CompletedPhase 4NCT05932732
Trial Assessing the Impact on Facial Skin Quality, Hydration, and Skin Barrier of Three (3) Hydrafacial Treatments in Adults of All Skin Types.
Studying Cutis laxa
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
- Austin Institute for Clinical Research
- Principal Investigator
- Edward Lain, MD, MBA, M.DAustin Institute for Clinical Research
- Intervention
- HydraFacial Syndeo System(device)
- Enrollment
- 27 enrolled
- Eligibility
- 30-55 years · All sexes
- Timeline
- 2023 – 2024
Study locations (2)
- Austin Institute for Clinical Research, Inc., Houston, Texas, United States
- Austin Institute for Clinical Research, Inc., Pflugerville, Texas, United States
Collaborators
The HydraFacial Company
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.
Open NCT05932732 on ClinicalTrials.gov