Clinical outcome after hindfoot arthrodesis vs Burgess amputation

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035964

Enrollment

150

Registered

2025-03-20

Start date

2024-03-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

S88.1

Interventions

Group 1: Retrospective comparison of clinical outcome parameters (using specifically validated scores such as SF12, VAS and return to work) of patients who have undergone Burgess amputation or hindfoo

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Surgical care that took place in the Unfallklinik Frankfurt participate in the study

Exclusion criteria

Exclusion criteria: Surgical care not in the Unfallklinik Frankfurt younger than 18 years Refusal to participate in the study

Design outcomes

Primary

Measure	Time frame
After reviewing 680 patient data from 2012 to 2023 and assessing the inclusion and exclusion criteria, 270 patients remained in the monocentric, retrospective study for evaluation. After a mean follow-up of 5.9 years, the observed time to return to work was the primary endpoint.	—

Secondary

Measure	Time frame
SF 12 questionnaire	—

Countries

Germany

Contacts

Public ContactSebastian Fischer

BG Unfallklinik Frankfurt am Main

dr.sebastian.fischer@me.com+49(0)694750

Outcome results

None listed

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