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The study to evaluate the efficacy and safety of Bipolar Radiofrequency-Assisted Lipolysis for cheek and nasolabial fold Contouring

Phase 4
Recruiting
Conditions
Healthy patient
Bipolar Radiofrequency-Assisted Lipolysis, Cheek and nasolabial fold Contouring
Registration Number
TCTR20230515001
Lead Sponsor
ASTRACO MEDICAL NETWORKS LTD.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
39
Inclusion Criteria

1. Aged 25-60 years
2. Both men and women
3. mild to moderate wrinkle 4. BMI 18-29.9

Exclusion Criteria

1. Pregnancy or lactation
2. Subject with underlying disease of coagulopathy, platelet dysfunction, cancer, immunocompromised host, epilepsy or psychiatric disease
3. Subject with cardiac pacemaker or metal equipment in body
4. current smoking or heavy alcoholism
5. Dermatitis or infection at face
6. History of anesthesia drug allergy
7. History of taking coagulopathy drug
8. History of isotretinoin or energy based deviced in 6 month before joining the research
9. History of botulinum toxin injection, filler in 12 month before joining the research
10. History of keloid

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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