A Post Market Evaluation After Treatment of Nasolabial Folds

This is an open, non-comparative study to evaluate effectiveness and safety of Restylane in correction of nasolabial folds up to 12 months after the initial treatment, and to evaluate the safety of repeat treatment of the nasolabial folds 12 months after the initial treatment.

Study Overview

• Status: Completed
• Conditions: Nasolabial Folds
• Intervention / Treatment: Device: Restylane

• Study Type: Interventional
• Enrollment (Actual): 114
• Phase: Not Applicable

Contacts and Locations

Study Locations

• China
  • Beijing
    • No. 33 Badachu Road, Shijingshan District, Beijing, China
      • Plastic Surgery InstituteNo

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria

• 18 years or older
• Intent to undergo correction of both nasolabial folds
• WRSR 3-4
• Signed informed consent

Exclusion Criteria:

• Markedly indurate defects such as significant mid-face volume loss or prominent commissures.
• Active skin disease, inflammation or related conditions, such as infection, psoriasis and herpes zoster near or in the area to be treated.
• Subjects with known hypersensitivity to any ingredient of the study product or anaesthesia used in the study.
• Concomitant anticoagulant therapy and therapy with inhibitors of platelet aggregation, (e.g. non-steriodal anti-inflammatory drugs, acetylsalicylic acid, Omega 3 and Vitamin E) within 2 weeks prior to treatment, or a history of bleeding disorders.
• Concomitant treatment with chemotherapy, immunosuppressive agents, immunomodulatory therapy (e.g. monoclonal antibodies), systemic or topical (facial) corticosteroids. (Inhaled corticoids are allowed).
• Cancerous or pre-cancerous lesions in the treatment area.
• Subjects who have performed aesthetic facial surgery.
• Tissue augmenting therapy with non-permanent filler or neurotoxin below the lower orbital rim in the last 12 months.
• Facial laser treatment or chemical peeling below the lower orbital rim during the last 6 months.
• Permanent implant or filler, including fat-injections, placed in the area to be treated.
• Women who are pregnant or breast feeding or who are planning to become pregnant during the study period.
• Participation in any other clinical study within 30 days prior to inclusion.
• Any medical condition that in the opinion of the investigator would make the subject unsuitable for inclusion (e.g. a chronic, relapsing or hereditary disease that may affect the general condition or may require frequent medical treatment, psychiatric disorders or subjects not likely to comply to study procedures or to avoid other facial cosmetic treatments below the lower orbital rim).
• Subjects who are study site staff for this study, or close relatives (defined as parents, siblings, children or spouse) of the study site staff, as well as subjects who are employed by the sponsor company, or close relatives of employees at the sponsor company.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Active treatment	Device: Restylane

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Effectiveness of study treatment in correction of nasolabial folds up to 12 months after a single treatment:	Investigator evaluated wrinkle severity using wrinkle severity rating scale (WSRS); Improvement in subject and investigator rated global aesthetic improvement (GAIS) compared to baseline.; Subject satisfaction	up to 12 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants with Adverse Events as a Measure of Safety and Tolerability	Safety of study treatment after single and repeat treatment of nasolabial folds will be assessed by: Local tolerability (reported by subjects in a 14-day diary); Adverse Events	Up to 12 months

Collaborators and Investigators

• Sponsor: Galderma R&D

Study record dates

Study Major Dates

• Study Start: July 1, 2014
• Primary Completion (Actual): January 1, 2016
• Study Completion (Actual): January 1, 2016

Study Registration Dates

• First Submitted: June 19, 2014
• First Submitted That Met QC Criteria: July 1, 2014
• First Posted (Estimate): July 2, 2014

Study Record Updates

• Last Update Posted (Actual): August 25, 2022
• Last Update Submitted That Met QC Criteria: August 24, 2022
• Last Verified: February 1, 2015

More Information

Terms related to this study

• Keywords: Correction of moderate to severe nasolabial folds
• Other Study ID Numbers: 05DF1312