Pain, Acute Clinical Trial
Official title:
Comparison of the Effectiveness in Pain Reduction Between a Rib Splint Produced in the ER and a Manufactured Rib Splint: Preliminary Clinical Study
A pilot study for a prospective randomized clinical trial was conducted to compare subjects
using the CCO (Group-A) with those using the ER-splint (Group-B) before and after the
intervention.
The primary outcome was difference in the level of pain based on the visual analogue scale
(VAS) between before and after intervention in each group during forceful and resting
respiration.
VAS : Visual analogue scale CCO : Chrisofix® Chest Orthosis
Investigators performed VAS assessments to determine the level of pain in the subjects with
RFs during resting and forceful respiration. Investigators applied either the CCO rib splint
or the ER splint to the RF subjects in a randomized order. At 30 minutes after splint
application, investigators repeated the VAS assessments during resting and forceful
respiration. Subsequently, additional pain control was provided via intravascular drug
injection.
RF : Rib fractures VAS : Visual analogue scale CCO : Chrisofix® Chest Orthosis
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