NCT01950208

Brief Summary

the purpose of this study is to develop and validate a new PRO measurement tool for the knee joint, the so-called Munich Knee Questionnaire (MKQ), allowing for a qualitative self-assessment of the Knee Injury and Osteoarthritis Outcome Score (KOOS), the International Knee Documentation Committee (IKDC), the Lysholm Knee Score, the Western Ontario Meniscal Evaluation Tool (WOMET) and the Tegner Score.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
105

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2012

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

August 1, 2012

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2012

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2013

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

September 15, 2013

Completed
10 days until next milestone

First Posted

Study publicly available on registry

September 25, 2013

Completed
Last Updated

September 25, 2013

Status Verified

September 1, 2013

Enrollment Period

2 months

First QC Date

September 15, 2013

Last Update Submit

September 20, 2013

Conditions

Knee Injury

Keywords

Assessment

Outcome Measures

Primary Outcomes (1)

  • Munich Knee Questionnaire (MKQ)

    up to 6 weeks starting from onset of symptoms

Secondary Outcomes (1)

  • The self-assessment of the Knee Injury and Osteoarthritis Outcome Score (KOOS)

    up to 6 weeks starting from onset of symptoms

Other Outcomes (1)

  • The International Knee Documentation Committee (IKDC)

    up to 6 weeks starting from onset of symptoms

Study Arms (1)

knee pain

patients suffering from knee injury

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

all patients with knee pain

You may qualify if:

  • all patients presenting with knee pain

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Klinik und Poliklinik für Unfallchirurgie

Munich, Bavaria, 81675, Germany

Location

Related Links

MeSH Terms

Conditions

Knee Injuries

Condition Hierarchy (Ancestors)

Leg InjuriesWounds and Injuries

Study Officials

  • Chlodwig Kirchhoff, MD

    Technical University of Munich

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PD Dr. med.

Study Record Dates

First Submitted

September 15, 2013

First Posted

September 25, 2013

Study Start

August 1, 2012

Primary Completion

October 1, 2012

Study Completion

April 1, 2013

Last Updated

September 25, 2013

Record last verified: 2013-09

Locations

DE(1)