Status:
TERMINATED
Evaluation of Daily HemoDialysis at Low Dialysate Flow in Patients Previously Treated With Conventional Hemodialysis
Lead Sponsor:
Association Pour L'utilisation Rein Artificiel Région Lyonnaise
Collaborating Sponsors:
Association Nationale pour la promotion de la Dialyse Quotidienne (ANDIQ, France)
Conditions:
End Stage Renal Disease
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
HDQ 200 is an interventional multicenter study. This is a before-and-after design in which the patient is his own control. The main objective of the study is to determine the percentage of success of ...
Eligibility Criteria
Inclusion
- Age ≥ 18 years
- Patients who give voluntary signed informed consent
- Patients affiliated with the French universal health care system or similar
- For women of childbearing potential: serum or urine negative pregnancy test
- Patients treated with conventional hemodialysis (3 times 4h to 5h per week at at least a dialysate flow rate of 500 ml/min) for at least 3 months and clinically stable (investigator assessment)
- Bipuncture patients (or with double lumen central venous catheter) with stable vascular access and easy to puncture
- Patients willing to be treated with daily hemodialysis at low dialysate flow during the study period (6 times 2h to 2h30 per week at a dialysate flow rate of 200 ml/min in order that the total duration of weekly dialysis is equivalent to the duration of weekly dialysis during the last 3 months of conventional hemodialysis)
Exclusion
- Pregnant women or women who could become pregnant during the study (planned pregnancy within 3 months)
- Patients not affiliated with the French universal health care system
- Minor patients
- Patients who are protected adults according to the terms of the law (French public health laws).
- Refusal to give consent
- Patients simultaneously participating in another trial that may interfere with the study results
Key Trial Info
Start Date :
July 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2015
Estimated Enrollment :
2 Patients enrolled
Trial Details
Trial ID
NCT01845012
Start Date
July 1 2012
End Date
January 1 2015
Last Update
March 17 2017
Active Locations (13)
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1
Cliniques universitaires St Luc
Brussels, Belgium, 1200
2
ECHO Angers
Angers, France, 49055
3
CTMR Saint Augustin
Bordeaux, France, 33000
4
CHPC
Cherbourg, France, 50102