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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03556514
Other study ID # 2017-05-009AC
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 10, 2017
Est. completion date May 9, 2019

Study information

Verified date June 2017
Source Taipei Veterans General Hospital, Taiwan
Contact Jung-Pan Wang, M.D.,Ph.D.
Phone 02-28757557
Email jpwang801@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The current status of the disease under study. Including natural history, disease prognosis.

Distal radial fractures (DRF, distal radius fractures) are the most common fractures, allowing the user to lock the steel plate to accelerate the recovery of the wrist, but related injuries such as the triangular fibrocartilage cartilage complex (TFCC) tear or distal radius ulna joint (DRUJ) ligament tear with DRUJ instability requires time fixed or further repair surgery. If these issues are ignored, there will be weakness in the future. The ulnar shortening commonly used by hand surgeons is to improve the damage of TFCC or DRUJ instability. In the case of distal radial fracture combined with DRUJ instability, it is not clear that the distal radial fracture combined with DRUJ instability patients has long-term prognosis.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date May 9, 2019
Est. primary completion date May 9, 2019
Accepts healthy volunteers No
Gender All
Age group 24 Years and older
Eligibility Inclusion Criteria:

- Outpatient following for at least one year

Exclusion Criteria:

- (1) Injury or arthritis before; (2) Open fractures, or more wounds require surgery

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Taipei Veterans General Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Taipei Veterans General Hospital, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary 4-Item Pain intensity Measure Each item is scored 0-10(0=no pain;10=pain as bad as can be) 5 seconds
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