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Posttraumatic osteoarthritis following perilunate (fracture) dislocations

Posttraumatic osteoarthritis following perilunate dislocations and perilunate fracture dislocations in young patients and the correlation with subjective and objective outcome measures. A descriptive cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON21645
Enrollment
30
Registered
2015-08-24
Start date
2015-08-01
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

posttraumatic osteoarthritis perilunate dislocation/fracture outcome

Interventions

No intervention. Questionnaires: PRWE, DASH, SF-36 and MHQ. X-rays of both hands. Range of motion test and grip strength test by a certified handphysician

Sponsors

University Medical Center Groningen; C.M.Lameijer C.K. van der Sluis
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients treated in the period 1996 until 2014 in the University Medical Center Groningen for a PLD-PLFD - 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) - Written informed consent - Mentally competent

Exclusion criteria

Exclusion criteria: Preexistent osteoarthritis of the hand or preexistent declined function of the hand or 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
The prevalence of posttraumatic osteoarthritis.

Secondary

MeasureTime frame
Patient reported functional outcomes objectified with the PRWE, DASH, SF-36 and MHQ. Objective outcomes: X-rays, range of motion, grip strength.

Contacts

Public ContactC.M. Lameijer

Medical Center Groningen Hanzeplein 1

C.M.Lameijer@umcg.nl+31628425094

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)