Z49.0
Conditions
Interventions
Group 1: Not applicable, as no intervention takes place (apart from a blood sample as part of the routine and collection of a questionnaire). Only a database is set up.
Sponsors
Universitätsklinikum Augsburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with chronic, terminal renal insufficiency and an existing indication for mandatory hemodialysis
Exclusion criteria
Exclusion criteria: Post renal transplant Peritoneal dialysis Passenger, acute renal insufficiency Daily body temperature (measured in ear) >38°C Septic phlebitis Severe cognitive impairment Temporary need for dialysis Lack of artery or vein required for the application
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Establishment of a data documentation system for the documentation of epidemiological, procedural and postoperative data. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Collection of epidemiological data on patients with end-stage renal disease at the CNHU-HKM - Establishment of a digital patient database at the CNHU-HKM for prospective data collection and long-term data retention - Comparison of epidemiological, procedure-related and follow-up data for hemodialysis shunts between the UKA and the CNHU-HKM (prospective data collection/matched pairs analysis). - Determination of quality of life in patients with trminal renal insufficiency at both hospitals using a standardized questionnaire (EQ-5D-5L, EQ-VAS score) - Determination of the duration and frequency of hemodialysis and comparison between patients at UKA and CNHU-HKM (matched pairs analysis). - Determination of the frequency of surgical revisions after AV shunt placement in both countries. Translated with DeepL.com (free version) | — |
Countries
Benin, Germany
Contacts
Public ContactAlexander Hyhlik-Dürr
Universitätsklinikum Augsburg, Klinik für Gefäßchirurgie und endovaskuläre Chirurgie
Outcome results
None listed