Safety and Performance Evaluation of Tulip Device in Healthy Overweight and Obese Volunteers
NCT01753609 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8
Last updated 2012-12-20
Summary
The study will assess the safety and performance of an intragastric auto-inflating and degradable balloon
Conditions
- Over Weight
- Obesity
Interventions
- DEVICE
-
Tulip capsule
swallowing Tulip capsule for up to 29 days
Sponsors & Collaborators
-
Tulip Medical Ltd.
lead INDUSTRY
Principal Investigators
-
Sigal Fishman, Dr. · Tel Aviv Medical Center
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2013-01-31
- Primary Completion
- 2013-03-31
- Completion
- 2013-07-31
Countries
- Israel
Study Locations
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