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OpenTrials
Completed

NCT Number: NCT02124876

Accommodating for Residual Limb Fluid Volume Change

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.

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Key information

Conditions

Diurnal Residual Limb Fluid Volume Fluctuation

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Washington

Seattle, Washington, 98075, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Residual limb fluid volume

    Time frame: 1 day

Secondary outcomes

  1. Duration of walking and moving

    Time frame: 1 day

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Collaborators

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

Registry information

Acronym: AM-PM

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Apr 28, 2014
Registry last updated
Nov 4, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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