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Creating a Diagnostic Decision Rule for Shoulder Injury: CASH-trial

Z

Zaans Medisch Centrum

Status

Unknown

Conditions

Trauma

Treatments

Other: Standard diagnostic item list

Study type

Interventional

Funder types

Other

Identifiers

NCT02857439
CASH Zaansmc

Details and patient eligibility

About

What combination of ≤ 6 clinical variables will give the highest specificity for indicating significant shoulder injuries (fractures or dislocations) with a set sensitivity of ≥ 97%?

Although shoulder trauma is a common injury, there is no clinical decision rule to determine the necessity for radiography for these traumas. With this trial the investigators aim to develop such a rule to reduce the amount of radiographs without missing any significant injuries.

The primary objective is to compose a set of clinical diagnostic criteria predictive of shoulder fractures or dislocations that would reduce the amount of radiographs without missing any significant injuries. A second objective is to determine if the clinical decision rule is applicable for triage use.

Full description

The CASH (Clavicle-AC-Joint-Sub-capital-Humerus) trial is designed as a cross sectional interobserver study. It will randomize between first examiner of the patient to determine applicability for triage use and use a list of 19 criteria to determine a clinical decision rule for significant shoulder injuries.

Method/intervention After admittance to the ED, all consecutive shoulder injury patients will be assessed for eligibility in the study. After informed consent is given, the patient will be randomized for first observer (ED physician or triage nurse) to be examined, which means they will be assessed in duplo.

The patient will be examined by means of a score form, which contains 19 different diagnostic criteria. The criteria are grouped: anamnesis, inspection, palpation and pain/range of motion(ROM). After completing the list, patients will get a full set of shoulder x-rays: shoulder AP- and axial-view, and clavicle AP and 30' cranio-caudal view.

The trial participation for the patient will be completed at this point and final diagnosis and treatment are provided by the ED physician according to his/her own findings and interpretation of the radiographs. For the study, the radiographs will be reassessed by one consultant radiologist specialized in skeletal trauma.

Enrollment

280 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged18-65 years
  • Trauma <48h

Exclusion criteria

  • Any prior ipsilateral shoulder surgery.
  • Any diseases of the bones potentially influencing fracturability (osteogenesis imperfecta, osteoporosis, achondroplasia, M. Kahler, chronic (> 1yr) prednisone use > 5mg)
  • Any shoulder injury as part of a multi-trauma or high energy trauma (HET) with distractible injuries
  • Any condition that will influence the perception of pain (e.g. alcohol intoxication, psychiatric problems, mental retardation)

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

280 participants in 2 patient groups

MD as first examiner
Other group
Description:
Patients will be examined according to a standardized physical examination item list
Treatment:
Other: Standard diagnostic item list
Triage nurse as first examiner
Other group
Description:
Patients will be examined according to a standardized physical examination item list
Treatment:
Other: Standard diagnostic item list

Trial contacts and locations

1

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Central trial contact

Kim Rijsbergen, BSc; Robert Jan Derksen, MD

Data sourced from clinicaltrials.gov

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