The Influence of Compression Stockings on Skin's Barrier Function at Patients With Chronic Venous Disease
This study has been completed.
Sponsor:
University Medicine Greifswald
Collaborator:
Bauerfeind AG, Zeulenroda, Germany
Information provided by:
University Medicine Greifswald
ClinicalTrials.gov Identifier:
NCT00196443
First received: September 12, 2005
Last updated: NA
Last verified: September 2005
History: No changes posted
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The purpose of this study is to investigate if wearing of compression stockings influences the skin moisture. Conservative stockings are compared with urea containing compression stockings to find out if using urea prevents dehydration of the skin while wearing the urea compression stockings. Secondary aim was to find out if urea containing stockings increase the compliance to wear the compression stockings regulary by patients with diagnosed chronic venous insufficiency.
Condition | Intervention | Phase |
---|---|---|
Venous Insufficiency |
Device: urea contained compressing stockings Device: compressing stockings |
Phase 2 Phase 3 |
Study Type: | Interventional |
Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind Primary Purpose: Treatment |
Official Title: | Prospective, Randomized and Explorative Controlled Study About Influences of Compression Stockings on Skin's Barrier Function at Patients With Chronic Venous Insufficiency |
Further study details as provided by University Medicine Greifswald:
Primary Outcome Measures:
- skin moisture at day 0 and day 7
- loss of water throughout epidermis at day 0 and day 7
- throatiness of epidermis at day 0 and day 7
Secondary Outcome Measures:
- compliance of patients at every day of intervention
Estimated Enrollment: | 42 |
Study Start Date: | June 2005 |
Estimated Study Completion Date: | July 2005 |
Eligibility
Ages Eligible for Study: | 18 Years to 80 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Clincial diagnosis of chronic venous insufficiency
- Age: 18-80 years
- Patient's information and willingness to participate
Exclusion Criteria:
- Age under 18 years
- Lower limp edema not caused by venous insufficiency
- Acute deep venous thrombosis
- Arterial occlusive disease
- Diabetes mellitus with neuropathy or peripheral arterial disturbance of perfusion
- immobile Patients
- Pregnancy
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00196443
Locations
Germany | |
Clinic and Polyclinic of Dermatology, Ernst-Moritz-Arndt-University of Greifswald | |
Greifswald, Fleischmannstr. 42-44, Germany, 17475 |
Sponsors and Collaborators
University Medicine Greifswald
Bauerfeind AG, Zeulenroda, Germany
Investigators
Principal Investigator: | Michael Jünger, Prof. Dr. | Clinic and Polyclinic of Dermatology, University of Greifswald |
Study Chair: | Andrea Ladwig | Clinic and Polyclinic of Dermatology, University of Greifswald |
More Information
No publications provided
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on October 16, 2012
No publications provided
ClinicalTrials.gov Identifier: | NCT00196443 History of Changes |
Other Study ID Numbers: | Bau-Phleb-17032005 |
Study First Received: | September 12, 2005 |
Last Updated: | September 12, 2005 |
Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
Additional relevant MeSH terms:
Venous Insufficiency Vascular Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on October 16, 2012