Tolerance to Hemodialysis in Insulin-Requiring Diabetic Patients: BD vs AFB With Blood Volume Biofeedback (THIRD)

This study has been completed.
Sponsor:
Information provided by:
Università degli Studi di Brescia
ClinicalTrials.gov Identifier:
NCT01098149
First received: March 29, 2010
Last updated: April 1, 2010
Last verified: March 2010

March 29, 2010
April 1, 2010
March 2006
March 2010   (final data collection date for primary outcome measure)
Investigate a possible better tolerance to dialysis, eliminating acetate in the dialysate bath, with AFB treatment, and using, at the same time, the automatic blood volume control (BVC). [ Time Frame: 3 months ] [ Designated as safety issue: No ]

The treatment tolerance is measured by the number of intradialytic hypotensive events, defined as:

  • systolic blood pressure less then 90 mmHg;
  • systolic blood pressure more then 25 mmHg to the predialysis value, with hypotensive events requiring therapies;
  • systolic blood pressure less then 90 mmHg with hypotensive events requiring therapies for those patients, which predialysis systolic blood pressure value was 100 mmHg.
Same as current
Complete list of historical versions of study NCT01098149 on ClinicalTrials.gov Archive Site
The secondary outcome measure is to evaluate the relative efficiency of each factor (AFB in the bath and blood volume control) to reach this result. [ Time Frame: 3 months ] [ Designated as safety issue: No ]

The evaluation will be done on:

  • frequency of hypotensive events, during dialysis (defined as above);
  • number of nurse interventions (defined as ultrafiltration rate stop, or saline infusion);
  • antihypertensive drugs.
Same as current
Not Provided
Not Provided
 
Tolerance to Hemodialysis in Insulin-Requiring Diabetic Patients: BD vs AFB With Blood Volume Biofeedback
Tolerance to Hemodialysis in Insulin-Requiring Diabetic Patients: a Prospective Randomized,Cross-over Multicenter Study Between Bicarbonate Dialysis (BD) and Blood Volume Controlled Acetate-Free Biofiltration (BVC-AFB)

Diabetic nephropathy is becoming the most common primary renal disease in end stage renal disease patients. The prevalence of diabetic patients in dialysis reaches even the 30% of the dialysis population (USRDS) with an incidence rate, in some countries, up to 40%. The 5 years surviving time of diabetic patients in dialysis is about the 20% and, compared to the hypertension and glomerulonephritis complications, still remains the worst. Diabetes is often associated to several comorbid factors such as hypertension, autonomic neuropathy, vasculopathy, metabolic disorders (ketoacidosis, poor glycaemic control), and electrolyte disorders. So, the diabetic patient is fragile, with a rather poor tolerance to dialysis, lack of achievement of dry body weight and inadequate dialysis. In order to gain a more detailed insight into a possible better tolerance to dialysis, arising from the elimination of acetate in dialysate bath (Acetate Free Biofiltration) and from the use of an automatic system to control the blood volume (Blood Volume Control),the investigators would like to investigate the cardiovascular stability and the frequency of intradialytic symptoms in a prospective, randomized, cross-over study.

Acetate-Free-Biofiltration (AFB) was proved to be a technique suitable to treat critical patients, such as elders and diabetics, because of frequency reduction of hypotensive episodes and symptoms during the treatment and a better control to metabolic aspects (such as metabolic acidosis).

The Blood Volume Control (BVC) is a tool, that allows to improve the cardiovascular tolerance to the treatment, especially in hypotension-prone patients, appearing promising in the correction of the arterial hypertension induced by the hydro-saline overload.

The use of BVC in AFB has been tested to verify the behaviour of the kinetics of electrolyte (in particular of bicarbonate) and it has got good results, in terms of a further improvement in treatment tolerance, for critical patients However, this therapy (AFB+BVC) was not yet evaluated as the dialysis tolerance improvement in diabetics concern, nor the relative contribution given by each factor in achieving this result.

The study, 9 months long, is aimed to verify the treatment tolerance of insulin requiring diabetic patients, by using standard bicarbonate dialysis (BD), or Acetate Free Biofiltration (AFB) and/or a Blood Volume Control(BVC). The study is divided in three phases: the first one, three months long, is the baseline in standard bicarbonate dialysis, then all the patients are shifted to AFB with BVC, for other three months, while the last three months long phase, after a randomization, has the aim to identify the relative contribution of each factor (absence of acetate in the bath or BVC) in the treatment tolerance improvement(if any). The treatment tolerance will be evaluated considering the frequency of intradialytic hypotensive events.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Hypotension
  • Hemodialysis
Other: BD and BVC, AFB
Some patients are randomized into the AFB, the others into the BD and BVC
Other Name: Biofeedback,Blood Volume Control,Acetate Free Biofiltration
  • Active Comparator: AFB stand alone
    Patients are switched in AFB treatment, without blood volume control.
    Intervention: Other: BD and BVC, AFB
  • Active Comparator: BD and BVC
    Patients are switched into bicarbonate dialysis with Blood Volume Control
    Intervention: Other: BD and BVC, AFB

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
55
March 2010
March 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • End stage renal disease patients
  • Patients affected by diabetic nephropathy with insulin therapy, for, at least, 6 months
  • Patients with renal replacement therapy with haemodialysis three time a week, for, at least, 6 months.
  • Age between 18 and 85 years

Exclusion Criteria:

  • Patients affected by neoplasm and/or mental illness
  • Patients with residual diuresis > 500 ml/die;
  • Patients in single needle bicarbonate dialysis.
Both
18 Years to 85 Years
No
Contact information is only displayed when the study is recruiting subjects
Italy
 
NCT01098149
THIRD-01
Yes
Dott.Ezio Movilli, Dept of Nephrology -Brescia
Università degli Studi di Brescia
Not Provided
Study Chair: Giovanni Cancarini, MD Università of Brescia
Università degli Studi di Brescia
March 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP