Skin Quality

4

Review clinical trials related to Skin Quality. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Prospective Clinical Investigation to Evaluate the Safety and Effectiveness of Juläine™ in Improving Gluteal Skin Laxity in Adults.

This study aims to evaluate the safety and effectiveness of Juläine™ (poly-L-lactic acid) injections for the treatment of buttock skin laxity. Participants will be randomized to an immediate-treatment group or a delayed-treatment group. The immediate-treatment group will receive 2 to 3 treatment sessions over up to 2 months and will be compared with the delayed-treatment group during the control period; the delayed-treatment group will receive the same treatment after the delay. The primary objective is to assess clinical improvement in buttock skin elasticity 6 months after the last treatment, defined as an increase in skin elasticity measured by a cutometer. Total study participation is up to 16 months, including follow-up. This multicenter trial will be conducted in Brazil.

Participants needed: 100
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Nordberg Medical ABUpdated: Mar 19, 2026
Eligibility criteria

Adults aged 18 to 55 years; [+4]

Pregnancy or breastfeeding, or planned pregnancy/lack of adequate contraception... [+20]

Status: Not yet recruiting

Objective Evaluation of Intradermal MSC-Derived Exosome Therapy on Facial Skin Quality

This study aims to evaluate the potential effects of mesenchymal stem cell-derived suspended exosome therapy on facial skin quality using objective imaging analysis. Thirty adult participants will receive intradermal exosome applications in three treatment sessions performed at one-month intervals. Facial skin analysis will be conducted using the VISIA imaging system before each treatment session and six months after the final treatment. The study will examine changes in multiple facial skin characteristics including wrinkles, pigmentation, skin texture, pores, UV spots, red areas, brown spots, and porphyrins to determine whether exosome therapy may improve overall facial skin quality.

Participants needed: 30
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Mert ErsanUpdated: Mar 12, 2026
Eligibility criteria

• Adults aged 18 to 65 years [+4]

Pregnancy or breastfeeding [+7]

Status: Not yet recruiting

A Study to Evaluate the Efficacy of Collagen 16 Serum Alone, Against and as an Adjunct to Radiesse® Biostimulation Procedure in Female Trial Participants With Aged Skin

This study aims at assessing the efficacy of improving skin aging signs of a serum containing collagen 16 combined with a biostimulation device in healthy female subjects aged between 30 and 70 years over a period of 13 weeks.

Participants needed: 180
Trial details
Age: 30-70Biological sex: FemaleType: InterventionalSponsor: Vichy LaboratoiresUpdated: Mar 3, 2026
Eligibility criteria

Female trial participants aged from 30 to 70 years. [+6]

Trial participants who are pregnant, breastfeeding, or planning to become pregna... [+10]

Status: Not yet recruiting

A Study to Evaluate the Safety and Effectiveness of Kytogen Defend in Facial Skin Quality Improvement in Adult Participants

This study was designed to evaluate the efficacy and safety of KIO021, an injectable solution for carboxymethyl chitosan, for temporary improvement of facial skin condition. Designed for forward-looking effectiveness. To achieve this, it is planned that 500 subjects with dry skin and dull complexion on the face will be included in the injection.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Sinclair Pharmaceuticals LimitedUpdated: Sep 17, 2025
Eligibility criteria

(1) Subjects ≥18 years (subject to the time of signing the ICF), without any res...

(1) Subjects who have known allergies to Carboxymethyl Chitosan Solutions or any...