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The implementation of a new form of dialysis at the dialysis department of the Albert Schweitzer Hospital, Dordrecht, the Netherlands

An observational study into quality of hemodialysis in the Dialysis Department of the Albert Schweitzer Hospital, the Netherlands

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN17138470
Enrollment
100
Registered
2021-12-09
Start date
2024-01-31
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Hemodialysis Not Applicable

Interventions

Current intervention as of 03/05/2022: The nephrologists of the Albert Schweitzer Hospital have decided to change standard haemodialysis treatment in the near future. The study will observe standard p

Sponsors

Albert Schweitzer Ziekenhuis
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: HD(F) patients at the Dialysis Department of the Albert Schweitzer Hospital, Dordrecht, The Netherlands

Exclusion criteria

Exclusion criteria: Does not meet the inclusion criteria

Design outcomes

Primary

MeasureTime frame
Current primary outcome measure as of 03/05/2022: Quality of the subsequent treatments measured using the statistical difference between the following parameters: 1. Values of laboratory tests including bone densitometry which are taken routinely according to the protocol in force before and after dialysis treatment 2. Dialysis readings that are taken routinely and are available in the dialysis machine including clock time, weight, blood pressure, pulse rate, dialysance clearance, ultrafiltration rate, arterial and venous pressure of the dialysis machine, and transmembrane pressure before and after each dialysis session; and blood flow rate, ultrafiltration achieved, and clotting in the dialyzer and venous chamber after rinsing with 300 ml NaCl 0,9% solution at the end of each dialysis session. Red colouring is scored by visual inspection by the nurse. Scoring is as follows: 0 no red fibers, 1 is less than 10% of fibers are red, 2 is more than 10% but less than 50% of fibers are red, 3 is more than 50% of fibers are red. 3. Dose of relevant medications used (relevant medication includes all medication with an effect on Ca- and Mg-balance, anticoagulation, erythropoietin, and iron suppletion) extracted from the hospital information system (HiX) by the Company Information Centre (BIC) before and after dialysis treatment 4. Number of blood transfusions given measured using details of blood transfusions which are registered in the hospital system Diamant at the time of transfusion Current primary outcome measure as of 28/04/2022: The quality of the subsequent treatments measured using the statistical difference between following parameters before, during and after dialysis: 1. Values of laboratory tests which are taken routinely 2. Dialysis readings that are taken routinely like clock time, weight, blood pressure, pulse rate, dialysance clearance, ultrafiltration rate, arterial and venous pressure of the dialysis machine, transmembrane pressure, blood flow rate, ultraf

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

Netherlands

Contacts

Public ContactG.M.T. de Jong
g.m.t.de.jong@planet.nl+31 (0)653591054

Outcome results

None listed

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