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Clinical Trials/NCT02124876
NCT02124876
Completed
Not Applicable

Accommodating for Residual Limb Fluid Volume Change

University of Washington1 site in 1 country45 target enrollmentJune 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diurnal Residual Limb Fluid Volume Fluctuation
Sponsor
University of Washington
Enrollment
45
Locations
1
Primary Endpoint
Residual limb fluid volume
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
June 6, 2014
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Joan Sanders

Professor

University of Washington

Eligibility Criteria

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

Outcomes

Primary Outcomes

Residual limb fluid volume

Time Frame: 1 day

Secondary Outcomes

  • Duration of walking and moving(1 day)

Study Sites (1)

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