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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02578589
Other study ID # 280981PM
Secondary ID
Status Recruiting
Phase N/A
First received October 11, 2015
Last updated October 6, 2017
Start date September 2014
Est. completion date December 2020

Study information

Verified date October 2017
Source Regionshospitalet Silkeborg
Contact Steffen Sauer, MD
Phone 004531560149
Email sauer_steven@web.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this trial is to evaluate the effect of conservative treatment in comparison to arthroscopic resection of pathological medial plicae of the knee for patients with medial plica syndrome. The investigators expect conservative treatment to be significantly superior to arthroscopic plica resection with regard to symptom remission and return to prior functional level.


Recruitment information / eligibility

Status Recruiting
Enrollment 72
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Aged over 18 years

- History of antermedial knee pain

- Palpable medial band in clinical examination or medial plica appearence on MRI

- Absence of all of the following diagnoses: Osteoarthritis, osteochondritis dissecans, meniscal injury, patella subluxation, pes anserinus bursit, patellofemoral pain syndrome

- Given declaration of consent

- Joining a fitness centre for the duration of minimum 3 months at their own expense.

Exclusion Criteria:

Aged under 18 years

- Presence of one or more of the following diagnoses: Osteoarthritis, osteochondritis dissecans, meniscal injury, patella subluxation, pes anserinus bursit, patellofemoral pain syndrome

- Prior surgical intervention, infection, fracture or patellar luxation concerning the relevant knee

- Not willing to join a fitness centre for the duration of minimum 3 months at their own expense

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Plica resection vs conservative treatment
Plica resection vs conservative treatment

Locations

Country Name City State
Denmark Regionshospital Silkeborg Silkeborg
Denmark Regionshospitalet Silkeborg Silkeborg

Sponsors (1)

Lead Sponsor Collaborator
Regionshospitalet Silkeborg

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lysholm-Scale (Units on a scale) Difference of minimum 5 points concerning the average scoring outcome on the Lysholm Knee Scoring Scala in favor of patients undergoing conservative treatment in comparison to patients undergoing arthroscopic plica resection at 2 year follow up. Units of measure (Units on a scale) 2 years
Secondary Kujala-Scale (Units on a scale) Secondary endpoints: Higher average scoring outcome on the Anterior Knee Pain Scala (Kujala) in favor of patients undergoing conservative treatment in comparison to patients undergoing arthroscopic plica resection at 2 year follow up. Lower average results on Visual Anologue Scale concerning knee pain while walking indicated by patients undergoing conservative treatment in comparison to patients undergoing arthroscopic plica resection at 2 year follow up. Units of measure (Units on a scale) 2 years
Secondary QOL-Scale (Units on a scale) Higher average scoring outcome on the Quality of Life Scala (extracted from KOOS) in favor of patients undergoing conservative treatment in comparison to patients undergoing arthroscopic plica resection at 2 year follow up. Units of measure (Units on a scale) 2 years
Secondary VAS-Scale (Visual Analog Scale for pain) (Units on a scale) Lower average results on Visual Anologue Scale concerning knee pain while walking indicated by patients undergoing conservative treatment in comparison to patients undergoing arthroscopic plica resection at 2 year follow up. Units of measure (Units on a scale) 2 years