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Bone Physiology & Mechanics in Osteomyoplasty Amputation Rehabilitation

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VA Office of Research and Development

Status

Terminated

Conditions

Osteoporosis
Inflammation
Fracture
Amputation

Treatments

Procedure: Osteomyoplasty vs. routine long posterior flap
Behavioral: Amputation rehabilitation exercise program

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT00271362
O3789-I

Details and patient eligibility

About

The purpose of the study is to compare the effect of different lower limb amputation surgical procedures on leg bone integrity and rehabilitation outcome.

Full description

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.

Enrollment

95 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

95 participants in 1 patient group

1
Active Comparator group
Description:
comparing 2 surgical procedures
Treatment:
Procedure: Osteomyoplasty vs. routine long posterior flap
Behavioral: Amputation rehabilitation exercise program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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