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Clinical Trials/NCT00828685
NCT00828685CompletedNot Applicable

Early Functional Outcomes After Closed Reduction Percutaneous Pinning vs. Open Reduction Internal Fixation of Distal Radius Fractures: A Prospective Randomized Trial

Beth Israel Deaconess Medical Center1 site in 1 countryStarted: January 26, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Locations
1
Primary Endpoint
Wrist range of motion measurement. As well as recorded score from the DASH questionnaire.

Study Overview

Brief 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.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •18 years or greater
  • •Patient functions independently
  • •Dorsally displaced, extra-articular fracture (Colles' fracture); or simple intra-articular fracture with a single split between the scaphoid and lunate facets.
  • •Isolated injury (no other injuries).
  • •One of the following criteria:
  • •Substantial initial displacement
  • •Greater than 20 degrees dorsal angulation of the articular surface on the lateral view.
  • •Greater than 100% loss of apposition.
  • •Greater than 5 millimeters of shortening by ulnar variance on the posteroanterior radiograph.
  • •Greater than 2 millimeters articular incongruity (step or gap).
  • •Both dorsal and volar comminution. Inadequate initial manipulative reduction
  • •Greater than 5 degrees of dorsal angulation of the articular surface on the lateral radiograph.
  • •Greater than 3 millimeters of radial shortening by ulnar variance on the posteroanterior radiograph.
  • •Greater than 2 millimeters articular incongruity.
  • •Bayonett apposition of the volar cortex.
  • •Less than 15 degrees of ulnarward inclination of the articular surface in the posteroanterior radiograph. Loss of reduction within 3 weeks of injury.
  • •Any of the following changes in alignment from the initial post- reduction radiographs qualify:
  • •5 degrees or greater loss of palmar tilt of the articular surface on the lateral radiograph.
  • •2 millimeters or greater loss of radial height by ulnar variance on the posteroanterior radiograph.
  • •5 degrees or greater loss of ulnarward inclination of the articular surface of the distal radius on the posteroanteriorradiograph.
  • •2 millimeters or greater articular incongruity.

Exclusion Criteria

  • •More complex articular fractures (i.e. anything more than a simple sagittal split between the scaphoid and lunate facets).
  • •Volarly displaced fractures.
  • •Infirm patients.
  • •Patients that rely on others for basic functional activities.
  • •Open fractures
  • •Fractures associated with neurovascular injury.
  • •Fractures associated with major head, neurological, or visceral injuries that will inhibit the ability to participate in a structured exercise program.
  • •Associated musculoskeletal injuries to the same arm.

Arms & Interventions

Operative (CRPP)

Active Comparator

If indicated, the wrist fracture would be treated with surgery-the specific operative procedure would be randomized.

Intervention: CRPP (Procedure)

Operative (ORIF)

Active Comparator

If indicated, the wrist fracture would be treated with surgery-the specific operative procedure would be randomized

Intervention: ORIF (Procedure)

Outcomes

Primary Outcomes

Wrist range of motion measurement. As well as recorded score from the DASH questionnaire.

Time Frame: 3 months post surgery

Secondary Outcomes

  • Range of motion measured in wrist and a scored DASH questionnaire(1 year after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tamara Rozental

Associate Professor of Orthopedic Surgery

Beth Israel Deaconess Medical Center

Study Sites (1)

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