Skip to content

Sheffield Multiple Rib Fractures Study:

Sheffield Multiple Rib Fractures Study: Evolution of Classification, Management and Outcomes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02608541
Acronym
SMuRFS
Enrollment
21
Registered
2015-11-18
Start date
2015-10-12
Completion date
2018-10-16
Last updated
2019-02-26

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

Conditions

Rib Fractures

Keywords

Multiple Rib Fractures, Frail Chest

Brief summary

An observational study to derive clinically relevant and predictive rib fracture classification systems, based on retrospective and prospective cohorts, incorporating assessment of PROMs (Patient Reported Outcome Measures) and healthcare utilisation

Detailed description

The aim of this study is to derive radiology-based classifications of rib fractures and to test whether such classifications have a value in the prediction of clinical outcomes and patient reported outcome measures. The first aspect of work is to analyse existing radiology investigations (plain chest radiography (CXR) and derive classifications of rib fractures that, in the retrospective cohort of operated and non-operated cases, could have potential value in the guidance of management and prediction of clinical outcomes. The second aspect will be to evaluate the feasibility of collection of Patient Reported Outcome Measures in patients suffering multiple rib fractures, which will be used to assess the impact of the radiological classifications. The indications for surgery will remain according to current clinical practice and the management algorithms that have been developed previously in the department.

Interventions

OTHERrib fracture fixation

Use of MatrixRib, where indicated, according to departmental protocol

Sponsors

University of Sheffield
CollaboratorOTHER
Sheffield Teaching Hospitals NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Multiple simple rib fractures * Flail chest

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Acute Painup to 2 yearsVisual Analogue Score

Secondary

MeasureTime frameDescription
Forced Vital Capacity (FVC)up to 2 years
Length of critical care unit stayup to 1 year
Complications during critical care unit stayup to 1 yearadverse events as assessed by CTCAE v4.0
Length of hospital stayup to 1 year
Complications during hospital stayup to 1 yearadverse events as assessed by CTCAE v4.0
Forced Expired Volume in 1 second (FEV1)up to 2 years
Quality of Life - EQ5Dup to 2 yearsEuroQol Group EQ5D
Quality of Life - EORTC (European Organisation for the Research and Treatment of Cancer) QLQ-C30 (Quality of Life Questionnaire - Cancer-30)up to 2 yearsEORTC QLQ-C30
Quality of Life - EORTC QLQ-LC13 (Lung Cancer13)up to 2 yearsEORTC QLQ-LC13
Healthcare costup to 2 yearsprocedural costs plus hospital cost plus community healthcare costs
Quality of Life - SF36 (Short Form 36)up to 2 yearsSF-36

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026