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Low Magnitude Mechanical Stimuli Effects on Bone Structure in ESRD

Primary Purpose

Renal Osteodystrophy

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Low magnitude mechanical stimuli
Sponsored by
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Osteodystrophy focused on measuring Renal Osteodystrophy

Eligibility Criteria

21 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: ages 21-65 years Maintenance Hemodialysis Exclusion Criteria: Active Malignancy History of myocardial infarction Congestive heart failure III-IV stage Cerebrovascular disease Planned relocation Pregnancy Anticipated living-donor transplantation within the coming 6 months Liver failure Neuropathies Prior lower extremity amputation or difficult with ambulation History of hip fracture History of hip replacement History of orthostatic hypotension or a balance disorder History of a fall within 6 months prior to enrollment Difficulty in ambulation will be defined as difficulty climbing two flights of stairs or walking three blocks Patients with pacemaker or other metal implants that are contraindicated for MRI scans Weight > 113kg HIV Positive

Sites / Locations

  • Childen's Hospital of Philadelphia

Outcomes

Primary Outcome Measures

Trabecular Microarchitecture

Secondary Outcome Measures

Full Information

First Posted
August 14, 2006
Last Updated
April 13, 2015
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT00364234
Brief Title
Low Magnitude Mechanical Stimuli Effects on Bone Structure in ESRD
Official Title
Low Magnitute Mechanical Stimuli Effects on Bone Structure in ESRD
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
September 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The proposed 6 month pilot and feasibility randomized trial will evaluate LMMS as an anabolic stimulus to bone in 30 adults on maintenance hemodialysis. The intervention will consist of 20 minute daily sessions in the home standing on an active LMMS platform or a placebo device that emits an audible hum suggestive of an active device. Each device contains an electronic monitor that documents adherence. The study will examine trabecular bone volume fraction (bone volume/total volume, BV/TV %) and architecture using microMRI, and cortical volumetric BMD and dimensions using QCT at baseline and 6 months. The hypothesis is that active LMMS will results in greater mean changes in trabecular and cortical parameters in hemodialysis patients. The proposed study will test the feasibility of conducting the intervention in dialysis patients and will generate preliminary data on rates of change in trabecular and cortical parameters in the active and placebo groups.
Detailed Description
Renal osteodystrophy (ROD) is a multifactorial and pervasive disorder in chronic kidney disease (CKD). As renal failure progresses, ensuing abnormal parathyroid hormone (PTH) secretion and mineral metabolism result in sclerosis of trabecular bone, thinning of cortical bone, and increased cortical porosity.(1) Despite the widespread use of phosphate binders and vitamin D therapies, hip fracture rates and mortality risk following fractures are markedly greater in dialysis patients, compared with the general population. The vast majority of studies of bone loss in CKD relied on dual energy x-ray absorptiometry (DXA) measures of bone mineral density (BMD). However, DXA summarizes the total bone mass within the projected bone area, concealing disease effects on trabecular and cortical bone. For example, in high-turnover ROD, increased trabecular volume may offset cortical bone loss, resulting in normal or increased areal-BMD despite poor bone strength. Quantitative computed tomography (QCT) enables discrete assessment of trabecular and cortical volumetric BMD and dimensions. However, this is an incomplete solution in the setting of CKD because QCT does not assess trabecular architecture. Micro-magnetic resonance imaging (µMRI) provides a non-invasive technique to assess trabecular architecture. The µMRI data are quantified by 3D digital processing methods, such as topological analysis, to determine trabecular properties. Our pilot study of µMRI in dialysis patients revealed significant reductions in cortical thickness and suggested deterioration in the trabecular network. This innovative imaging modality may be uniquely suited to the assessment of ROD therapies. Mechanical forces on the skeleton arise from muscle contraction and these forces generate signals that modulate bone architecture. Animal studies demonstrated that daily exposure to low magnitude mechanical stimuli (LMMS) enhanced trabecular and cortical bone quantity and quality. A randomized trial of LMMS in post-menopausal women demonstrated that LMMS were associated with increased DXA BMD, without adverse effects. LMMS may be uniquely suited to restore cortical and trabecular bone structure in ROD. The study will enroll adults, ages 21-65 years, treated with maintenance hemodialysis at UPENN. The study will exclude the elderly and subjects with major co-morbid conditions in order to increase the likelihood that subjects will complete the 6 month intervention without significant interruptions due to hospitalization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Osteodystrophy
Keywords
Renal Osteodystrophy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Low magnitude mechanical stimuli
Intervention Description
20 minutes standing on low magnitude high frequency vibrating platform
Primary Outcome Measure Information:
Title
Trabecular Microarchitecture
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ages 21-65 years Maintenance Hemodialysis Exclusion Criteria: Active Malignancy History of myocardial infarction Congestive heart failure III-IV stage Cerebrovascular disease Planned relocation Pregnancy Anticipated living-donor transplantation within the coming 6 months Liver failure Neuropathies Prior lower extremity amputation or difficult with ambulation History of hip fracture History of hip replacement History of orthostatic hypotension or a balance disorder History of a fall within 6 months prior to enrollment Difficulty in ambulation will be defined as difficulty climbing two flights of stairs or walking three blocks Patients with pacemaker or other metal implants that are contraindicated for MRI scans Weight > 113kg HIV Positive
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary B Leonard, MD, MSCE
Organizational Affiliation
Children's Hospital of Philadelphia , Philadelphia, Pennsylvania, United States
Official's Role
Principal Investigator
Facility Information:
Facility Name
Childen's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

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Low Magnitude Mechanical Stimuli Effects on Bone Structure in ESRD

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