Combination Facial Aesthetic Treatment in Millennials

Completed · Phase 2

Conditions studied: Dermatological Non-Disease

In brief

With 63% of consumers willing to consider investing in facial aesthetics and 73% of consumers worldwide expecting to invest in aesthetic treatments in the upcoming year, it is imperative to explore patient satisfaction and psychosocial impact of a multimodal aesthetic treatment in a millennial cohort. The investigators hypothesize that a combination approach to facial aesthetic treatment in a millennial cohort will result in increased patient-reported satisfaction in multiple areas, including perception of aging concerns and quality of life.

Key facts

Study ID

NCT04755595

Run by

State University of New York - Downstate Medical Center

People needed

20

Starts

2021-03-09

Expected to finish

2021-05-19

Last updated by the study team

2025-01-14

Who can join

Age: 24 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Date of birth between January 1, 1981 and December 31, 1996
• Naiveté to facial injections of botulinum toxin and dermal filler
• Desire to receive all three facial cosmetic injectables in the study
• Suitable candidate to receive facial injectables, as determined by clinician judgment
• Provision of written informed consent for all study procedures
• Stated willingness to comply with all study procedures and availability for the duration of the study

You may not qualify if…

• Desire to receive only one or two of the facial injectables
• Dermatologic or medical conditions at the injection sites that may be exacerbated by the study procedures (e.g., severe acne, active infection, open sores or lesions, history of cold sores)
• Pre-existing cardiovascular disease (e.g., heart failure, coronary artery disease)
• Pre-existing swallowing or respiratory disorders (e.g., dysphagia, asthma, COPD)
• Peripheral motor neuropathy disease, amyotrophic lateral sclerosis, or neuromuscular junctional disorders (e.g., myasthenia gravis, Lambert-Eaton syndrome)
• Known hypersensitivity or allergies to any of the components of the administered drugs/devices in the study (e.g., Gram-positive bacterial proteins, lidocaine)
• History of anaphylaxis or multiple severe allergies
• History of a bleeding or coagulation disorder
• Pregnant or breast-feeding
• Current and/or scheduled use of the following medications: immunosuppressants, anticoagulants (e.g., warfarin, heparin, rivaroxaban), antiplatelets (e.g., clopidogrel, ticagrelor, NSAIDs), antibiotics (e.g., aminoglycosides), anticholinergics, muscle relaxants
• Procedures or treatments to the face in the past 14 days (e.g., chemical peel, laser surgery, microdermabrasion)
• Plan to undergo elective cosmetic procedure on the face (e.g., laser surgery, plastic surgery, physician-strength chemical peel) during the study
• Any medical condition(s) that could be compromised by participating in the study

Where it is running

• SUNY Downstate Health Sciences University — Brooklyn, New York, United States

Full record on ClinicalTrials.gov

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