Preclinical external compression in pelvic injuries

Preclinical external compression in pelvic injuries - pelvic2bind

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00017683

Enrollment

500

Registered

2019-09-27

Start date

2019-10-14

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

S32.7 R57.1

Interventions

Group 1: Peer Physicians from 26 countries will be asked about their proceedings and experiences with pelvic binders

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Physicians that are charged with the in-house treatment of severly injured patients

Exclusion criteria

Exclusion criteria: nonparticipation

Design outcomes

Secondary

Measure	Time frame
The trial seeks to elucidate experience and use of pelvic binders in pelvic injuries by physicians in an internet-based questionnaire. Therefore no typical primary and secondary outcomes.	—

Primary

Measure	Time frame
To elucidate the regional difference in standard operating procedures and infrastructure in preclinical and intraclinical treatment of pelvic injuries.	—

Countries

Cyprus, Czechia, Denmark, Estonia, France, Georgia, Germany, Ghana, Greece, Hungary, Ireland, Israel, Italy, Jamaica, Kenya, Lithuania, Moldova, Netherlands, Norway, Portugal, Slovenia, South Africa, Spain, Sweden, Switzerland, United Kingdom

Contacts

Public ContactChristoph Wölfl

Marienhaus Klinikum Hetzelstift

christoph.woelfl@marienhaus.de06321-859-2006

Outcome results

None listed

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