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Clinical Trial Summary

The purpose of this study is to compare early return to function in patients treated with closed reduction percutaneous pinning and open reduction internal fixation in displaced fractures of the distal radius.

Hypothesis: Wrist range of motion, grip strength and outcome at 2-3 months after injury are better in patients treated with open reduction, internal fixation (ORIF) than in patients treated with closed reduction percutaneous pinning techniques (CRPP). In addition patients treated with ORIF return to work at faster rates.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00828685
Study type Interventional
Source Beth Israel Deaconess Medical Center
Contact
Status Completed
Phase N/A

See also
  Status Clinical Trial Phase
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Not yet recruiting NCT05943340 - Shoulder Proprioceptive Training During Immobilization of the Wrist N/A
Completed NCT02608801 - Prediction and Secondary Prevention of Fractures
Completed NCT00285961 - Evaluation of Cork Splint Materials Instead of Plaster Splint for Children N/A