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Bone Physiology & Mechanics in Osteomyoplasty Amputation Rehabilitation

Primary Purpose

Amputation, Fracture, Inflammation

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Amputation rehabilitation exercise program
Osteomyoplasty vs. routine long posterior flap
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Amputation focused on measuring Exercise, Physical function, Prosthetic mobility, Rehabilitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Adult lower limb PVD-related or traumatic amputees who are appropriate candidates for amputation rehabilitation exercise. Exclusion Criteria: Cognitive dysfunction (MiniMental scores <23), advanced neuropathies, or neurological impairment (CVA, Parkinson's) with residual loss of function enough to preclude exercise; Unresolved MI (high isoenzymes), angina, arrhythmia, 3rd degree AV block, fixed-rate pacer; Recent embolus/thrombophlebitis, myocarditis, pericarditis, or cardiomyopathy; Resting SBP >200mmHg or DBP >100mmHg; Uncontrolled metabolic disease, liver or kidney failure, alcohol/drug addiction; acute infection; Exercise-exacerbated neuromuscular/musculoskeletal disorders; irreducible hip/leg contractures.

Sites / Locations

  • VA Medical Center, Oklahoma City

Arms of the Study

Arm 1

Arm Type

Active Comparator

Arm Label

1

Arm Description

comparing 2 surgical procedures

Outcomes

Primary Outcome Measures

Bone Integrity

Secondary Outcome Measures

Inflammatory Response

Full Information

First Posted
December 28, 2005
Last Updated
April 19, 2017
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT00271362
Brief Title
Bone Physiology & Mechanics in Osteomyoplasty Amputation Rehabilitation
Official Title
Bone Physiology & Mechanics in Osteomyoplasty Amputation Rehabilitation
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Terminated
Why Stopped
This project is no longer active with DVA.
Study Start Date
January 2006 (Actual)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to compare the effect of different lower limb amputation surgical procedures on leg bone integrity and rehabilitation outcome.
Detailed 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: Hypothesis 1: results in fewer detrimental effects on bone metabolism, structure, and mass. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amputation, Fracture, Inflammation, Osteoporosis
Keywords
Exercise, Physical function, Prosthetic mobility, Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
95 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
comparing 2 surgical procedures
Intervention Type
Behavioral
Intervention Name(s)
Amputation rehabilitation exercise program
Intervention Description
participants will be physically exercised with a full array of exercise methodologies.
Intervention Type
Procedure
Intervention Name(s)
Osteomyoplasty vs. routine long posterior flap
Intervention Description
participants enrolled randomly in one of two surgical procedures.
Primary Outcome Measure Information:
Title
Bone Integrity
Time Frame
6 weeks - 6 months
Secondary Outcome Measure Information:
Title
Inflammatory Response
Time Frame
6 weeks - 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult lower limb PVD-related or traumatic amputees who are appropriate candidates for amputation rehabilitation exercise. Exclusion Criteria: Cognitive dysfunction (MiniMental scores <23), advanced neuropathies, or neurological impairment (CVA, Parkinson's) with residual loss of function enough to preclude exercise; Unresolved MI (high isoenzymes), angina, arrhythmia, 3rd degree AV block, fixed-rate pacer; Recent embolus/thrombophlebitis, myocarditis, pericarditis, or cardiomyopathy; Resting SBP >200mmHg or DBP >100mmHg; Uncontrolled metabolic disease, liver or kidney failure, alcohol/drug addiction; acute infection; Exercise-exacerbated neuromuscular/musculoskeletal disorders; irreducible hip/leg contractures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel J. Brackett, MD
Organizational Affiliation
VA Medical Center, Oklahoma City
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Medical Center, Oklahoma City
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States

12. IPD Sharing Statement

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Bone Physiology & Mechanics in Osteomyoplasty Amputation Rehabilitation

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