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NCT02802774 · ClinicalTrials.gov registry record · NA

Immobilization of Postoperative Distal Radius Fractures

A NA study, sponsored by University of California, San Francisco.

Terminated
Registry status
NA
Development phase
20
Enrollment target

NCT02802774 is a NA study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 20 participants.

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The verdict

NCT02802774, a NA study, was terminated before completion, sponsored by University of California, San Francisco.

TERMINATED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

The management of distal radius fractures has been in a state of evolution over the past 30 years. Treatment has become increasingly focused on obtaining a stable, internal construct for quick return to normal, daily activities. With the advent of volar locking plates, the wrist fracture is stable before the patient leaves the operating room. As surgical plate and screw constructs become more stable, the need for casting and splinting may be less. The presumptive "next step" in operative management of distal radius fractures is to do away with the postoperative splint. A review of the available English language literature failed to reveal any studies evaluating the use of postoperative splinting and patient outcomes. This prospective, randomized study was designed to investigate the use of temporary plaster splints versus removable over-the-counter splits versus soft dressings for post-operative treatment of extra-articular and intra-articular distal radius fractures. The patients will be followed for 12 months evaluating maintenance of fracture reduction and patient outcomes.

Interventions

  • OTHER Plaster Splint
  • OTHER Velcro Brace
  • OTHER Soft Dressing

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2016-07
Est. Completion 2020-04-19
Phase NA

What the Registry Record Tells You About NCT02802774

The ClinicalTrials.gov registry entry for NCT02802774 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Plaster Splint is the first listed.

NCT02802774 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02802774 about?

NCT02802774 is a clinical study titled "Immobilization of Postoperative Distal Radius Fractures". The management of distal radius fractures has been in a state of evolution over the past 30 years. Treatment has become increasingly focused on obtaining a stable, internal construct for quick return to normal, daily activities. With the advent of volar locking plates, the wrist fracture is stable b...

What is the current status of trial NCT02802774?

This trial is currently terminated. It is a NA study. The enrollment target is 20 participants. The study started on 2016-07. Estimated completion is 2020-04-19.

What interventions are being tested in trial NCT02802774?

The interventions under investigation include: Plaster Splint (OTHER), Velcro Brace (OTHER), Soft Dressing (OTHER).

Who is sponsoring clinical trial NCT02802774?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.