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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03476824
Other study ID # 2017-01859; ch18Ramser
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2006
Est. completion date December 31, 2016

Study information

Verified date March 2023
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the project is to predict the patient under conservative therapy as a function of the patient Classification of Rommens and Hofmann and other potential prognostic factors. A corresponding prognostic score may be used in the future by patients and attending physicians support joint decision between surgical and conservative treatment.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date December 31, 2016
Est. primary completion date December 31, 2016
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - Pelvic fracture after low-energy trauma - Treatment in the years 2006 to 2016 - patients equal to or older than 60 years Exclusion Criteria: - Pelvic fracture after a high-energy space - Pathological fracture in the area of a tumor or a bony metastasis - Existence of a documented refusal

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland University Hospital Switzerland, Traumatology Basel

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality number of patients who died within one year after pelvic fracture from pelvic fracture until year 1
Primary loss of independence loss of independence defined as number of patients leaving their own home and starting to live in a retirement home or asylum within one year after pelvic fracture from pelvic fracture until year 1
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