Strategies in case of failed kyphoplasty

Strategies in case of failed kyphoplasty - SFK

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00000366

Enrollment

150

Registered

2013-01-10

Start date

2010-08-17

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

M84.48

Interventions

Group 1: All patients undergoing Kypho- or Vertebroplasty will be included and the quality of life assessed by the SF12 and the Euroquol5D. The function will be measured with the ODI. Strategies in ca

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: all patients tretaed by kyphoplasty older than 18 years

Exclusion criteria

Exclusion criteria: patients without Kyphoplasty, and under 18 years

Design outcomes

Primary

Measure	Time frame
Primary endpoint of the study is quality of life measured by the EuroQuol 5D comparing patients after kyphoplasty with or without secondary interventions. The patients will be called and/or sent a letter with the following further questionnaires (secondary endpoint): short form 12 (SF12) also for quality of life, Oswestry Disability Index (ODI) for function.	—

Secondary

Measure	Time frame
risc factors for secondary intervention	—

Countries

Germany

Contacts

Public ContactHagen Schmal

Dep. Orthopädie und Traumatologie Universitätsklinik Freiburg

hagen.schmal@freenet.de+49 761 270 90160

Outcome results

None listed

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