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Wrinkle clinical trials

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NCT ID: NCT05514782 Completed - Wrinkle Clinical Trials

A Clinical Study to Evaluate the Long-Term Efficacy and Tolerability of a Daily Anti-Aging Daily Serum

Start date: September 15, 2021
Phase: N/A
Study type: Interventional

This double-blind, randomized, placebo-controlled, single-center clinical trial was conducted to assess the efficacy and tolerance of an anti-aging daily serum to improve moderate overall photodamage and skin fatigue after 12-weeks of twice-daily used when compared to a placebo-serum (vehicle control). A total of 62 subjects, 34-60 years of age completed study participation.

NCT ID: NCT05476211 Completed - Wrinkle Clinical Trials

Safety and Efficacy of the BTL-785F Device for Non-invasive Reduction of Wrinkles

Start date: March 31, 2022
Phase: N/A
Study type: Interventional

This study will evaluate the clinical safety and the performance of the BTL-785F system for non-invasive treatment of facial wrinkles. The study is a multicenter single-arm, open-label, interventional study. The subjects will be enrolled and assigned into one experimental study arm. The subjects will be required to complete four (4) treatment visits and two follow-up visits.

NCT ID: NCT05450380 Completed - Wrinkle Clinical Trials

Clinical Investigation to Assess Safety and Performance of Dermal Filler of Hyaluronic Acid

Start date: August 2, 2022
Phase: N/A
Study type: Interventional

The objective of this clinical investigation is to assess the safety and performance of dermal filler of hyaluronic acid to provide firmness and counteract sagging for the correction of deep wrinkles and imperfections in the lower two thirds of the face at 2 months post-treatment.

NCT ID: NCT05423873 Completed - Wrinkle Clinical Trials

A Multi-Center, Open-label Study Evaluate the Efficacy and Tolerability of a Dual Skincare Regimen Treatment for Facial Hyperpigmentation and Photodamaged Skin in Patients Exposed to Extrinsic Factors of Aging

Start date: March 17, 2021
Phase: N/A
Study type: Interventional

This open-label, multi-center clinical trial was conducted to evaluate the dual skincare regimen of vitamin C serum and moisturizing sunscreen SPF 45 to improve facial hyperpigmentation and photodamage after 12 weeks of twice daily use in healthy female subjects between 35 - 60 years old. A total of 33 subjects completed study participation.

NCT ID: NCT05388604 Completed - Wrinkle Clinical Trials

Clinical Study To Evaluate Paired Treatment With An Alexandrite Laser And Radiofrequency Microneedling For Facial Aging

Start date: June 15, 2022
Phase: N/A
Study type: Interventional

The intended use of the radiofrequency and microneedling devices used in this study is to assess the efficacy and safety of paired treatment for the treatment of facial aging.

NCT ID: NCT05271136 Completed - Wrinkle Clinical Trials

A Clinical Study to Evaluate the Efficacy of an Anti-Aging Serum

Start date: September 30, 2020
Phase: N/A
Study type: Interventional

This double-blind, randomized, controlled, single-center clinical trial was conducted to assess the efficacy and tolerance of an anti-aging serum to improve moderate overall photodamage and skin fatigue of aging skin after 7 days of twice-daily use when compared to the efficacy of a combination of anti-aging serum and an anti-aging facial moisturizer. A total of 26 female subjects, aged 34-60, completed study participation.

NCT ID: NCT05231681 Completed - Wrinkle Clinical Trials

Study to Identify if Saie Beauty's Under Eye Concealer Works to Improve Under-Eye Skin Appearance and Reduce Imperfections

Start date: February 15, 2022
Phase: N/A
Study type: Interventional

Saie Beauty has developed 'Hydrabeam Sheer Brightening Under Eye Concealer' that is specifically designed for improving under-eye skin health. The concealer is aimed at improving under-eye skin features including hydration, firmness/elasticity, smoothness, and brightness. At the same time, it is aimed at reducing imperfections such as dark circles, skin redness, fine lines, wrinkles, and crow's feet. The aim is to understand and assess the efficacy of treatment from the participants' perspective and to see if the participants reported changes in skin features, dark circles, brightness, fine lines, wrinkles, crow's feet, and other skin imperfections.

NCT ID: NCT05162300 Completed - Wrinkle Clinical Trials

Same-Day Combination of VI Peel and Botox for Correction of Sun Damage, Fine Lines and Wrinkles

Start date: December 8, 2021
Phase: Phase 4
Study type: Interventional

This study is being conducted to improve standards of care in the cosmetic treatment of sun damage, fine lines, and wrinkles. VI Peels® and Botox® have been used cosmetically to improve patient concerns as monotherapies. This study seeks to confirm that the same-day combination creates no additional side-effects and furthermore that patient satisfaction is heightened as a result.

NCT ID: NCT05102617 Completed - Wrinkle Clinical Trials

Post Market Usability Evaluation Of The PicoSure Pro Device

Start date: October 21, 2021
Phase: N/A
Study type: Interventional

The intended use of the PicoSure and PicoSure Pro devices used in this study is to treat additional patients with the new PicoSure Pro device and collect additional data on the devices.

NCT ID: NCT05098912 Completed - Wrinkle Clinical Trials

Comparing Polydioxanone Thread Embedding Acupuncture and Manual Acupuncture for Nasolabial Fold Reduction

Start date: September 8, 2021
Phase: N/A
Study type: Interventional

This study was aimed to compare the effectiveness of polydioxanone thread embedding acupuncture and manual acupuncture on the reduction of the nasolabial fold. One cycle of therapy in the manual acupuncture group (MA) was carried out with 6 sessions of manual acupuncture therapy while one cycle of therapy in the thread embedding acupuncture group (TEA) received 1 single session of thread embedding acupuncture. The outcome of the study was assessed based on the length of the nasolabial fold as measured by a digital vernier caliper, changes in wrinkle severity rating scale, and patient's subjective opinion of her nasolabial fold using visual analog scale. Outcome measurements were carried out after completing 1 cycle, and follow up at 2 weeks, 1 month, 2 months and 3 months after completing 1 cycle.