Efficacy Study for SD Device
Primary Purpose
Overweight
Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
SD
Control
SD
Sponsored by

About this trial
This is an interventional treatment trial for Overweight
Eligibility Criteria
Inclusion Criteria:
- BMI 30-41.99
- AGE 18-65 years
Exclusion Criteria:
- Pregnant Women,
- Type I and II diabetes,
- People with disfunctioning of thyroid gland
- Hypertension
Sites / Locations
- Emek Medical CenterRecruiting
- Rabin Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Sham Comparator
Experimental
Arm Label
Study arm
Control Arm
Staudy2 arm
Arm Description
The Arm who uses the real study device Daily use of SD device
Daily use of Sham comperator
Uses the under study device in a different time frames Daily use of SD device in a different time frames than of Study Arm
Outcomes
Primary Outcome Measures
Change from Baseline in Body Weight
Each participant's body weight will be measured at his/her beginning of the trial. This measure will become the participant's body weight base-line. Once in every 2 weeks the body weight will be taken again and will be compared to base-line and to previous body weight measures of the participant taken during the study.
Secondary Outcome Measures
Change from Baseline in Waist Circumference
Each participant's Waist circumference will be measured at his/her beginning of the trial. This measure will become the participant's Waist circumference base-line. Once in every 2 weeks the Waist circumference will be taken again and will be compared to base-line and to previous Waist circumference measures of the participant taken during the study.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01534325
Brief Title
Efficacy Study for SD Device
Official Title
Efficacy Study of SD Device for Overweight and Obesity Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Unknown status
Study Start Date
July 2012 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Beck Medical Ltd.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether the SD unique device is effective in treatment of overweight and obesity.
Detailed Description
Obesity and Overweight had become the number 1 health concern of the modern world. Over 1 Billion people worldwide are overweight or obese. Those who suffer from overweight or obesity are exposed to other severe illnesses such as: diabetes, cardiovascular disease and cancer.
Only few drugs and surgeries are currently available as approved treatments for those who wish to reduce weight.
The purpose of this study is to determine whether the SD unique medical device, is effective in treatment of overweight and obesity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Study arm
Arm Type
Experimental
Arm Description
The Arm who uses the real study device Daily use of SD device
Arm Title
Control Arm
Arm Type
Sham Comparator
Arm Description
Daily use of Sham comperator
Arm Title
Staudy2 arm
Arm Type
Experimental
Arm Description
Uses the under study device in a different time frames Daily use of SD device in a different time frames than of Study Arm
Intervention Type
Device
Intervention Name(s)
SD
Intervention Description
The participants in the study receive basic nutrition guidance by MD and clinical dietician and make daily use of the device under study (called SD). During the 13 weeks study period, the participants get to meet clinical dietician/MD once in every 2 weeks for guidance and supervision and for on -going monitoring of physical parameters such as body weight and waist circumference.
The use of the SD device is done by study participants during the day every day throughout the study period. The device under study can be easily used by the participants themselves in their regular environment and does not require professional assistance.
The device under study is expected to affects the satiety, energy homeostasis and metabolic control centers in the brain and by that to reduce food intake and lead to weight loss.
The device under study is a device- not a medication and not a surgical procedure, and it does not involve any of such elements.
Intervention Type
Device
Intervention Name(s)
Control
Intervention Description
The participants in the Control arm of the study receive basic nutrition guidance by MD and clinical dietician and make daily use of the placebo. During the 13 weeks study period, the participants get to meet clinical dietician/MD once in every 2 weeks for guidance and supervision and for on -going monitoring of physical parameters such as body weight and waist circumference.
The use of the placebo is done by the control study participants during the day every day throughout the study period. The placebo can be easily used by the participants themselves in their regular environment and does not require professional assistance.
Intervention Type
Device
Intervention Name(s)
SD
Intervention Description
The participants in the study receive basic nutrition guidance by MD and clinical dietician and make daily use of the device under study (called SD). During the 13 weeks study period, the participants get to meet clinical dietician/MD once in every 2 weeks for guidance and supervision and for on -going monitoring of physical parameters such as body weight and waist circumference.
The use of the SD device is done by study participants during the day every day throughout the study period. The device under study can be easily used by the participants themselves in their regular environment and does not require professional assistance.
The device under study is expected to affects the satiety, energy homeostasis and metabolic control centers in the brain and by that to reduce food intake and lead to weight loss.
The device under study is a device- not a medication and not a surgical procedure, and it does not involve any of such elements.
Primary Outcome Measure Information:
Title
Change from Baseline in Body Weight
Description
Each participant's body weight will be measured at his/her beginning of the trial. This measure will become the participant's body weight base-line. Once in every 2 weeks the body weight will be taken again and will be compared to base-line and to previous body weight measures of the participant taken during the study.
Time Frame
once in every two weeks up to 13 weeks for each participant
Secondary Outcome Measure Information:
Title
Change from Baseline in Waist Circumference
Description
Each participant's Waist circumference will be measured at his/her beginning of the trial. This measure will become the participant's Waist circumference base-line. Once in every 2 weeks the Waist circumference will be taken again and will be compared to base-line and to previous Waist circumference measures of the participant taken during the study.
Time Frame
once in every two weeks up to 13 weeks for each participant
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
BMI 30-41.99
AGE 18-65 years
Exclusion Criteria:
Pregnant Women,
Type I and II diabetes,
People with disfunctioning of thyroid gland
Hypertension
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Beck Medical
Phone
+972-4-62890779
Email
adva@beckmedical.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dror Dicker, MD
Organizational Affiliation
Rabin Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emek Medical Center
City
Afula
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arie Markel, MD
Phone
+972-4-64943400
Email
markel_ar@clalit.org.il
First Name & Middle Initial & Last Name & Degree
Arie Markel, MD
Facility Name
Rabin Medical Center
City
Petach Tikva
ZIP/Postal Code
49100
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dror Dicker, MD
Phone
+972-3-9372426
Email
drord@clalit.org.il
First Name & Middle Initial & Last Name & Degree
Dror Dicker, MD
12. IPD Sharing Statement
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Efficacy Study for SD Device
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