Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Deka Research and Development
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Completed DEKA Protocol DKPL 00057 001 and are qualified to enter the study based on the assessment of the Investigator.
Are willing to comply and capable of complying with the study requirements for therapy with the HemoCare™ Hemodialysis System.
Have a trained study care partner able to support subject for all at-home study treatments.
Subject and care partner can read and understand English and provide written informed consent.
Have a stable functioning vascular access as judged by the treating physician.
You may not be if
Have a current self-reported pregnancy or are actively planning to become pregnant within the next 12 months, lactating, or not using medically acceptable means of contraception during the study.
Have any any other clinically significant medical disease or condition or subject responsibility that, in the Investigator's opinion, may interfere with a subject's (and/or care partner's) ability to give informed consent, adhere to the protocol, interfere with assessment of the investigational product (IP), or serve as a contraindication to the subject's participation in the study.
Have a significant psychiatric disorder or mental disability that could interfere with the subject's ability to provide informed consent and/or comply with study procedures.
Are participating or planning to participate in any other interventional studies except DKPL-00057-001.
