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Clinical Trial Summary

Port Wound Closure compares synthetic tissue adhesives with seam for cutaneous wound closure to port plant in terms of cosmetic results and time savings at comparable risk for wound infection.


Clinical Trial Description

Study patients who undergo a subcutaneous venous port implant procedure are randomized into control group (conventional sutures) or into interventional group (synthetic tissue adhesive). The intervention time is documented. Follow-up visit is performed 8 weeks after port implantation. It includes a photo documentation, quality of life questionnaire (EQ5D) and pain scala questionnaire (POSAS) by patient and by 3 independent observers as well as the documentation of complications. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02551510
Study type Interventional
Source Jena University Hospital
Contact
Status Completed
Phase N/A
Start date August 2015
Completion date May 2019