Oral Nutritional Supplement Intervention Among Hemodialysis Patients With Sarcopenic Obesity
Primary Purpose
Chronic Kidney Disease Requiring Chronic Dialysis, Sarcopenic Obesity, Body Composition
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
ReGen 18%
Sponsored by
About this trial
This is an interventional other trial for Chronic Kidney Disease Requiring Chronic Dialysis focused on measuring Oral nutritional supplement, Sarcopenic obesity, Body composition
Eligibility Criteria
Inclusion Criteria:
- Aged between 40 y/o and 90 y/o
- Regular hemodialysis treatment at least 3 months
- Hemodialysis treatment thrice a week, 3.5-4.5 hours/session
- Body composition: body mass index < 28 kg/m2 and body fat percentage >25% for males or >35% for females
- The normalized protein catabolic rate (nPCR) < 1.2 g/kg/day
Exclusion Criteria:
- Inadequate Kt/V <1.2
- Active malignancy
- Liver cirrhosis
- Active infection, including tuberculosis and AIDS
- Kidney transplant less than 6 months before study enrollment
- Patients hospitalized for more than 5 days within 3 months preceding enrollment
- Patients received intradialytic parental nutrition within 2 months preceding enrollment
- Inability to perform hand grip test, including patients with NG feeding or under bed-ridden status
- Patients with a cardiac pacemaker or metallic implants
- Patients are amputees
- Pregnant woman
- History of poor adherence to dialysis or medication
Sites / Locations
- Taipei Tzu Chi HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention
Control
Arm Description
The subjects will be assigned to receive nutritional supplement consisting of one can of ReGen 18% (19.1 g protein, 425 Kcal) daily and standard care.
The subjects will be assigned to receive standard care alone.
Outcomes
Primary Outcome Measures
Change in lean tissue mass in kg
Measured by bioimpedance device
Secondary Outcome Measures
Change in dry weight in kg
Measured by bioimpedance device
Change in body mass index in kg/m^2
Measured by bioimpedance device
Change in fat tissue mass in kg
Measured by bioimpedance device
Change in muscle strength in kg
Handgrip test
Change in albumin in mg/dl
laboratory test
Change in CRP in mg/L.
laboratory test
Full Information
NCT ID
NCT03347773
First Posted
November 12, 2017
Last Updated
November 15, 2017
Sponsor
Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
1. Study Identification
Unique Protocol Identification Number
NCT03347773
Brief Title
Oral Nutritional Supplement Intervention Among Hemodialysis Patients With Sarcopenic Obesity
Official Title
Oral Nutritional Supplement Intervention Among Hemodialysis Patients With Sarcopenic Obesity: a Pilot/Feasibility Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2017 (Actual)
Primary Completion Date
April 2018 (Anticipated)
Study Completion Date
April 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Chronic kidney disease patients with sarcopenic obesity are noted to have impairment in physical performance and reducing their quality of life, and the investigators also founded these patients are at higher risk of mortality. Thus, the investigators hypothesize that oral nutrition intervention could increase lean tissue mass in these patients and improve the clinical outcomes.
Detailed Description
In chronic kidney disease (CKD) patients, disease- and age- related changes in body composition, as well as the increased prevalence of obesity, determine a combination of excess weight and reduced muscle mass or strength, recently defined as sarcopenic obesity. The prevalence of sarcopenic obesity increase with lower eGFR, and previous studies showed that up to 18.3% stage 4 CKD patients and 56% prevalent hemodialysis patient to be with sarcopenic obesity. Sarcopenic obesity was negatively correlated with physical performance and quality of life. In the investigator's previous study, nondialysis-dependent CKD patients with normal body mass index (BMI) but excess body fat had the highest risk of death compared to those with BMI above the cutoff for obesity and excess body fat during a follow up of 5 years. These patients with excess body fat but lower lean tissue mass was what so called "sarcopenic obesity" group.
Hemodialysis therapy per se has been shown to be a catabolic process. Pupim et al. showed that in eight malnourished patients undergoing hemodialysis, highly positive whole-body net protein balance during hemodialysis and improvement of skeletal muscle protein homeostasis was achieved with an intradialytic oral nutritional supplement (ONS) compared to the control, and ONS during hemodialysis resulted in persistent anabolic benefits for muscle protein metabolism in the posthemodialysis phase. In the past, randomized trials of nutritional supplement intervention in dialysis patients were focused on populations with protein energy wasting, and most studies used change in serum albumin concentration as the surrogate marker. Studies focused on dialysis patients with sarcopenic obesity are sparse. Therefore, the investigators hypothesize that ONS could improve the nutritional status among dialysis patients with sarcopenic obesity, especially increase in lean tissue, and improve clinical outcomes. This pilot/feasibility study is aimed to conduct a randomised controlled pilot trial of the feasibility of undertaking a study to assess the effect of ONS on the nutritional status of haemodialysis patients with sarcopenic obesity and will lead to a more robust definitive trial in the future.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease Requiring Chronic Dialysis, Sarcopenic Obesity, Body Composition
Keywords
Oral nutritional supplement, Sarcopenic obesity, Body composition
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Open label randomized controlled trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
The subjects will be assigned to receive nutritional supplement consisting of one can of ReGen 18% (19.1 g protein, 425 Kcal) daily and standard care.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The subjects will be assigned to receive standard care alone.
