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Status unknownNCT05614297Updated Nov 14, 2022

Agreement Between Rolimeter and Lachmeter in Patients With ACL Injury

An observational study in Anterior Cruciate Ligament Injuries and Laxity of Ligament, sponsored by Region MidtJylland Denmark. Status unknown at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-11-14.

Sponsored by Region MidtJylland Denmark · Observational

The sponsor has not verified this record recently (last verified Nov 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
60
Ages
18 Years and older
Sex
All
01

Study summary

The study is a quality assurance study, aiming to determine the agreement between two different measurement instruments for assessing knee joint laxity in patients with ACL injuries.

The study aims to include 60 patients with previous ACL injury, recruited in an outpatient clinic at Aarhus University Hospital from September 2022 to March 2023. For patients who consent to participate in the study, their knee joint laxity in both the injured and the non-injured knee is assessed using both a Rolimeter and a Lachmeter. Subsequently, the collected data are examined to determined the agreement between the two measurement instruments.

Read the detailed description

Methods:

In connection with their visit at either the orthopaedic or physiotherapy outpatient clinic, patients are invited to participate in the study. Patients consenting to participate will undergo knee joint laxity tests with both the Rolimeter and the Lachmeter, and in addition health-related and demographic data are collected.

The two tests are performed in random order for each patient, and the same physiotherapist conducts the two tests in each individual patient. The physiotherapist performing the two tests reads and notes the score on the first test, while a different physiotherapist, blinded to the score of the first test, reads and notes the score on the second test.

Agreement between the two scores are investigated using a Bland-Altman plot, with calculation of bias and upper and lower limits of agreements with 95% CIs. A priori, an acceptable difference between the two methods is set at 1 millimeter.

02

Conditions studied

  • Anterior Cruciate Ligament Injuries
  • Laxity of Ligament
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients are recruited consecutively from either the orthopaedic outpatient clinic (patients with ACL-injury) or the physiotherapy outpatient clinic (patients who have previously undergone ACL surgery) at Aarhus University Hospital.

Inclusion criteria

  • Patients with ACL injury awaiting potential ACL-surgery
  • Patients with previous ACL-surgery

Exclusion criteria

Exclusion Criteria:

  • Multiligament injury
  • PCL injury
04

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
60 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients with ACL injuries

    Patients who have sustained an ACL injury, surgically or non-surgically treated.

    Diagnostic Test: Knee joint laxity test

Interventions

  • Diagnostic testKnee joint laxity test

    Patients seen in an outpatient clinic in connection with an ACL injury or in connection with short or long-term follow-up after ACL surgery, will undergo a clinical assessment of their knee injury as part of standard care. This includes an assessment of knee joint laxity using both the Rolimeter and the Lachmeter, to allow for an assessment of agreement between the two methods.

    Also known as: Rolimeter, Lachmeter

05

What researchers measure

Primary outcomes

  1. Knee joint laxity (millimeters)

    Measurement of knee joint laxity using both a Rolimeter and a Lachmeter is conducted in connection with the patients' visit at the outpatient clinic.

    Time frame: For surgicaly treated patients: Between 1 year and up to 5 years post-surgery. For non-surgically treated patients: Up to 12 weeks after ACL injury.

06

Study locations

1 of 1 sites recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05614297
Lead sponsor
Region MidtJylland Denmark
Responsible party
Nanna Rolving (Senior researcher, Aarhus University Hospital) — Principal investigator
First posted
Nov 14, 2022
Start date
Sep 1, 2022
Primary completion
Mar 31, 2023 (estimated)
Completion
Mar 31, 2023 (estimated)
Last update
Nov 14, 2022

Study contacts

Nanna Rolving, PhD
Contact
Nanna.Rolving@rm.dk
0045 21289188
Torsten G Nielsen, MHSc
Contact
Torsten.Groenbech.Nielsen@auh.rm.dk
Nanna Rolving, PhD
principal investigator · Aarhus University Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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