The goal of this clinical trial is to assess patient reported outcome measures of adult patients who are diagnosed with a distal radius fracture and treated with a patient-specific 3D printed splint as compared to a control cohort. Patients receive routine immobilization procedure with a patient-specific 3D printed splint instead of the use of a conventional forearm splint after one week of conventional immobilization. The main study parameters are patient reported outcome measures related to comfort and satisfaction of the medical aid. This will be measured qualitatively with a semi-structured interview and quantitively using questionnaires.
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D-QUEST
Timeframe: three to five weeks post injury
CSD-OPUS
Timeframe: three to five weeks post injury
EQ-5D VAS
Timeframe: three to five weeks post injury
Semi structured interview
Timeframe: three to five weeks post injury