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Validity and Reproducibility of OSND (Objective Score of Nutrition on Dialysis) as a Nutritional Marker in End-stage Renal Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01214447
Enrollment
300
Registered
2010-10-05
Start date
2010-10-31
Completion date
2013-12-31
Last updated
2010-10-05

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

Conditions

Hemodialysis Nutritional Risk Stratification, Malnutrition-Inflammation Syndrome

Keywords

Hemodialysis, Inflammation, Malnutrition, Phase Angle

Brief summary

This prospective observational study is planned to validate OSND against the prospective morbidity and mortality in chronic hemodialysis patients and to examine the hypothesis that OSND risk stratification of chronic HD patients is useful in predicting outcomes and better than its component alone or in diverse combinations. The investigators specific aim is to validate OSND in chronic HD patients by comparing it with conventional measures of nutritional state, including blood tests, anthropometry, MIS, GNRI, bioelectric impedance analysis and several measures of clinical outcome including prospective mortality and hospitalization.

Interventions

OTHERNo intervention

Observational study - no intervention

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female, age \> 18 years, in chronic hemodialysis treatment at least 3 months 2. Stable and adequate hemodialysis treatment three months prior to participation in study as defined by Kt/V \> 1.2 and/or hemodialysis performed 4 hours 3 times weekly 3. Patients with normal hydration status (edema-free), with no neuroid-muscular diseases 4. Informed consent obtained before any trial-related activities

Exclusion criteria

1. Patients with edema, pleural effusion or ascites at their initial assessment 2. Patients with active malignant disease or liver cirrhosis 3. Patients with neuroid-muscular diseases 4. Patients on chronic treatment with steroids on doses \> 10 mg/day Prednisone (or equivalent) 5. Patients treated with immunosuppressive agents 6. Patients suffering from * Acute vasculitis * Severe systemic infections * Heart failure (NYHA class III-IV)

Design outcomes

Primary

MeasureTime frameDescription
All cause morbidity and mortalityduring 2 years of observation* Associations of OSND with: * Morbidity: Days at hospital (over night stay). Measured from baseline to end of study * Morbidity: Number of sick days during the study period * Morbidity: Number of visits to health care professionals other than hospitals * Mortality: From baseline visit to end of study * Interobserver reproducibility of OSND.

Secondary

MeasureTime frameDescription
All cause morbidity and mortality2 yearsAssociations of MIS, GNRI and phase angle with: * Morbidity: Days at hospital (over night stay). Measured from baseline to end of study * Morbidity: Number of sick days during the study period * Morbidity: Number of visits to health care professionals other than hospitals * Mortality: From baseline visit to end of study

Countries

Israel

Contacts

Primary ContactIlia Beberashvili, MD
iliab@asaf.health.gov.il+97289779383

Outcome results

None listed

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