NCT03270293

Efficacy and Tolerance Evaluation of a Bio-revitalizing Product Containing Hyaluronic Acid With High and Low Molecular Weight

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 64 (actual)
• Sponsor: Derming SRL · Academic / Other
• Sex: Female
• Age: 30 Years – 60 Years
• Healthy volunteers: Accepted

Summary

Primary end point of the study was to evaluate clinically and by non-invasive instrumental evaluations tolerance and efficacy of a bio-revitalizing product containing hyaluronic acid with high (H-HA) and low (L-HA) molecular weight; the micro-injection of the study product was performed by a specialized dermatologist, bilaterally on the face (zygomatic protuberance, nostril's angle, inferior margin of tragus, lip marionette lines, mandibular angle) of healthy female volunteers aged 30-60 years. It was also aim of this study to evaluate efficacy by the volunteers and tolerance both by investigator and volunteers.

Conditions

• Malar and Sub-malar Volume Deficiency

Interventions

Type	Name	Description
DEVICE	Profhilo

Timeline

• Start date: 2015-03-01
• Primary completion: 2015-07-01
• Completion: 2015-08-01
• First posted: 2017-09-01
• Last updated: 2017-09-05

Locations

1 site across 1 country: Italy