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Osteoarthritis following distal radius fractures in young patients.

Posttraumatic osteoarthritis following distal radius fractures in young patients and the correlation with subjective and objective outcome measures.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON22608
Enrollment
80
Registered
2013-05-20
Start date
2013-09-01
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Radius Fracture Osteoarthritis Subjective

Interventions

- 4 X-rays, 2 of both wrists
- Validated questionnaires (DASH, PRWE, MHQ and SF-36)
- Functional ourtcome (i.e. ROM, grip strength)

Sponsors

Prof. dr. C.K. van der Sluis, MD PhD C.K.van.der.Sluis@umcg.nl
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - All patients treated in the period 2005 until 2011 at the Medical Center Leeuwarden; - All distal radius fractures, AO type A, B and C ; - Men between the ages of 18 - 50 years and women between the ages of 18 - 40 years at the time of injury (no clinical osteoarthritis according to current available information in the literature [21,22]); - Mentally competent; - Living in the Netherlands and sufficient control of the Dutch language; - Availability of X-rays of the wrist of the date of injury and 6 weeks after the injury.

Exclusion criteria

Exclusion criteria: - Fracture treated surgically after the 7th day following initial injury; - Open fractures; - Preexistent osteoarthritis of the wrist or preexistent declined function of the wrist according to the patient; - ASA III-V patients or other contra-indications for surgical treatment at the time of injury. These patients are not able to receive the most optimal treatment and thus altered outcome measures can be expected; - No permanent residency (in the Netherlands); - Co-morbidity that may influence the outcomes, such as neurological of rheumatic disorders influencing arm function; - Insufficient control of the Dutch language; - No informed consent; - Osteoporosis known from medical history; - Pregnant women.

Design outcomes

Primary

MeasureTime frame
(Level of) posttraumatic osteoarthritis.

Secondary

MeasureTime frame
- Subjective outcome measures with validated questionnaires. - Objective outcome measured with functional outcome.

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)