ClinicalTrials.gg
CompletedNCT03396965Updated Jan 16, 2018

Mini-C-Arm for Distal Radius Fractures in Adults

An interventional study of Mini-c-arm in Distal Radius Fracture, sponsored by University of Cincinnati. Completed. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-01-16.

Sponsored by University of Cincinnati · Not applicable, Interventional, and Treatment

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Phase
Not applicable
Study type
Interventional
Enrollment
63
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Determine efficacy of the use of mini-c-arm fluoroscopy for the closed reduction of isolated distal radius fractures in adult patients in the emergency department setting.

02

Conditions studied

  • Distal Radius Fracture

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03

In context

Wrist Fractures

330 studies on the registry are indexed under Wrist Fractures; 72 are open to participants now.

This study's enrollment of 63 is close to the median of 63 across 265 interventional studies indexed under Wrist Fractures.

Browse Wrist Fractures studies →

Lead sponsor

University of Cincinnati is the lead sponsor of 324 studies on the registry; 42 are open to participants now.

Of its 24 completed or terminated interventional studies of FDA-regulated products, 15 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Closed distal radius fracture requiring reduction

Exclusion criteria

Exclusion Criteria:

  • Open, other ipsilateral upper extremity fractures, pregnant, incarcerated, less than 18 yo
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Single (Outcomes assessor)
Enrollment
63 participants (actual)

Study arms

  • Experimental
    Mini-c-arm

    Fluoroscopically aided reductions

    Other: Mini-c-arm

  • No intervention
    Standard

Interventions

  • OtherMini-c-arm

    Fluoroscopy used to aid reduction of distal radius fracture

06

What researchers measure

Primary outcomes

  1. Reduction quality

    Fracture alignment measured on post-reduction radiographs

    Time frame: Immediately post reduction

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of May 2015, a primary completion of May 2017 and a completion of May 2017. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 5, 2018
First posted
Jan 11, 2018
Start
May 2015
Primary completionActual
May 2017
CompletionActual
May 2017
Last update
Jan 16, 2018
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 16, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03396965
Responsible party
Steven Dailey (Principal Investigator, University of Cincinnati) — Principal investigator
First posted
Jan 11, 2018
Start date
May 2015
Primary completion
May 2017
Completion
May 2017
Last update
Jan 16, 2018

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2018. You cannot join it, but the record below documents what was studied.

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