Metabolic and Inflammatory Responses to Hemodialysis and the Effect of a Meal

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
University of Aarhus
ClinicalTrials.gov Identifier:
NCT01446302
First received: September 29, 2011
Last updated: August 13, 2012
Last verified: August 2012

September 29, 2011
August 13, 2012
October 2011
May 2012   (final data collection date for primary outcome measure)
  • Changes in serum Bioactive IGF-I and IGFBP-1 levels during and after hemodialysis [ Time Frame: At 1, 2, 3, 5, 6, 7, 9, and 10 hours after start of hemodialysis ] [ Designated as safety issue: No ]
  • Changes in plasma Interleukin-6 and serum hsCRP levels during and after hemodialysis [ Time Frame: At 1, 2, 3, 5, 6, 7, 9, and 10 hours after start of hemodialysis ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01446302 on ClinicalTrials.gov Archive Site
  • Pulse wave analysis (augmentation index (AIx)) during and after hemodialysis [ Time Frame: At 1, 2, 3, ,4, 5, 6, 7, 8, 9, and 10 hours after start of hemodialysis ] [ Designated as safety issue: No ]
  • Mineral metabolism (including calcium, phosphate, PTH, and FGF-23 levels) during and after hemodialysis [ Time Frame: At 1, 2, 3, 5, 6, 7, 9, and 10 hours after start of hemodialysis ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Metabolic and Inflammatory Responses to Hemodialysis and the Effect of a Meal
Metabolic and Inflammatory Responses to Hemodialysis and the Effect of a Meal

The objective of this study is to characterize the hormonal and inflammatory responses to hemodialysis, and to determine the effect of a meal versus fast on the metabolic changes in the post-dialytic phase.

Studies show that hemodialysis (HD) is a protein catabolic event per se and probably contributes to the high prevalence of protein-energy wasting among HD patients. The muscle catabolic effect of HD is probably caused by loss of amino acids (10-12 grams per dialysis session) and by exacerbation of the inflammatory and hormonal disorders already present. Activation of the immune system during HD has been linked to the contact of blood cells with the dialyzer membrane and to bacterial-derived DNA fragments in the dialysis fluid. An intradialytic increase in interleukin-6 (IL-6) has been shown to correlate with muscle protein catabolism, and because IL-6 continues to increase for 2 hours after HD has ended, there might be a considerable "carry-over effect" to the post-dialytic period. Moreover, HD induces significant changes in the insulin/insulin-like growth factor I (IGF-I) signaling pathways. Plasma insulin is cleared by HD, and the bioactivity of IGF-I is reduced by 50% during a 4-hr maintenance HD due to an up-regulation of IGF-binding protein 1 (IGFBP-1), the only acutely regulated IGFBP.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Basic Science
Kidney Failure, Chronic
Dietary Supplement: Double meal
A standardized meal is served 1 h after start of HD and 1 h after end of HD.
  • Active Comparator: Double meal on a HD day
    A standardized meal is served 1 h after start of HD and 1 h after end of HD
    Intervention: Dietary Supplement: Double meal
  • No Intervention: Single meal on a HD day
    A standardized meal is served 1 h after start of HD. After the meal participants fast for 9 h (6 h after end of HD).
  • No Intervention: Single meal on a non-HD day
    A standardized meal is served 1 h after study start. After the meal participants fast for 9 h.
  • No Intervention: Single meal (healthy controls)
    A standardized meal is served 1 h after study start. After the meal participants fast for 9 h.
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
24
May 2012
May 2012   (final data collection date for primary outcome measure)

Inclusion criteria:

  • > 18 years
  • stable maintenance hemodialysis for at least 3 months
  • well-functioning arteriovenous shunts with recirculation less than 5%
  • informed consent

Exclusion criteria:

  • diabetes mellitus
  • body mass index below 18.5 or above 30.0 kg/m2
  • malnutrition (global assessment score C)
  • active malignant disease
  • immunosuppressive treatment (including glucocorticoid treatment)
  • evidence of an ongoing inflammatory disease (including infection and autoimmune disorders)
  • pregnancy

Exclusion criteria during the study:

  • myocardial infarction or arrythmia with hemodynamic derangements
  • permanent thrombosis in the arteriovenous (AV) shunt
  • severe infectious disease
  • renal transplantation
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT01446302
IGFHD2-2011
No
University of Aarhus
University of Aarhus
Not Provided
Study Director: Per Ivarsen, MD, PhD Department of Nephrology, Aarhus University Hospital, Skejby, Denmark
Study Director: Jan Frystyk, MD,PhD,DMSc Department of Endocrinology and Internal Medicine & Medical Research Laboratories, Clinical Institute, Aarhus University Hospital, Denmark
Study Director: Bente Jespersen, MD, DMSc Department of Nephrology, Aarhus University Hospital, Skejby, Denmark
Study Director: Jens S Christiansen, MD, DMSc Department of Endocrinology and Internal Medicine & Medical Research Laboratories, Clinical Institute, Aarhus University Hospital, Denmark
Study Director: Else Randers, MD, PhD Department of Nephrology, Viborg Regional Hospital, Denmark
Principal Investigator: Mark Reinhard, MD Department of Nephrology, Aarhus University Hospital, Skejby, Denmark
University of Aarhus
August 2012

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