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Accommodating for Residual Limb Fluid Volume Change

NCT ID: NCT02124876

Last Updated: 2020-11-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

45 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-06-30

Study Completion Date

2014-06-06

Brief Summary

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The purpose of this study is to quantify residual limb fluid volume changes between morning and afternoon hours, and to determine if fluid volume change is correlated with activity.

Detailed Description

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Conditions

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Diurnal Residual Limb Fluid Volume Fluctuation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Transtibial amputees

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* transtibial amputation
* at least 18 months after amputation surgery
* ability to walk on a treadmill and stand for 90 seconds

Exclusion Criteria

* skin breakdown on the residual limb
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NIH

Sponsor Role collaborator

University of Washington

OTHER

Sponsor Role lead

Responsible Party

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Joan Sanders

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Washington

Seattle, Washington, United States

Site Status

Countries

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United States

Other Identifiers

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R01HD060585

Identifier Type: NIH

Identifier Source: secondary_id

View Link

STUDY00002557

Identifier Type: -

Identifier Source: org_study_id