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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01857570
Other study ID # NL43482.091.13
Secondary ID
Status Completed
Phase N/A
First received May 10, 2013
Last updated May 13, 2015
Start date June 2013
Est. completion date May 2015

Study information

Verified date May 2015
Source Radboud University
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate whether standard volume computed tomography (CT) has impact on treatment in patients with suspicion of fractures of the wrist and carpus.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date May 2015
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients (18 years and older) who are referred to our hospital for conventional radiography of the wrist and carpus

- Recent trauma mechanism (within 3 days before presentation)

- Clinical suspicion of fractures of the wrist and carpus. The carpus includes all carpal bones, but does not include the metacarpal bones.

Exclusion Criteria:

- Patients who were not evaluated by a clinician before imaging was performed.

- Open fractures

- No informed consent or no prospective data collection could be obtained. Informed consent cannot be obtained in case patients do not speak or understand Dutch.

- Patients who cannot be positioned in upright position, immobilized on a spine board or transferred to the intensive care unit and cannot undergo upright CT

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Radiation:
Volume Computed Tomography of the wrist and carpus


Locations

Country Name City State
Netherlands Radboud University Nijmegen Medical Centre Nijmegen

Sponsors (1)

Lead Sponsor Collaborator
Radboud University

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Other Radiological feasibility Image quality (5-point scale), artifacts (5-point scale) noise (standard deviation Hounsfield Units), radiation dose, and presence of technical problems Within an average of three days after CT No
Other Patient outcome: Pain and disability Pain and disability according to the "Patient rated wrist and hand evaluation (PRWHE) score" 6 weeks, 6 months, and 12 months after trauma one year No
Primary Proportion of patients with prospectively documented treatment changes after CT This endpoint is defined as presence of difference in predefined treatment regimens before and after CT. These regimens include:
-Conservative treatment on the emergency ward (functional, immobilization with bandage, cast, or closed reduction and cast), closed operative treatment (reduction and cast on operation room, percutaneous pinning, or external fixation), open surgical treatment (dorsal, radial, or palmar exposure with reduction and internal fixation).
Additional regimens include: Second opinion from a colleague or consulting a different specialism.
within same visit (i.e. in one day) No
Secondary Diagnostic performance of CT and conventional radiography (CR) for fracture pattern Fracture patterns are classified according to presence and type of fractured bones, presence of intra-articular components of distal radius fractures (including sigmoid notch involvement), presence of (fracture) dislocation or avulsion fractures of carpal bones. Standard of reference is presence of injuries at imaging, at surgery, and disability complains at 1-year follow up. In case of discrepancy, consensus will be reached at the end of the study by a panel of trauma surgeons and radiologists. within the same visit (one day) No
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