Fixation of Skin Grafts in Patients With Burns: Comparison Between Cyanoacrylate Glue and Skin Staples
Tracking Information | |||||
---|---|---|---|---|---|
First Received Date ICMJE | August 10, 2006 | ||||
Last Updated Date | August 10, 2006 | ||||
Start Date ICMJE | January 2002 | ||||
Primary Completion Date | |||||
Current Primary Outcome Measures ICMJE | |||||
Original Primary Outcome Measures ICMJE | |||||
Change History | No Changes Posted | ||||
Current Secondary Outcome Measures ICMJE | |||||
Original Secondary Outcome Measures ICMJE | |||||
Current Other Outcome Measures ICMJE | |||||
Original Other Outcome Measures ICMJE | |||||
Descriptive Information | |||||
Brief Title ICMJE | Fixation of Skin Grafts in Patients With Burns: Comparison Between Cyanoacrylate Glue and Skin Staples | ||||
Official Title ICMJE | Fixation of Skin Grafts in Patients With Burns: Comparison Between Cyanoacrylate Glue and Skin Staples | ||||
Brief Summary | Skin graft fixation is essential for the success of its survival. There are several common methods for skin graft fixation including sutures, skin staples and glue. The study objective is to compare between skin graft fixation with staples and glue in burn patients. The study is retrospective. It Includes 44 patients that were hospitalized in the burn unit, Rabin Medical Center, Israel with 2nd and 3rd degree burns, total body surface area 1-50% during 1/2002-5/2003.All patients were operated for debridement and skin grafting. In 29 patients the skin graft was fixated with staples and in 15 with cyanoacrylate glue (histoacryl). The parameters that will be compared are skin graft take, hospitalization length and local infection. |
||||
Detailed Description | |||||
Study Type ICMJE | Observational | ||||
Study Design ICMJE | Allocation: Random Sample Observational Model: Natural History Time Perspective: Longitudinal Time Perspective: Retrospective |
||||
Biospecimen | |||||
Sampling Method | |||||
Study Population | |||||
Condition ICMJE |
|
||||
Intervention ICMJE | |||||
Study Group/Cohort (s) | |||||
Publications * |
|
||||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
|||||
Recruitment Information | |||||
Recruitment Status ICMJE | Completed | ||||
Enrollment ICMJE | 44 | ||||
Completion Date | May 2003 | ||||
Primary Completion Date | |||||
Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
|
||||
Gender | Both | ||||
Ages | |||||
Accepts Healthy Volunteers | No | ||||
Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
Location Countries ICMJE | Israel | ||||
Administrative Information | |||||
NCT Number ICMJE | NCT00363558 | ||||
Other Study ID Numbers ICMJE | 4133 | ||||
Has Data Monitoring Committee | |||||
Responsible Party | |||||
Study Sponsor ICMJE | Rabin Medical Center | ||||
Collaborators ICMJE | |||||
Investigators ICMJE |
|
||||
Information Provided By | Rabin Medical Center | ||||
Verification Date | May 2003 | ||||
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |