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Effect of Oral Nutritional Supplementation on Oxidative Stress in Protein-energy Wasting Patients With Peritoneal Dialysis

H

Hospital Civil Juan I. Menchaca

Status

Unknown

Conditions

Oral Nutritional Supplements
Protein-Energy Wasting
Malnutrition
Peritoneal Dialysis
Oxidative Stress
Protein-Energy Malnutrition

Treatments

Dietary Supplement: Oral nutritional supplementation for kidney disease

Study type

Interventional

Funder types

Other

Identifiers

NCT04628117
HospitalCJIM

Details and patient eligibility

About

End-stage kidney disease (ESKD) represents a serious public health problem in Mexico. Data from the United States Renal Data System (USRDS) have reported that the region of Jalisco (Mexico) is one of the places with the highest incidence rate of treated ESKD and use of peritoneal dialysis (PD). In patients with ESKD, oxidative stress (OS) has been recognized as a potential source of morbidity and mortality, since it is involved in the pathogenesis of atherosclerosis and other complications of ESRD. This can induce damage to DNA (nucleic acid), proteins, carbohydrates, and lipids.

Another common complication in ESKD patients receiving PD is protein-energy wasting (PEW), which is characterized by the decline in the body stores of protein and energy fuels (that is, body protein and fat masses) due to the multiple nutritional and catabolic alterations that occur in this condition. Diverse factors can affect the nutritional and metabolic status of patients with PD, for which they require interventions to reverse protein and energy depletion. Nutritional counseling can be a useful tool in PD patients in order to improve compliance with nutritional recommendations. The strategies more used for PEW include oral nutritional supplementation. Therefore, the purpose of this study is assess the effect of oral nutritional supplementation on OS in PEW patients with PD.

Full description

The detection of patients is carried out in the Nephrology Service of the Hospital Civil de Guadalajara Dr. Juan I. Menchaca where the selection and exclusion criteria are evaluated.

The probabilistic group assignment is carried out using a sealed and opaque envelope.

Control group: only nutritional counselling for 8 weeks. Intervention group: nutritional counselling plus 237 mls per day of oral nutritional supplement for kidney disease.

Initial evaluation includes, anthropometric parameters and dietary intake. Demographic characteristics and OS levels, such as oxidants, antioxidants and oxidative DNA damage.

All nutritional counselling, dietary intake, medical nutrition theraphy (oral nutritional supplementation), assessment of OS levels, and anthropometric parameters will perform at 0, 4 and 8 weeks of follow up. Protein-energy wasting assessment only in the 0 and 8 weeks.

Enrollment

22 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of protein-energy wasting evaluated by 7-point Subjective Global Assessment (moderate/severe), and Malnutrition-inflammation Score (a score ≥ 6).
  • Male and female patients
  • Age ≥ 18 and <60 years
  • Receive continuous ambulatory peritoneal dialysis with at least 3 months of initiation of renal replacement therapy
  • Patients without clinical or biochemical evidence of any infectious process (peritonitis, urosepsis, endocarditis, soft tissue infection, pneumonia, etc) or inflammatory systemic disease (systemic lupus erythematosus, vasculitis, connective tissue disease)
  • Written informed consent

Exclusion criteria

  • Supplementation with exogenous antioxidants 2 months prior
  • Smoking less than 1 year
  • Intermittent peritoneal dialysis or automated peritoneal dialysis
  • PD catheter dysfunction
  • Known allergy or intolerance to oral nutritional supplement for renal disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

22 participants in 2 patient groups

Control
No Intervention group
Description:
Nutritional counselling by individualized nutritional plan for 8 weeks.
Oral nutritional supplementation
Experimental group
Description:
Nutritional counselling by individualized nutritional plan plus oral nutritional supplementation for renal disease (237 mls per day) for 8 weeks.
Treatment:
Dietary Supplement: Oral nutritional supplementation for kidney disease

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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