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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01504100
Other study ID # 201103111RC
Secondary ID
Status Completed
Phase N/A
First received July 1, 2011
Last updated October 29, 2013
Start date May 2011
Est. completion date October 2013

Study information

Verified date October 2013
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

Patellar subluxation is a common disorder that may cause patellofemoral pain syndrome. The efficiency of patellar taping in the treatment of patellofemoral pain syndrome has been reported good outcomes in most patients. However, some studies reported less effective in patients with higher body mass index, larger lateral patellofemoral angle, and smaller Q angle. The investigators hypothesized that femoral internal rotation is a negative factor to the patellar taping. The investigators enroll consecutive 100 patients with anterior knee pain and radiographic evidence of patellar subluxation. The investigators determine femoral rotation via physical examination. The visual analogue scale was evaluate to compare the result between the those with and without femoral internal rotation.


Description:

Consecutive 100 patients with anterior knee pain and compatible with inclusion criteria. Before treatment, an independent physiotherapist evaluates whether femoral internal rotation or not via physical therapy, and another studying nurse records the visual analog scale and measures Q angle. After evaluation, McConnell taping is applied to these patients. Two weeks later, outcomes are recorded including visual analog scale, satisfactory, and complication. The outcomes are compared between those with and without femoral internal rotation.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date October 2013
Est. primary completion date October 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- anterior knee pain

- radiographic evidence of patellar subluxation

Exclusion Criteria:

- history of patellar dislocation

- osteoarthritis of ipsilateral knee

- pregnancy

- history of knee injury

- BMI > 35

- allergy to taping

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
Taiwan Department of Orthopaedic Surgery, National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knee pain The visual analog scale are measured before and two weeks after taping. two weeks No
Secondary Satisfactory The patients recorded the satisfactory score by theyself from 0 to 10. Ten degree means most satisfactory. 2 weeks No
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