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AzTrials

Anterior Cruciate Ligament ReconstructionNCT07200700

Inter-rater Reliability of the GNRB Arthrometer

A study testing Knee laxity arthrometer in people with Anterior Cruciate Ligament Reconstruction, run by Vastra Gotaland Region at 1 site in Sweden.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Although clinical examination is commonly used to diagnose an anterior cruciate ligament (ACL) injury, the method is subjective. For many years, the arthrometer KT1000 has been used to verify clinical results, mostly due to its simplicity. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Knee laxity arthrometer
Could I receive a placebo?
No, everyone receives an active treatment
How many people
17 participants
Where
1 siteSweden
Study dates
24 Aug 2020to 20 Dec 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • -

Who cannot join

  • Patients under 18 years of age, and those having had previous surgery to any knee, posterior cruciate ligament (PCL) injury or more severe concomitant injuries to the meniscus and collateral ligaments

Trial locations and contacts

1 site in 1 country.

Sweden1 site
  • NU Hospital Group

    Trollhättan, Europe, 46185

Other trials in Sweden

About this study

Official title: Assessing Knee Laxity and Inter-rater Reliability of the GNRB Arthrometer a Clinical Study of Patients With Anterior Cruciate Ligament Injuries Before and After Reconstruction

Although clinical examination is commonly used to diagnose an anterior cruciate ligament (ACL) injury, the method is subjective. For many years, the arthrometer KT1000 has been used to verify clinical results, mostly due to its simplicity. While the KT1000 is no longer available for purchase, other arthrometers have been introduced, one being the Genoroub (GNRB). The latter has several automatic steps, has been marketed to have a higher reproducibility, and able to detect partial tears.

While the KT1000 and GNRB have previously been compared in several studies, it's mostly been compared in healthy subjects. The current study aim to analyse the results in a clinical environment on injured objects and compare the results both before and after ACL reconstruction. The main hypothesis was that the GNRB offers high inter-rater reliability between two examinors and can replace the KT1000 in the everyday clinical setting.

Read more

Methods Consecutively, 20 patients > 18 years of age, 12 men and 8 women, with an ACL injury scheduled for surgical reconstruction, were included. All patients were screened between August 2020-2021 at the NU Hospital Group in Trollhattan, Sweden. To be eligible, the patients had to present with a first time ACL injury verified by clinical examination with or without an magnetic resonance imaging, a healthy contralateral knee and to not have sustained multi-ligament injuries to the knee. Minor collateral ligament injuries and meniscal and cartilage injuries were included.

All patients received both spoken and written information before signing an informed consent. The study was approved by the Swedish ethical committee.

All patients were examined both pre- and postoperatively, in accordance with local standard protocol, including range of motion, knee laxity measurements (manual Lachman test, pivot shift test) The participants were examined starting with the healthy/uninjured knee. Who of the two examinors started the testing was randomly decided, however alternated at the follow-up. Clinical examination and KT1000 testing were only performed by examiner 2, given the need for experience with the KT1000 for accurate results.

Statistically, a side-to-side difference (SSD) of 3 mm was set to indicate ACL injury according to general concensus. For the dichotomous values, an SSD of ≥3 mm was considered a yes to ACL injury and <3mm a no, respectively, for both the GNRB and the KT1000.

A power analysis was performed estimating a difference of 1 mm between examiners with an SD of 1 mm, resulting in 17 patients needed to reach a power of 80% with a significance level of 0.05.

As for the inter-rater reliability, the intra-correlation coefficient (ICC) was calculated and considered poor (<0.5), moderate (0.5-0.75), good (0.75-0.9) or excellent (>0.9).

Being tested
Knee laxity arthrometer
Keywords
Anterior cruciate ligament reconstruction, arthrometers, GNRB, KT1000, knee laxity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Knee laxity arthrometerDiagnostic test

    Inter-reliability analysis of the GNRB arthrometer between two examinors compared to standard KT 1000 arthrometer

Study groups in NCT07200700
Study groupRoleWhat they receive
GNRB arthrometerOtherReliability testing GNRB arthrometer between two examinors
Receives: Diagnostic Test: Knee laxity arthrometer

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Identifying anterior knee translation in patients with anterior cruciate ligament injury before and after reconstruction compared to the contralateral non-injured knee

    Measuring anterior knee translation in both injured and non injured knee before and after reconstruction using two different devices; GNRB and KT 1000 arthrometer

    Measured: Primary measurement pre operative, secondary measurement 6-12 months after reconstruction

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Oct 2025
  2. Study start24 Aug 2020
  3. Primary completion20 Dec 2022
  4. Study completion20 Dec 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Model description
Inter-reliablility study
Masking
None (open label)
Enrolment
17 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07200700
Sponsor's protocol ID
Dnr 2020-02062
Status last verified
Sep 2025
First submitted
15 Sep 2025
Last updated
1 Oct 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: As the study is a part of future thesis data will be available in this publication

Questions about this trial

What is this clinical trial studying?

A study testing Knee laxity arthrometer in people with Anterior Cruciate Ligament Reconstruction, run by Vastra Gotaland Region at 1 site in Sweden.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Identifying anterior knee translation in patients with anterior cruciate ligament injury before and after reconstruction compared to the contralateral non-injured knee (time frame: Primary measurement pre operative, secondary measurement 6-12 months after reconstruction). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Oct 2025.

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