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NCT Number: NCT00413803

Comparison of Four and Eight Hours Dialysis Sessions in Thrice Weekly Hemodialysis

The investigators hypothesize that an increase in the duration of dialysis session in thrice weekly center hemodialysis may provide better outcome, less morbidity, higher quality of life, lesser requirement of medications, and lower total cost.

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Key information

About this study

The proposed prospective and controlled clinical trial aims to compare 4-hour and 8-hour dialysis sessions in thrice weekly center HD regarding mortality, hospitalization rate, several clinical and laboratory parameters, and total cost. Four hundred and ten HD patients will be taken into the study. The study will last for 12 months. The patients will be placed in two groups:

  • Four-hour dialysis session, blood flow rate 300-400 ml/min
  • Eight-hours dialysis session, blood flow rate 200-250 ml/min

Sample size is estimated with following hypotheses: twelve months duration of follow-up; twelve months survival of the control group 85%; a bilateral alpha risk equal to 5%; an expectation that 12-months survival to be 95% by 8-hours dialysis; a 85% power to detect the decrease in annual mortality by 8-hours dialysis comparing to 4-hours dialysis; a 10% of dropout rate. The required sample is total 410 patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Older than 18-years
  • On maintenance bicarbonate HD scheduled thrice weekly 12 hours/week; achieved mean single pool Kt/V above 1.2
  • Willingness to participate in the study with a written informed consent

Exclusion criteria

  • To be scheduled for living donor renal transplantation
  • To have serious life-limiting co-morbid situations, namely active malignancy, active infection, end-stage cardiac, pulmonary, or hepatic disease
  • Pregnancy or lactating
  • Current requirement for HD more than three times per week due to medical comorbidity
  • GFR greater than 10 ml/min/1.73 m2 as measured by the average of urea and creatinine clearances obtained from a urine collection of at least 24 hours
  • Use of temporary catheter
  • Current use of investigational drugs or participation in an interventional clinical trial that contradicts or interferes with the therapies or measured outcomes in this trial
  • Mental incompetence

Treatment and study plan

4-hour thrice weekly in center hemodialysis

Procedure

conventional hemodialysis

8-hour thrice weekly in center hemodialysis

Procedure

long dialysis

Primary outcomes

  1. total mortality

    Time frame: one year

Secondary outcomes

  1. cardiovascular mortality

    Time frame: one year

  2. changes in health-related quality of life, depression burden, cognitive function

    Time frame: one year

  3. required medications

    Time frame: one year

  4. total cost

    Time frame: one year

  5. changes in blood pressure, left ventricular geometry, coronary artery calcification, arterial stiffness,upper mid-arm circumference,hematocrit and related rHu-EPO doses, the levels of phosphorus, albumin, lipid parameters, hsCRP, and β-2 microglobulin

    Time frame: one year

  6. hospitalization rate

    Time frame: one year

  7. Vascular access patency

    Time frame: one year

  8. post-dialysis body weight and total body water

    Time frame: one year

  9. arrythmia episodes determined by Holter-ECG

    Time frame: one year

Sponsors and collaborators

Lead sponsor

Ege University

Other

Collaborators

  • Fresenius Medical Care North America

Registry information

Official study title

Comparison of Four and Eight Hours Dialysis Sessions in Thrice Weekly Hemodialysis: Long Dialysis Study

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Dec 20, 2006
Registry last updated
Aug 4, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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