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Study to Evaluate the Effect of Sorbion Sachet S Wound Dressing

NCT01319097 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2011-09-08

No results posted yet for this study

Summary

This is a clinical study to evaluate the effects of sorbion sachet s wound dressing on soft tissue edema and wound bioburden in moderately to highly exuding pressure ulcers.

Conditions

  • Pressure Ulcers

Interventions

OTHER

Sorbion Sachet S

Dressing is indicated for moderately to heavily exuding wounds.

Sponsors & Collaborators

  • Sorbion Aktiengesellschaft, Germany

    collaborator UNKNOWN

  • Southwest Regional Wound Care Center

    lead OTHER

Principal Investigators

  • Randall D Wolcott, M.D. · Southwest Regional Wound Care Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2011-08-31
Completion
2011-08-31

Countries

  • United States

Study Locations

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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 NCT01319097 on ClinicalTrials.gov