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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01214447
Other study ID # 132/10
Secondary ID
Status Recruiting
Phase N/A
First received October 3, 2010
Last updated October 4, 2010
Start date October 2010
Est. completion date December 2013

Study information

Verified date September 2010
Source Assaf-Harofeh Medical Center
Contact Ilia Beberashvili, MD
Phone +97289779383
Email iliab@asaf.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 2013
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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)

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
No intervention
Observational study - no intervention

Locations

Country Name City State
Israel Assaf Harofeh Medical Center Zerifin

Sponsors (1)

Lead Sponsor Collaborator
Assaf-Harofeh Medical Center

Country where clinical trial is conducted

Israel, 

References & Publications (1)

Beberashvili I, Azar A, Sinuani I, Yasur H, Feldman L, Averbukh Z, Weissgarten J. Objective Score of Nutrition on Dialysis (OSND) as an alternative for the malnutrition-inflammation score in assessment of nutritional risk of haemodialysis patients. Nephrol Dial Transplant. 2010 Aug;25(8):2662-71. doi: 10.1093/ndt/gfq031. Epub 2010 Feb 26. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary All cause morbidity and mortality 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.
during 2 years of observation No
Secondary All cause morbidity and mortality Associations 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
2 years No