Expired Study
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Lebanon, New Hampshire 03756


Purpose:

The purpose of this study is to evaluate and compare the clinical, radiographic (x-ray) and cost effectiveness outcomes (cost relative to risks and benefits) of two different minimally invasive knee joint replacement surgical techniques. The primary study hypothesis is that in comparing total knee replacement performed with the two different surgical techniques that respect four minimally invasive surgery principles (low-profile instrumentation, "minimally invasive" incision, overall minimal knee surgical intervention), a faster return to function will result when the technique does not incise the tendon.


Study summary:

This study does not include financial compensation for treatments involved.


Criteria:

Inclusion Criteria: - Presence of severely symptomatic knee osteoarthritis that has failed non- operative treatment - Males and non-pregnant females, 35-85 years of age at the time of surgery - ASA class 1 or 2 - Procedure will not require computer navigation - Patient/Surgeon has not requested another implant - Patient has signed an IRB approved study consent form - Patient is able and willing to actively participate in post-operative rehabilitation program - Patient understands study requirements - Patient is willing to comply with follow-up visits and diary documentations - Patient is capable of independent ambulation Exclusion Criteria: - Skeletal immaturity - More than 10 degrees of valgus or varus deformity as measured from a weight bearing AP alignment view - Patients with bilateral knee osteoarthritis who are considering a simultaneous bilateral procedure - Bone or ligament insufficiency that requires the use of augments or stems, or constrained component - Daily pre-operative use of narcotic pain medication - Prior knee arthroplasty - Patient is a prisoner - Patient has had prior tibial tubercle osteotomy - Patient's surgical knee would require removal of hardware prior to TKA - Patient has < 95 degrees flexion pre-operatively


NCT ID:

NCT00633113


Primary Contact:

Principal Investigator
Ivan M Tomek, MD
Dartmouth-Hitchcock Medical Center


Backup Contact:

N/A


Location Contact:

Lebanon, New Hampshire 03756
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 16, 2018

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