MedTrace Logo

Compression Device Safety Study

NCT00732823 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2008-10-31

No results posted yet for this study

Summary

To evaluate the safety of the Compression Device to subjects with venous insufficiency and oedema.

Conditions

  • Venous Insufficiency

Interventions

DEVICE

Placebo - No device worn

DEVICE

Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs

DEVICE

Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs

DEVICE

Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs

Sponsors & Collaborators

Principal Investigators

  • wolfgang Vanscheidt · Facharzt für Dermatologie Phlebologie Allergologie

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2005-10-31
Completion
2005-10-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Companies

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 NCT00732823 on ClinicalTrials.gov