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Sens-AVK-Study

Sens-AVK-Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033683
Enrollment
150
Registered
2024-03-20
Start date
2024-05-06
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Peripheral arterial occlusive disease, intermittent claudication stages IIa-IIb according to Fontaine/ 1-3

Interventions

Group 1: Patients with peripheral arterial disease receive a sensor and undergo structured walking training 4-6 weeks, 3 months and 6 months after baseline screening. The follow-up ends after 24 month

Sponsors

Universitätsklinikum Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Ability to give informed consent; clinical complaint stage pAVK IIa-IIb acc. Fontaine/1-3 Rutherford; signed informed consent form; willingness for follow-up examinations; endovascular procedure if indicated

Exclusion criteria

Exclusion criteria: Refusal of data collection; discontinuation of the study; patient is unable to give informed consent; open surgical procedure, if indicated; life expectancy < 24 months; treatment-relevant cancer, advanced dementia; stroke with persistent hemiparesis; COPD grade Gold C or D; Parkinson's disease Hoehn and Yahr stages IV - V; severe degenerative joint disease with planned surgery;

Design outcomes

Primary

MeasureTime frame
The data is intended to provide predictive values for determining the best individual therapy method, for determining the optimized use of the various therapy methods and walking distance, and for the quality of the results.

Countries

Germany

Contacts

Public ContactAlina Marilena Bresler

Universitätsklinikum Heidelberg

studienzentrum.gefaesschirurgie@med.uni-heidelbeg.de+49 6221566513

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026