Intervention Type
Dietary Supplement
Intervention Name(s)
ReGen 18%
Intervention Description
ReGen 18% is a kind of oral nutritional supplement, designed for patients under regular hemodialysis. One can of ReGen 18% contains 237ml, 425 Kcal, 19.1g protein, 22.7g lipid and 37.9g carbohydrate.
Primary Outcome Measure Information:
Title
Change in lean tissue mass in kg
Description
Measured by bioimpedance device
Time Frame
Measured at baseline and end of study, 4 months apart
Secondary Outcome Measure Information:
Title
Change in dry weight in kg
Description
Measured by bioimpedance device
Time Frame
Measured at baseline and end of study, 4 months apart
Title
Change in body mass index in kg/m^2
Description
Measured by bioimpedance device
Time Frame
Measured at baseline and end of study, 4 months apart
Title
Change in fat tissue mass in kg
Description
Measured by bioimpedance device
Time Frame
Measured at baseline and end of study, 4 months apart
Title
Change in muscle strength in kg
Description
Handgrip test
Time Frame
Measured at baseline and end of study, 4 months apart
Title
Change in albumin in mg/dl
Description
laboratory test
Time Frame
Measured at baseline and end of study, 4 months apart
Title
Change in CRP in mg/L.
Description
laboratory test
Time Frame
Measured at baseline and end of study, 4 months apart
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged between 40 y/o and 90 y/o
Regular hemodialysis treatment at least 3 months
Hemodialysis treatment thrice a week, 3.5-4.5 hours/session
Body composition: body mass index < 28 kg/m2 and body fat percentage >25% for males or >35% for females
The normalized protein catabolic rate (nPCR) < 1.2 g/kg/day
Exclusion Criteria:
Inadequate Kt/V <1.2
Active malignancy
Liver cirrhosis
Active infection, including tuberculosis and AIDS
Kidney transplant less than 6 months before study enrollment
Patients hospitalized for more than 5 days within 3 months preceding enrollment
Patients received intradialytic parental nutrition within 2 months preceding enrollment
Inability to perform hand grip test, including patients with NG feeding or under bed-ridden status
Patients with a cardiac pacemaker or metallic implants
Patients are amputees
Pregnant woman
History of poor adherence to dialysis or medication
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ting-Yun Lin, MD
Phone
8862-6628-9779
Ext
2350
Email
water_h2o_6@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Szu-Chun Hung, MD
Phone
8862-6628-9779
Ext
2350
Email
szuchun.hung@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ting-Yun Lin, MD
Organizational Affiliation
Taipei Tzu Chi Hospital, Division of Nephrology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Taipei Tzu Chi Hospital
City
New Taipei City
ZIP/Postal Code
231
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ting-Yun Lin, MD
Phone
8862-6628-9779
Ext
2350
Email
water_h2o_6@hotmail.com
First Name & Middle Initial & Last Name & Degree
Szu-chun Hung, MD
Phone
8862-6628-9779
Ext
2350
Email
szuchun.hung@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
25392147
Citation
Sharma D, Hawkins M, Abramowitz MK. Association of sarcopenia with eGFR and misclassification of obesity in adults with CKD in the United States. Clin J Am Soc Nephrol. 2014 Dec 5;9(12):2079-88. doi: 10.2215/CJN.02140214. Epub 2014 Nov 12.
Results Reference
background
PubMed Identifier
24179011
Citation
Gracia-Iguacel C, Qureshi AR, Avesani CM, Heimburger O, Huang X, Lindholm B, Barany P, Ortiz A, Stenvinkel P, Carrero JJ. Subclinical versus overt obesity in dialysis patients: more than meets the eye. Nephrol Dial Transplant. 2013 Nov;28 Suppl 4:iv175-81. doi: 10.1093/ndt/gft024.
Results Reference
background
PubMed Identifier
24763868
Citation
Martinson M, Ikizler TA, Morrell G, Wei G, Almeida N, Marcus RL, Filipowicz R, Greene TH, Beddhu S. Associations of body size and body composition with functional ability and quality of life in hemodialysis patients. Clin J Am Soc Nephrol. 2014 Jun 6;9(6):1082-90. doi: 10.2215/CJN.09200913. Epub 2014 Apr 24.
Results Reference
background
PubMed Identifier
17021267
Citation
Pupim LB, Majchrzak KM, Flakoll PJ, Ikizler TA. Intradialytic oral nutrition improves protein homeostasis in chronic hemodialysis patients with deranged nutritional status. J Am Soc Nephrol. 2006 Nov;17(11):3149-57. doi: 10.1681/ASN.2006040413. Epub 2006 Oct 4.
Results Reference
background
PubMed Identifier
21629229
Citation
Kalantar-Zadeh K, Cano NJ, Budde K, Chazot C, Kovesdy CP, Mak RH, Mehrotra R, Raj DS, Sehgal AR, Stenvinkel P, Ikizler TA. Diets and enteral supplements for improving outcomes in chronic kidney disease. Nat Rev Nephrol. 2011 May 31;7(7):369-84. doi: 10.1038/nrneph.2011.60.
Results Reference
background
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Oral Nutritional Supplement Intervention Among Hemodialysis Patients With Sarcopenic Obesity
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