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Motec Versus Remotion Total Wrist Arthroplasty - A Prospective Study

Motec Versus Remotion Total Wrist Arthroplasty - A Prospective Randomized Study.

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01842724
Enrollment
40
Registered
2013-04-30
Start date
2014-08-31
Completion date
2034-11-30
Last updated
2024-02-28

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

Conditions

Non-rheumatoid Wrist Arthritis

Brief summary

The purpose of this study is to determine the difference in the results between Motec and Remotion wrist arthroplasty in the treatment of non-rheumatoid wrist arthritis.

Interventions

PROCEDUREMotec total wrist arthroplasty
PROCEDURERemotion total wrist arthroplasty

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years

Inclusion criteria

* Patients with painful non-rheumatoid wrist arthritis (posttraumatic arthritis and late stage Kienboeck's disease) * Age 18-70 years * ASA class 1-3

Design outcomes

Primary

MeasureTime frameDescription
PRWHE (Patient rated Wrist and Hand Evaluation score)24 months postopPRWHE is a wrist specific patient assessed questionnaire, measuring pain, wrist specific function and general function

Secondary

MeasureTime frameDescription
Grip Strength24 months postop
Pain in affected wrist24 months postopVisual analogue scale
Quick-DASH24 months postopDisabilities of the Arm, Shoulder and Hand questionnaire
intraoperative complicationsintraoperative
Wrist movement24 months postopOverall degree of flexion, extension, radial and ulnar deviation
Implant loosening24 months postopImplant loosening seen on x-ray
Implant migration24 months postopImplant migration seen on model-based roentgen stereophotogrammetric analysis (RSA), as a possible precursor of later implant loosening
Periprosthetic bone mineral density24 months postopBMD measured with DEXA (dual-energy x-ray absorptiometry)
Reoperations24 months postopReoperations of any cause
Postoperative complications24 months postop

Countries

Norway

Outcome results

None listed

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