TCRM for Correction of Cheek Including Fine Lines
NCT07145905 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 130
Last updated 2025-09-08
Summary
The purpose of this clinical study is to evaluate benefits and risks of injecting TCRM in the cheek including fine lines. The goal is to show that treatment with TCRM will result in correcting the cheek area including the fine lines at 4 weeks after last treatment (initial injection or touch up) on subjects.
Conditions
- Skin Aging
- Cheek Wrinkles
Interventions
- DEVICE
-
TCRM
N=128
Sponsors & Collaborators
-
Teoxane SA
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-11-30
- Primary Completion
- 2025-09-30
- Completion
- 2026-01-31
Countries
- Spain
Study Locations
More Related Trials
-
BTL-785F Device for Non-invasive Reduction of Wrinkles
NCT05519124 ·Status: COMPLETED ·Phase: NA
-
Clinical and Histological Evaluation of BTL-785F Device for Non-invasive Treatment of Face
NCT05524662 ·Status: COMPLETED ·Phase: NA
-
Pivotal Study to Evaluate the Safety and Efficacy of a Micro-coring Device Treating Moderate to Severe Facial Wrinkles
NCT03573271 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Micro-excisional Skin Removal by Micro-coring Device in Treatment of Wrinkles and Laxity of Face and Neck
NCT03583918 ·Status: COMPLETED ·Phase: NA
-
Device for Improving Skin Quality and Texture on the Face and Neck
NCT06645366 ·Status: COMPLETED ·Phase: NA
-
Study to Evaluate the Safety and Efficacy of the Cytrellis Micro-Coring Device for the Treatment of Moderate to Severe Facial Wrinkles
NCT03793348 ·Status: UNKNOWN ·Phase: NA
-
A Prospective Pilot Study to Evaluate Safety and Effectiveness of GP0122 and GP0124 for Correction of Lines and Wrinkles in the Cheek Area
NCT07344584 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Investigation of a Novel Cosmeceutical to Reduce the Visible Signs of Cutaneous Aging
NCT02877758 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Evaluation of Safety and Efficacy of the BTL-785F Device for Non-invasive Facial Remodeling
NCT05525026 ·Status: COMPLETED ·Phase: NA
-
Non-invasive Rejuvenation of the Periorbital Area and Lower Eyelid
NCT07028203 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Clinical Trial of Cross-linked Hyaluronic Acid Dermal Filler
NCT05935501 ·Status: COMPLETED ·Phase: NA
-
Investigating Age Dependence of Fibroblast and Extracellular Matrix Responses to Cross-linked Hyaluronic Acid Filler in Human Skin
NCT06195605 ·Status: RECRUITING ·Phase: NA
-
Evaluation of the Effects of a Biostimulator and Dermal Fillers for Cheek Augmentation and Contour Deficiencies
NCT06351358 ·Status: COMPLETED ·Phase: NA
-
BTL-785F Device for Non-invasive Facial Rejuvenation in Patients Injected With Botulinum Toxin
NCT05524766 ·Status: COMPLETED ·Phase: NA
-
Safety Study of Two Repeat Doses of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults
NCT01124565 ·Status: COMPLETED ·Phase: PHASE2
-
Evaluation of Safety and Efficacy of the BTL-785F Device for Non-invasive Reduction of Wrinkles
NCT04447963 ·Status: COMPLETED ·Phase: NA
-
A 4-Arm Efficacy and Safety Study of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults
NCT01124552 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Intradermal Injections of RCS-01 in Male and Female Subjects
NCT02391935 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy and Safety of NT 201 in the Treatment of Lateral Periorbital Wrinkles
NCT00541723 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy of Botulinum Toxin Type A Topical Gel for Lateral Canthal Lines
NCT02580370 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy of the BTL-785F Device for Non-invasive Reduction of Wrinkles
NCT05476211 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal Lines
NCT00968825 ·Status: COMPLETED ·Phase: PHASE2
-
Restylane Silk Microinjections to Cheeks
NCT03742479 ·Status: UNKNOWN ·Phase: NA
-
Safety and Effectiveness Evaluation of TEOSYAL® TPVM Versus COMPARATOR for the Remodeling of the Lower Face
NCT05986630 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal Lines
NCT00888914 ·Status: COMPLETED ·Phase: PHASE2