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Compression Device Safety Study on Edema

NCT00732719 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2008-10-31

No results posted yet for this study

Summary

To evaluate the safety of the prototype Compression Device in subjects with Oedema

Conditions

Interventions

DEVICE

Prototype device (unnamed) worn-no pressure given (placebo) from inflatable cuffs

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

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 · Hautarzt Phlebologe Allergologe

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-10-31
Primary Completion
2004-11-30
Completion
2004-12-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases
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 NCT00732719 on ClinicalTrials.gov