Methods to determine the dialysis dose in clinical application

Methods to determine the dialysis dose in clinical application - MeDos

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00000499

Enrollment

1000

Registered

2010-07-27

Start date

2007-10-15

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

Z49

Interventions

Group 1:

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Adult haemodialysis patient - Signed informed consent - Physical and mental ability to participate in the study - Double-needle dialysis - Haemodialysis or on-line Haemodiafiltration

Exclusion criteria

Exclusion criteria: - Pregnancy in case of female patient - Pace maker - Implanted pump - Major amputation of arm or leg

Design outcomes

Primary

Measure	Time frame
Simultaneous determination of dialysis dose with 3 different methods (Kt/V_Dau, KtV_OCM, Kt/V_BCM) once in each haemodialysis patient	—

Secondary

Measure	Time frame
Hydration status of haemodialysis patients by single BCM measurement	—

Countries

Czechia, Germany

Contacts

Public ContactRalf Wojke

Fresenius Medical Care Deutschland GmbH

ralf.wojke@fmc-ag.de+49 6172 6092316

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026