View Clinical Trial (Medical Research Study)
In Vivo Arthroscopic Behavior of the Infrapatellar Plica of the Knee - NCT00643487-13202(Clinical Trial 211679)
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| City: |
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Syracuse |
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State:
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NY |
| Zip Code: |
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13202 |
| Conditions: |
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Patellofemoral Pain Syndrome |
| Purpose: |
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Anterior knee pain has been an enigmatic problem for orthopedic surgeons. Recent studies,
as well as the clinical observation of the principle investigator have suggested that
arthroscopic resection of the infrapatellar plica (IPP), a vestigial remnant from embryonic
development of no known clinical or biological significance, may eliminate this pain. The
mechanism whereby this pain is related to the IPP is unclear. This study will document the
mechanical behavior of the IPP as recorded on video among a group of subjects who are
undergoing arthroscopy. Radiographic verification of the observed behavior will be obtained
by injection of contrast material, and then fluoroscopic recording of a standard series of
motions. The plica will be resected to avoid any possibility of residual symptoms related
to its presence, a further fluoroscopy of the knee without plical attachment, and the
procedure terminated.
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| Study summary: |
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The infrapatellar plica (IPP) of the human knee is vestigial remnant of the embryologic
division between the medial and lateral compartments of the knee, present in 85.5% of
knees1, felt by some to be of no clinical significance other than acting as a block to
visualization an movement during arthroscopy.2 S.J. Kim 3,4, T.V. Smallman (clinical
observation), and C.R. Boyd 5 have documented knee pain presenting in association with
infrapatellar plicae. This study seeks to assess the relationship between knee motion,
activation of the extensor apparatus, and the IPP. The hypothesis to be evaluated is:
the infrapatellar plica is a structure of fundamental biomechanical significance, allowing
the transmission of force from the extensor apparatus to the distal femur through the fat
pad, and acting as a restraint and a modulator of fad pad mobility.
Subjects will be identified by the PI at their office visit. The subject will be consented.
The consent will be discussed and verified in a second office visit before surgery. The
subject will undergo arthroscopy specifically directed toward identifying and treating known
pathology. Once this is finished, if an IPP is present, it will be injected with
radiographic contrast material. A series of maneuvers will be performed involving passive
and active motion of the knee and active contraction of the quadriceps apparatus. Videotape
recording and fluoroscopy will be undertaken. The plica will be removed. Another
fluoroscopy will be performed. The patient will be followed according to the standard
practice for arthroscopy and the defined pathology. |
| Criteria: |
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Inclusion:
- Healthy subject
- >18 years of age, skeletally mature
- Pending knee joint arthroscopy.
Exclusion:
- Active infection |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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August 3, 2010 |
Modifications to
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