NCT01654926|Completed
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Sponsor study identifier
observational
38
1 country
1
Study Start
December 2012
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
September 2013
Actual (reported)Study Completion
October 2013
Actual (reported)Ultrafiltration (UF) technology is unique for its ability to extract fluid as an isotonic solution, therefore not causing substantial changes in NaCl concentrations, and the use of peripheral veins makes it feasible to use in out of hospital medical centers, for non compensated Heart Failure (HF) with a low response to diuretics. The use of UF in the United States and Europe in out of hospital HF centers is accepted as daily practice. Therefore the hypothesis of this study is that it is feasible for a professional team to effectively use the UF for short courses on non compensated HF patients with low or no response to Diuretics, in a dedicated out of hospital HF center.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
October 2013
Actual (reported)Click on a node to explore related trials.
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
July 29, 2012
Actual (reported)August 1, 2012
Actual (reported)December 2012
Date type not reportedThis date has not been verified as actual or estimated.
September 2013
Actual (reported)October 2013
Actual (reported)Feasibility Assessment of the Aquadex FlexFlowTM Ultrafiltration System in Treating Non-Hospitalized Heart Failure Patients in Dedicated Heart Failure Centers
The propose of the study is to observe the administrative needs of performing the treatment at our specific out-patient clinic. Of note the treatment is already approved including the indication and the place we are doing it so we merely aim to look at administrative and logistic that need to be done.
12 months
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
HF patients
Lin Clinic
Haifa, Israel
38 participants (actual enrollment reported by the registry).
First Submitted
July 29, 2012
First Posted
August 1, 2012
Study Start
December 2012
Date type not reportedThis date has not been verified as actual or estimated.
Contact the study team to confirm eligibility.
Primary Completion
September 2013
Actual (reported)Study Completion
October 2013
Actual (reported)Last Updated
March 10, 2015
Record last verified: 2015-03
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Source: ClinicalTrials.gov.
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