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Robot or surgeon? study tests which knee surgery lasts longer

NCT ID NCT00782444

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 192 people aged 50-85 with knee arthritis who needed knee replacement surgery. Half had computer-navigated surgery and half had the traditional technique. The goal was to see if computer guidance helps the new knee last longer, improves function, or reduces complications. Researchers used special X-rays and scans to track implant movement and predict long-term success.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

192 people

The number who actually took part.

Start date

Jan 2009

Finished

Jan 2023

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

50 to 85 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * men and women age 50-85 years old * primary and secondary knee osteoarthritis * rheumatic arthritis of the knee * well compensated heart or lung disease(ASA-grad 1-3) * patients recruited from orthopaedic departments at Haugesund hospital og Haugesund Sanitetsforenings Revmatismesjukehus, Haukeland university hospital, Lovisenberg Diakonale hospital * informed consent * MMS-score \> 20 elir. , tas MMS også dag 2 * Hb \> 11,5 for women and Hb \> 13 for men Exclusion Criteria: * advanced systemic disease * general or local infection * neurological or myogenic disease * Paget's disease of bone * bone cysts in the tibia or femur \> 2 cm in diameter and within 2 cm from the articular surface * liver disease * uncontrolled haematological disease * B-TRC \< 165 * B-Hb \< 11,5 for women * B-Hb \< 13 for men * cancer * uncontrollable heart or lung disease (ASA-class 4) * dementia * immobile hips * hip replacement in ipsilateral hip * knee injury \< 1år earlier * metal allergy * extreme valgus deformity \> 15 degrees or curvature of the tibia, necessitating extramedullary device * earlier fracture of the femur makes it impossible to use intramedullary rod Osteotomy of the proximal tibia og distal femur * BMI \> 35 * Only one knee recruited per patient

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Haugesund hospital

    Haugesund, 5504, Norway

  • Haugesund sanitetsforenings revmatismesykehus

    Haugesund, Haugesund, 5504, Norway

  • Haukeland university hospital

    Bergen, 5021, Norway

  • Lovisenberg diakonale sykehus

    Oslo, Oslo, 0456, Norway

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