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Morphology of the VMO in Patients With PFPS and Healthy Young Adults--A Sonographic Study

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2005 by National Taiwan University Hospital.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT00173147
First received: September 12, 2005
Last updated: October 24, 2008
Last verified: April 2005
  Purpose

Background:Patellofemoral pain syndrome(PFPS) is a common knee disorder characterized by anterior or retropatellar pain associated with activities that load the patellofemoral joint. Previous studies reveal that the vastus medialis obliquus(VMO) is an important dynamic medial stabilizer of the patellar. Insufficiency of the VMO leads to lateral shift of the patella and the increases the patellofemoral contact force. An in vitro study conducted by Hubbard JK. et al. claimed that there were no significant relationship between several morphologic characteristics of the VMO and the extent of patellofemoral joint deterioration. We consider that the condition might be different in vivo, so we chose ultrasonogrphy as the measurement tool to examine the morphology of the VMO in PFPS patients and healthy controls. Purpose:To determine if there are significant differences in several morphologic parameters of the VMO between patients with PFPS and healthy controls under 50. Method:31 PFPS patients and 31 matched healthy adults under 50 were recruited for the study. The HDI 5000 ultrasonography machine was used to evaluate morphologic parameters of the VMO, including the percent of patella attachment, fiber angle, the volume attached to the patella, and the change of shape of the VMO.


Condition
Patellofemoral Pain Syndrome

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Morphology of the Vastus Medialis Obliquus in Patients With Patellofemoral Pain Syndrome and Healthy Young Adults --A Sonographic Study

Further study details as provided by National Taiwan University Hospital:

Study Start Date: May 2005
  Eligibility

Ages Eligible for Study:   15 Years to 50 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. under 50 years old.
  2. Have a diagnosis of PFPS.

Exclusion Criteria:

  1. Diagnosis other than PFPS,such as meniscal lesion, ligamentous instability ,patellar tendon pathology, traction apophysitis, radiation pain, referred pain, ect.
  2. Knee operation within three month.
  3. X-ray findings (1)joint space narrowing (2)osteophyte formation
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00173147

Locations
Taiwan
NTUH Recruiting
Taipei, Taiwan, 100
Contact: Hsin-Yu Mao, Master    02-23123456 ext 7556    babymmeeww@yahoo.com.tw   
Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Study Chair: Mei-Hwa Jan, Master NTU department of physical therapy
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00173147     History of Changes
Other Study ID Numbers: 9461700502
Study First Received: September 12, 2005
Last Updated: October 24, 2008
Health Authority: Taiwan: Department of Health

Additional relevant MeSH terms:
Patellofemoral Pain Syndrome
Syndrome
Disease
Joint Diseases
Musculoskeletal Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on November 20, 2014