Manageability and Safety Assessment of Sepraspray in Abdominal Surgery.
NCT00813397 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 210
Last updated 2015-05-22
Summary
This study will examine the performance of SeprasSpray in patients undergoing abdominal surgery (laparoscopic).
Conditions
- Adhesion Prevention
Interventions
- DEVICE
-
Sepraspray
Max. 10g of Sepraspray
Sponsors & Collaborators
-
Genzyme, a Sanofi Company
lead INDUSTRY
Principal Investigators
-
Medical Monitor · Genzyme, a Sanofi Company
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-09-30
- Primary Completion
- 2009-07-31
- Completion
- 2009-07-31
Countries
- France
Study Locations
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