Post Market Non-Interventional Study of Safety and Performance of RefillHA Volume

NCT ID: NCT07329608

Last Updated: 2026-01-09

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 78 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-01-25
• Study Completion Date: 2025-05-18

Brief Summary

This study designed to evaluate the safety and performance of RefillHA Volume, a dermal filler for facial soft tissue augmentation and correction of facial wrinkles and folds in routine clinical setting.

Detailed Description

This post market study was designed to collect clinical data regarding the safety and performance of RefillHA Volume upon its launch, from patients treated with the product in a routine clinical setting of treatments.

In this study, patients seeking correction of facial wrinkles and folds and/or soft tissue augmentation who are candidates for treatment with RefillHA Volume according to its approved use will be offered to participate in the study. Eligible patients who are willing to participate in the study, after signing an informed consent, will be treated with RefillHA Volume in the facial regions where correction is requested, subject to the advice of the treating physician and in accordance with the approved use.

After recieving initial treatment, participants will attend 2 to 4 in-clinic follow-up visits, during which they were eligible to receive additional treatment with RefillHA Volume (up to two additional treatments during the follow-up period) if, per treating investigator's opinion, additional treatment is required for better correction or to maintain the results.

Clinical data were collected at all in clinic visits, including standardized facial photographs, pain perception self-assessement was recorded by subjects immediately after treatment. All subjects were asked for details of any Adverse Events (AEs) they had experienced. Subjects were asked to rate aesthetic results and Patient Satisfaction questionnaire at each follow-up visit. Physicians were asked to rate aesthetic results as well and details of the treatment session were recorded.

Conditions

Wrinkles

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Subjects over the age of 18

Subjects who are seeking correction of facial wrinkles and folds and/or soft tissue augmentation

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Adult men and women, over the age of 18, seeking correction of facial wrinkles and folds and/or soft tissue augmentation.
• Subjects who are willing and able to read, understand and sign informed consent.

Exclusion Criteria

• Subjects with known contraindications to the treatment (as per device IFU).
• Subjects considered to be unsuitable to participate, in the investigator's opinion, for any reason.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Glyance

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Glyance Ltd

Lod, , Israel

Countries

Israel

Other Identifiers

PMCF-SP-200-01

Identifier Type: -

Identifier Source: org_study_id