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Exploration of Wrist Soft Tissue Injuries Associated With Wrist Fractures

Exploration of Acute TFCC-injuries in Association With Distal Radius Fractures

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01145716
Enrollment
20
Registered
2010-06-17
Start date
2009-08-31
Completion date
2011-05-31
Last updated
2011-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Triangular Fibrocartilage Complex Injuries

Keywords

TFCC injuries, Distal radius fractures

Brief summary

The purpose of this study is to describe and stage lesions of the triangular fibrocartilage complex (TFCC) in association with distal radius fractures. 20 patients with dorsally dislocated AO type A fractures of the distal radius with sufficient displacement (based of cadaveric data) will be included. After stability testing and wrist arthroscopy. The TFCC is explored through a volar incision and injuries were documented and repaired from this approach.

Interventions

PROCEDUREArthroscopy, surgery

Ulno-volar wrist approach to the TFCC

Sponsors

Linkoeping University
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-65 * Distal radius fracture * Displacement \> 20 degrees of dorsal angulation

Exclusion criteria

* Previous significant wrist injury * Declines to participate * Ulnar styloid fracture at base or proximal to it

Design outcomes

Primary

MeasureTime frameDescription
Residual instability symptomsApprox 2-6 months to include the patients that meet the inclusion criteria. They will be followed for 6 momthsMechanisms of injury are poorly previously described. This study will hopefully confirm cadeveric data. There is some evidence that patients might benefit from acute repair. Residual instability can be both ulnocarpal and radioulnar.

Secondary

MeasureTime frameDescription
Adverse eventsThree monthsPatients that accept to participate will undergo exploration from a (new) ulnovolar approach. The study is purely descriptive. Patients are monitored for adverse events such as nerve injury and infection for 3 months.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026