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Comfort of GraduCheck Under Compression Bandaging

NCT05160792 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2021-12-16

No results posted yet for this study

Summary

The purpose of this service evaluation is to evaluate the comfort in use of GraduCheck® by volunteers, under standard compression bandages.

Conditions

  • Compression Bandage

Interventions

DEVICE

Pressure monitoring system under compression bandages on index leg

Adding a Graducheck device under the compression bandages on the index leg and comparing to other leg, which has compression but without the device.

Sponsors & Collaborators

  • Veinsense Ltd

    collaborator UNKNOWN

  • The Whiteley Clinic

    lead OTHER

Principal Investigators

  • Mark S Whiteley, MS · The Whiteley Clinic Ltd

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-31
Primary Completion
2022-03-31
Completion
2022-03-31

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05160792 on ClinicalTrials.gov