Active, not recruitingNot applicableNCT06202274
Clinical Study to Evaluate the Safety and Efficacy of Candela Technology
Studying Anterior cutaneous nerve entrapment syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Candela Corporation
- Principal Investigator
- Konika P Schallen, MDCandela Institue for Exellence
- Intervention
- Nordlys, Gentle, Picoway, Vbeam, Profound, Profound Matrix, eTwo, Exceed, CO2RE(device)
- Enrollment
- 500 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2029
Study locations (3)
- Center for Morden Aesthetic Medicine, Jacksonville, Florida, United States
- Candela Institue for Excellence, Marlborough, Massachusetts, United States
- Yokneam Candela Clinic, Yokneam Illit, Israel
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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