Evaluation of Safety and Efficacy of Using Seraffix LTB - System for Excisional Biopsy Wounds Closure
NCT00525434 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10
Last updated 2011-06-09
Summary
The purpose of this study is to evaluate the safety and effectiveness of using Seraffix LTB system for excisional biopsy wounds closure
Conditions
- Dehiscence, Surgical Wound
Interventions
- DEVICE
-
Seraffix LTB
wounds closure by using laser and albumin
Sponsors & Collaborators
-
Seraffix
lead INDUSTRY
Principal Investigators
-
Yehuda Ullmann, Dr. · RAMBAM Medical Center, Haifa Israel
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-11-30
- Primary Completion
- 2009-07-31
- Completion
- 2009-11-30
Countries
- Israel
Study Locations
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