Inc
Davita Clinical Research
Abbott Nutrition
Principal Investigator: Debbie Benner, MA DaVita Dialysis
Davita Clinical Research
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP