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HFR A-equilibrium on Cardiovascular Stability (AIMS)

Primary Purpose

Hypotension

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Automated sodium profiling in endogenous hemodiafiltration
Standard sodium dialysate
Sponsored by
Azienda Ospedaliera di Lecco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypotension

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with more than 30% of dialysis complicated by hypotension
  • age between 18 and 85 yers
  • time on dialysis greater than 6 months
  • residual creatinine clearance less than 2 ml/min/1.73 m2
  • native fistula or central venous catheter with blood flow rate greater than 250 ml/min

Exclusion Criteria:

  • Life expectancy less than 1 year
  • solid active neoplasm
  • pregnancy
  • major event in the previous 3 months (ictus, myocardial infarction, cachexia)

Sites / Locations

  • Hospital Erasme
  • Dept. of Nephrology and Dialysis Centre Pasteur Vallery Radat
  • Civil Hospital Bretagne Atlantique
  • Clinic of Internal Medicine
  • Nephrology and Dialysis Unit Ospedali Riuniti
  • UO Nefrologia Dialisi e Trapianto Policlinico S. Orsola Malpighi
  • Civil Hospital
  • PO Lastaria
  • Hospital Maggiore della Carità
  • Casa Sollievo della Sofferenza
  • Ospedale San Giovanni Bosco
  • Hospital Val d'Hebron

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard

Automated profiled

Arm Description

Standard constant (no profiled) sodium dialysate used during endogenous hemodiafiltration

Automate sodium profiling in endogenous hemodiafiltration

Outcomes

Primary Outcome Measures

Number of dialysis complicated by at least one hypotension
Hypotension definition: If predialysis systolic blood pressure greater than100 mmHg then a value during dialysis below 90 mmHg or any systolic blood pressure reduction greater than 25 mmHg in presence of symptoms or If predialysis systolic blood pressure less than 90 mmHg a reduction of at least 10% accompanied by symptoms

Secondary Outcome Measures

Blood Pressure Intradialytic symptoms
Systolic, diastolic blood pressures (SBP, DBP) and heart rate (HR) measured at the beginning of each treatment and every 30 minutes till the end of dialysis; intradialytic symptoms (nausea, vomiting, hypotension, headache, cramps) and related clinical interventions.

Full Information

First Posted
August 10, 2011
Last Updated
August 26, 2011
Sponsor
Azienda Ospedaliera di Lecco
Collaborators
IRCCS Azienda Ospedaliero-Universitaria di Bologna, Centre Pasteur Vallery Radot
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1. Study Identification

Unique Protocol Identification Number
NCT01414842
Brief Title
HFR A-equilibrium on Cardiovascular Stability
Acronym
AIMS
Official Title
Randomized Controlled Study on the Effect of the Hemodiafiltration Plasma Sodium Biofeedback System on Cardiovascular Stability in Hemodialysis Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2007
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliera di Lecco
Collaborators
IRCCS Azienda Ospedaliero-Universitaria di Bologna, Centre Pasteur Vallery Radot

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Aim of the present randomized controlled multinational trial is the comparison of a novel biofeedback system on sodium profiling applied to a endogenous hemodiafiltration therapy, with the standard (no sodium profiling) hemodiafiltration technique on the intradialytic overall and cardiovascular stability.
Detailed Description
Online hemodiafiltration (OL-HDF) has been recently associated with better patient survival in comparison with standard hemodialysis in some large observational studies (Canaud et al, KI, 2006; Vilar et al, CJASN , 2009) supporting the hypothesis that convection can improve patients outcomes. Moreover, it has been demonstrated in randomized controlled trials (Locatelli et al, Journal American Society of Nephrology, 2010) that OL-HDF significantly reduced the frequency of intradialytic hypotension. Nonetheless, the associated comorbidities and ageing of dialysis population require further devices able to improve treatment tolerance. Among these tools, the sodium profiling and biofeedback system seem to be promising to accomplish this task. But the correct intradialytic sodium balance is still far away today to be easily achieved. The use of an automated adaptive system dialysis to the sodium profiling has been investigated in a feasibility trial (Colì et al International Journal Artificial Organs, 2003). They also investigated the impact of such a device on treatment tolerance. The aim of this randomized multinational multicenter controlled trial is to evaluate the impact of sodium profiling applied to a endogenous hemodiafiltration technique on the intradialytic cardiovascular stability in comparison to standard no profiled endogenous hemodiafiltration.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypotension

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard
Arm Type
Active Comparator
Arm Description
Standard constant (no profiled) sodium dialysate used during endogenous hemodiafiltration
Arm Title
Automated profiled
Arm Type
Experimental
Arm Description
Automate sodium profiling in endogenous hemodiafiltration
Intervention Type
Device
Intervention Name(s)
Automated sodium profiling in endogenous hemodiafiltration
Other Intervention Name(s)
HFR-Aequilibrium
Intervention Description
Automated sodium profiling during endogenous reinfusion hemodiafiltration technique. The device processes the dialysate sodium and ultrafiltration rate during dialysis to achieve a preset sodium target at the end of the treatment. Sodium dialysate and maximal ultrafiltration rate are constraint within safety limits during dialysis.
Intervention Type
Device
Intervention Name(s)
Standard sodium dialysate
Other Intervention Name(s)
Standard HFR
Intervention Description
Standard constant (no profiled) sodium dialysate used during endogenous hemodiafiltration
Primary Outcome Measure Information:
Title
Number of dialysis complicated by at least one hypotension
Description
Hypotension definition: If predialysis systolic blood pressure greater than100 mmHg then a value during dialysis below 90 mmHg or any systolic blood pressure reduction greater than 25 mmHg in presence of symptoms or If predialysis systolic blood pressure less than 90 mmHg a reduction of at least 10% accompanied by symptoms
Time Frame
six months
Secondary Outcome Measure Information:
Title
Blood Pressure Intradialytic symptoms
Description
Systolic, diastolic blood pressures (SBP, DBP) and heart rate (HR) measured at the beginning of each treatment and every 30 minutes till the end of dialysis; intradialytic symptoms (nausea, vomiting, hypotension, headache, cramps) and related clinical interventions.
Time Frame
six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with more than 30% of dialysis complicated by hypotension age between 18 and 85 yers time on dialysis greater than 6 months residual creatinine clearance less than 2 ml/min/1.73 m2 native fistula or central venous catheter with blood flow rate greater than 250 ml/min Exclusion Criteria: Life expectancy less than 1 year solid active neoplasm pregnancy major event in the previous 3 months (ictus, myocardial infarction, cachexia)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesco Locatelli, Prof.
Organizational Affiliation
Azienda Ospedaliera di Lecco
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital Erasme
City
Bruxelles
Country
Belgium
Facility Name
Dept. of Nephrology and Dialysis Centre Pasteur Vallery Radat
City
Paris
Country
France
Facility Name
Civil Hospital Bretagne Atlantique
City
Vannes
Country
France
Facility Name
Clinic of Internal Medicine
City
Rostock
Country
Germany
Facility Name
Nephrology and Dialysis Unit Ospedali Riuniti
City
Ancona
Country
Italy
Facility Name
UO Nefrologia Dialisi e Trapianto Policlinico S. Orsola Malpighi
City
Bologna
ZIP/Postal Code
40128
Country
Italy
Facility Name
Civil Hospital
City
Ciriè
Country
Italy
Facility Name
PO Lastaria
City
Foggia
Country
Italy
Facility Name
Hospital Maggiore della Carità
City
Novara
Country
Italy
Facility Name
Casa Sollievo della Sofferenza
City
San Giovanni Rotondo
Country
Italy
Facility Name
Ospedale San Giovanni Bosco
City
Torino
Country
Italy
Facility Name
Hospital Val d'Hebron
City
Barcellona
Country
Spain

12. IPD Sharing Statement

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HFR A-equilibrium on Cardiovascular Stability

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