NCT03608189

Brief Summary

The purpose of this study is to assess ACL injury and other pathological knee conditions from the combination of signals that are known to provide information on the knee joint.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Aug 2018

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 23, 2018

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 31, 2018

Completed
1 day until next milestone

Study Start

First participant enrolled

August 1, 2018

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2018

Completed
Last Updated

July 31, 2018

Status Verified

July 1, 2018

Enrollment Period

5 months

First QC Date

July 23, 2018

Last Update Submit

July 23, 2018

Conditions

ACL Injury

Keywords

OsteoarthritisACL injuryKnee traumaMeniscus tear

Outcome Measures

Primary Outcomes (1)

  • Objective evaluation method for knee disorder recovery

    ACL injury recovery (confirmed by using MRI)

    Six months

Study Arms (1)

ACL injury subjects

Subjects with anterior cruciate ligament injuries.

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Patient participating in rehabilitation due to ACL injuries and potential other knee disorders.

You may qualify if:

  • ACL injury
  • Ages 18-40
  • Female

You may not qualify if:

  • BMI under 18
  • BMI over 40
  • Contraindications to MRI

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Oulu

Oulu, North Ostrobothnia, 90014, Finland

Location

MeSH Terms

Conditions

Anterior Cruciate Ligament InjuriesOsteoarthritis

Condition Hierarchy (Ancestors)

Knee InjuriesLeg InjuriesWounds and InjuriesArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Study Officials

  • Simo Saarakkala, Ph.D.

    University of Oulu

    PRINCIPAL INVESTIGATOR

  • Osmo Tervonen, Ph.D., M.D.

    Oulu University Hospital

    STUDY DIRECTOR

Central Study Contacts

Jérôme Thevenot, PhD

CONTACT

+358 294 48 6004jerome.thevenot@oulu.fi

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 23, 2018

First Posted

July 31, 2018

Study Start

August 1, 2018

Primary Completion

December 31, 2018

Study Completion

December 31, 2018

Last Updated

July 31, 2018

Record last verified: 2018-07

Locations

FI(1)