Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
100 participants
OBSERVATIONAL
2019-04-18
2019-07-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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20-29 Years Old
No interventions assigned to this group
30-39 Years Old
No interventions assigned to this group
40-49 Years Old
No interventions assigned to this group
50-59 Years Old
No interventions assigned to this group
60-69 Years Old
No interventions assigned to this group
70-79 Years Old
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Subject agreeing to complete all study required procedures.
* Subject having given freely and expressly her informed consent.
Exclusion Criteria
* Subject who had been deprived of their freedom by administrative or legal decision or who is under guardianship.
* Subject in a social or sanitary establishment.
* Subject participating to another research on human beings or being in an exclusion period for a previous study.
* Subject who underwent tissue augmentation with dermal fillers including HA, calcium hydroxylapatite, autologous fat, mesotherapy, or other cosmetic procedures (eg, face-lift, laser, photomodulation, intense pulsed light, radiofrequency, dermabrasion, chemical peel, liposuction of the thigh, or other ablative procedures) in the face or thigh within 12 months before study entry or was planning to undergo any such treatment during the study.
* Subject who underwent treatment with botulinum toxins in the face or neck within 6 months of study entry or was planning to undergo such treatment during the study.
* Subject who ever received semi-permanent fillers or permanent facial implants (eg, poly-L-lactic acid, polymethylmethacrylate, silicone, expanded polytetrafluoroethylene) anywhere in the face or thigh, or was planning to be implanted with any of these products at any time during the study.
* Subject with current cutaneous inflammatory or infectious processes (eg, acne, herpes), abscess, an unhealed wound, or a cancerous or precancerous lesion on the face or thigh that could interfere with measurements.
* Subject having changed, started or stopped any hormonal treatment or any treatment likely to have an impact on skin condition (over-the-counter or prescription, oral or topical, or anti-wrinkle products on the face), within 30 days prior to enrollment or is planning to begin using such products during the study.
18 Years
80 Years
FEMALE
Yes
Sponsors
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Allergan
INDUSTRY
Responsible Party
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Principal Investigators
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Siham Rharbaoui, MD
Role: PRINCIPAL_INVESTIGATOR
DERMSCAN - Pharmascan
Locations
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Dermscan-Pharmascan
Villeurbanne, , France
Countries
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Other Identifiers
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2019-602-000
Identifier Type: -
Identifier Source: org_study_id
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