View Clinical Trial (Medical Research Study)
Bone Physiology & Mechanics in Osteomyoplasty Amputation Rehabilitation - NCT00271362-73104(Clinical Trial 135302)
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| City: |
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Oklahoma City |
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State:
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OK |
| Zip Code: |
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73104 |
| Conditions: |
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Amputation - Fracture - Inflammation - Osteoporosis |
| Purpose: |
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The purpose of the study is to compare the effect of different lower limb amputation
surgical procedures on leg bone integrity and rehabilitation outcome.
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| Study summary: |
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Osteoporosis leading to increased risk of fracture, especially in the ipsilateral limb, is
well documented in lower limb amputees. The purpose of this research is to examine the
clinical utility of two amputation surgical procedures in: a) minimizing short and
longer-term deleterious effects of amputation on bone integrity relative to the antecedents
of osteoporotic change: reduced weight bearing capacity, inflammation, impaired muscle
viability, and vascular compromise, and b) deriving benefit from prosthetic rehabilitation
and exercise interventions.
In a randomized controlled clinical trial, we will test the hypotheses: In lower limb
traumatic and dysvascular amputation, when compared to the transtibial long posterior flap
amputation technique and the transfemoral Gottschalk method, the osteomyoplastic
reconstruction technique developed by Ertl:
1. Hypothesis 1: results in fewer detrimental effects on bone metabolism, structure, and
mass.
2. Hypothesis 2: leads to optimal rehabilitation and functional outcomes. Specifically, we
will examine, in traumatic and dysvascular lower limb amputees randomly assigned to
undergo either the long posterior flap amputation method or amputation with
osteomyoplastic reconstruction in transtibial amputation and either the Gottschalk
amputation method or amputation with osteomyoplastic reconstruction in transfemoral
amputation, differences in the following parameters at baseline, 6 weeks
(post-operative recuperation), and 6 months (termination of supervised rehabilitation
and exercise intervention).
We will assess bone integrity in patients undergoing standard amputation versus
osteomyoplastic reconstruction by measuring bone metabolism and bone mineral density and
mineral content. Second, we will measure inflammatory response in patients undergoing
standard amputation versus osteomyoplastic reconstruction by assessing weight bearing and
impact, muscle integrity, and limb vascularity. Last, we will compare rehabilitation and
functional outcome in patients undergoing standard amputation versus osteomyoplastic
reconstruction by assessing prosthetic mobility, functional capacity, activity levels, and
quality of life. |
| Criteria: |
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Inclusion Criteria:
Adult lower limb PVD-related or traumatic amputees who are appropriate candidates for
amputation rehabilitation exercise.
Exclusion Criteria:
1. Cognitive dysfunction (MiniMental scores <23), advanced neuropathies, or neurological
impairment (CVA, Parkinson's) with residual loss of function enough to preclude
exercise;
2. Unresolved MI (high isoenzymes), angina, arrhythmia, 3rd degree AV block, fixed-rate
pacer;
3. Recent embolus/thrombophlebitis, myocarditis, pericarditis, or cardiomyopathy;
4. Resting SBP >200mmHg or DBP >100mmHg;
5. Uncontrolled metabolic disease, liver or kidney failure, alcohol/drug addiction;
acute infection;
6. Exercise-exacerbated neuromuscular/musculoskeletal disorders; irreducible hip/leg
contractures. |
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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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October 22, 2010 |
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