Status:
COMPLETED
Evaluation of Safety and Efficacy of Using Venus Freeze™ (MP)2 V2 System for Wrinkles Rhytides and Cellulite Treatment
Lead Sponsor:
Venus Concept
Conditions:
Wrinkled Structure
Circumference Reduction
Eligibility:
All Genders
30+ years
Phase:
NA
Brief Summary
Skin aging is a multifactorial process involving the 3 layers of the skin: Epidermis, dermis and hypodermis. Radio-frequency (RF) devices have been used for many years for a variety of surgical appli...
Eligibility Criteria
Inclusion
- Healthy males and females age 30 and up
- Subjects with Fitzpatrick 4 to 9 degrees of elastosis
- Subject able to comprehend and give informed consent for participation in this study
- Subject must commit to all treatments and follow-up visits
- Subject must sign the Informed Consent Form
Exclusion
- Subjects with implanted pacemakers, arrhythmias or any other severe known heart disorder
- Subjects with any implantable metal device in the treatment area
- Subjects on any medication that would affect the characteristic of the skin (medical or hormonal), such as "Accutane", within the past 6 months or photosensitizing medications
- Subjects that have had any other invasive or non invasive method of skin therapy or hair removal performed in the past 9 months (in the treated area) Subjects who are scheduled or planned for any other invasive or non invasive method of skin therapy or hair removal in the treated area at the period of the study
- Subjects who have any form of malignant skin cancer on the treatment area
- Subjects with history of keloid formations or hypertrophic scarring
- Pregnant or lactating Subjects
- Subjects with Epilepsy or severe migraines
- Subjects with permanent makeup/ tattoo/ body piercing (in the treated area)
- Subjects with any Infection / abscess / dermatitis/ pains in treatment target area.
- Subjects who suffer from autoimmune disorders or diabetes
- Subjects with clotting disorders
- Subjects are suffering from psychiatric disorders and treated with psychiatric medications.
- Subject is suffering extreme general weakness.
- Subject objects to the study protocol
- Concurrent participation in any other clinical study
- Physician objection
Key Trial Info
Start Date :
December 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2014
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT01234259
Start Date
December 1 2010
End Date
September 1 2014
Last Update
April 16 2020
Active Locations (1)
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1
Sourasky medical Centre
Tel Aviv, Israel, 64239