A multi-institutional retrospective observational study on the clinical safety and efficacy of Central Dialysis fluid Delivery System (CDDS)

A multi-institutional retrospective observational study on the clinical safety and efficacy of Central Dialysis fluid Delivery System (CDDS) - A study on the clinical safety and efficacy of CDDS

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000040141

Enrollment

120

Registered

2020-06-01

Start date

2020-06-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic renal failure

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Chronic hemodialysis patients who receive maintenance hemodialysis at a frequency of 3 times / week at the institutions during the clinical data collection period 2)Patients who are 20 years or older at the time of registration (no age-upper limit) 3)Patients who receive dialysis in modes other than ECUM (UF) during the clinical data collection period 4)Patients who undergo a routine blood test at least once a month as part of regular medical treatment during the clinical data collection period

Exclusion criteria

Exclusion criteria: 1)Patients who use continuous ambulatory peritoneal dialysis (CAPD) together during the clinical data collection period 2)Patients who are judged inappropriate for inclusion in this study by the investigators

Design outcomes

Primary

Measure	Time frame
Accuracy of fluid removal Incidence of adverse events and malfunctions	—

Countries

Japan

Contacts

Public ContactTakuya Otsuka

Toray Medical Company Limited Dialysis Division Technical Service Division Technical Sales Dept.

Takuya_Ootsuka@tmc.toray.co.jp055-925-5320

Outcome results