Evaluation of postoperative outcomes and quality of life in patients with arterial-popliteal compression syndrome

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035480

Enrollment

Registered

2024-11-29

Start date

2024-12-20

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

popliteal entrapment syndrome, arterial-popliteal compression syndrome I77.1

Interventions

Group 1: Retrospective study of the surgical treatment and prospective evaluation of the postoperative quality of life of patients with arterial-popliteal compression syndrome who were treated surgica

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patient's ability to give consent, surgical treatment due to a PAE has taken place

Exclusion criteria

Exclusion criteria: Underage patients, patients unable to give consent

Design outcomes

Primary

Measure	Time frame
Prospective determination of disease-specific quality of life using a questionnaire (EQ-5D-5L), as well as determination of symptoms that typically occur in patients with arterial-popliteal compression syndrome (walking distance restriction, pain at rest, trophic disturbance)	—

Secondary

Measure	Time frame
Determination of procedure-associated success, as well as freedom from revision surgery, reintervention-free survival, leg preservation and survival in general.	—

Countries

Germany

Contacts

Public ContactAndreas Peters

Universitätsklinikum Heidelberg

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

Outcome results

None listed

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