Evaluating the safety and effectiveness of injectable gel with the Perjunse brand, for correcting nasolabial folds, before and after single clinical trial
Evaluating the safety and effectiveness of injectable gel with the Perjunse brand, for correcting nasolabial folds
Design
Single group, phase 2, before -after clinical study. sample size is 30. The study is not randomized
Settings and conduct
The study will be conducted in Center for research and training in skin diseases and leprosy. Before intervention face photography will be taken from participants using digital camera and Visioface camera for determination the severity of nasolabial folds, according to Allergan scale. Skin ultrasound also will perform on nasolabial folds. One intradermal injection with Perjunse will be performed on each nasolabial fold. The assessment will be repeated right after intervention and 2, 12 and 24 weeks later. Subjects’ satisfaction and adverse effect will be recorded in each follow up visit.
Participants/Inclusion and exclusion criteria
Inclusion criteria: 18 -65 years old men and women, with moderate to severe nasolabial folds, the opportunity to accompany the visit programs and study process.
Exclusion criteria: Previous hyaluronic acid (HA)-based dermal filler treatment(s) injected within the last 12 months;
Cosmetic facial procedures (chemical peel, laser, radio frequency, dermabrasion, ablative or non-ablative procedures), Botox) in the lower 2/3 of the face, within last 3 months.
Intervention groups
Intervention group: One injection with 1-2 cc Perjunse gel in each nasolabial fold. Perjunse is a sterile physiological solution, without fever microbial agent. The active ingredient of this product is 24 mg/ml cross-linked hyaluronic acid with non-animal origin.
Main outcome variables
Severity of nasolabial folds according to Allergan grading
General information
Reason for update
Acronym
IRCT registration information
IRCT registration number:IRCT20150101020514N24
Registration date:2023-10-16, 1402/07/24
Registration timing:prospective
Last update:2023-10-16, 1402/07/24
Update count:0
Registration date
2023-10-16, 1402/07/24
Registrant information
Name
Alireza Firooz
Name of organization / entity
Tehran University of Medical Science
Country
Iran (Islamic Republic of)
Phone
+98 21 8897 8190
Email address
firozali@tums.ac.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2023-10-22, 1402/07/30
Expected recruitment end date
2024-01-20, 1402/10/30
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
Evaluating the safety and effectiveness of injectable gel with the Perjunse brand, for correcting nasolabial folds, before and after single clinical trial
Public title
Safety and effectiveness of injectable gel with the Perjunse brand
Purpose
Treatment
Inclusion/Exclusion 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
Pregnancy
Lactation
Age
From 18 years old to 65 years old
Gender
Both
Phase
2
Groups that have been masked
No information
Sample size
Target sample size:
30
Randomization (investigator's opinion)
N/A
Randomization description
Blinding (investigator's opinion)
Not blinded
Blinding description
Placebo
Not used
Assignment
Single
Other design features
Secondary Ids
empty
Ethics committees
1
Ethics committee
Name of ethics committee
Ethics committee of The Institute of Pharmaceutical Sciences of Tehran University of Medical Science
Street address
Unit 1-219, 2nd floor, The Institute of Pharmaceutical Sciences, Faculty of Pharmacy, 16 Azar Avenue
City
Tehran
Province
Tehran
Postal code
1417613151
Approval date
2023-10-08, 1402/07/16
Ethics committee reference number
IR.TUMS.TIPS.REC.1402.085
Health conditions studied
1
Description of health condition studied
Skin aging
ICD-10 code
ICD-10 code description
Primary outcomes
1
Description
Severity of nasolabial folds
Timepoint
Before intervention and right after intervention and 2, 12 and 24 weeks later
Method of measurement
5 scale Allergan photo numeric grading
Secondary outcomes
1
Description
Depth, area and volume of nasolabial fold
Timepoint
Before intervention and right after intervention and 2, 12 and 24 weeks later
Method of measurement
Visioface camera
2
Description
Thickness and density of dermis
Timepoint
Before intervention and right after intervention and 2, 12 and 24 weeks later
Method of measurement
Skin ultrasound
Intervention groups
1
Description
Intervention group: Intervention group: One injection with 1-2 cc Perjunse gel in each nasolabial fold. Perjunse is a sterile physiological solution, without fever microbial agent. The active ingredient of this product is 24 mg/ml cross-linked hyaluronic acid with non-animal origin.
Category
Treatment - Drugs
Recruitment centers
1
Recruitment center
Name of recruitment center
Center for Research and Training in Skin Diseases and Leprosy