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ACTIVE NOT RECRUITING
NCT07024342
NA

Optimizing Prosthetic Prescription to Mitigate the Effects of Perspiration

Sponsor: VA Puget Sound Health Care System

View on ClinicalTrials.gov

Summary

The specific aim of this research is to compare three clinically available liners, each intended to address problems of residual limb perspiration, with the as-prescribed liner of lower limb prosthesis user and determine their effect on stability, suspension, and comfort.

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

180

Start Date

2022-10-04

Completion Date

2026-09

Last Updated

2026-01-09

Healthy Volunteers

No

Interventions

DEVICE

Liner perforated with very small diameter holes

A commercially available, elastomeric liner perforated with very small holes (approximately 0.3 mm diameter) to allow perspiration to drain. This liner is worn between the skin and the participant's prosthetic socket.

DEVICE

Liner perforated with somewhat larger diameter holes

A commercially available, elastomeric liner perforated with somewhat larger holes (approximately 1.5 mm diameter) to allow perspiration to drain. This liner is worn between the skin and the participant's prosthetic socket.

DEVICE

Liner-liner

A thin, special purpose half-ply sock which may reduce the effects of perspiration. The liner-liner is worn between the skin and the participant's as-prescribed liner.

DEVICE

As-prescribed liner

A commercially available, elastomeric liner with no perforations. This liner is worn between the skin and the participant's prosthetic socket.

Locations (1)

VA Puget Sound Health Care System Seattle Division

Seattle, Washington, United States