IRCT20150101020514N24
Recruiting
Phase 2
Evaluating the safety and effectiveness of injectable gel with the Perjunse brand, for correcting nasolabial folds, before and after single clinical trial
Pars Fardad Nano Technology Company0 sites30 target enrollmentTBD
ConditionsSkin aging.
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Skin aging.
- Sponsor
- Pars Fardad Nano Technology Company
- Enrollment
- 30
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •18\-65 year old men and women
- •Moderate to severe nasolabial folds based on Allergan criteria
- •The opportunity to accompany the visit programs and study process.
- •Signing the informed consent form and agree to a 6\-month follow\-up
Exclusion Criteria
- •Previous hyaluronic acid (HA)\-based dermal filler treatment(s) injected within the last 12 months prior to enrollment.
- •Cosmetic facial procedures (chemical peel, laser, radio frequency, dermabrasion, ablative or non\-ablative procedures), Botox) in the lower 2/3 of the face, within 3 months prior to study entry
- •Planning to undergo any of these procedures at any time during the study
- •Any cosmetic facial procedures during last 3 months
- •Allergy to gram positive bacteria protein, gel ingredients
- •Auto immune or immune deficiency diseases
Outcomes
Primary Outcomes
Not specified
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