Clinical trials: Cosmetic
Pain, Muscle Rigidity
Investigation on a Topical Cosmetic Pain Lotion (Egyfil) for Stiffness and Pain Relief
The application of a novel topical formulation for the treatment of muscular pain and stiffness (Egyfil), containing hyaluronic acid, SH-Polypeptide-6 and SH-Oligopeptide-1, is investigated to evaluate efficacy and safety in 26…
- Trial name
- NCT05711953
- Testing
- Egyfil Pain Lotion
- Where
- Italy
- Volunteers
- 26 people
- Sponsor
- Contrad Swiss SA
Breast Cancer Female
Cosmetic Outcome, Patient-reported Outcomes, and Reconstruction-related Complications in Breast Cancer Women Treated With or Without Post-mastectomy Radiation Therapy
This study aim to investigate the breast reconstruction outcome after mastectomy with or without radiation therapy from the patient's point of view.
- Trial name
- NCT03523078
- Testing
- Breast reconstructive surgery
- Where
- South Korea
- Volunteers
- 500 people
- Sponsor
- Yonsei University
Breast Cancer
Quilting Sutures After Mastectomy
The use of wound drains after mastectomy is common practice in Belgium. However, placement of suction drainage has several disadvantages.
- Trial name
- BE-Quilt (NCT06415032)
- Testing
- Mastectomy with Quilting sutures without drain placement, Mastectomy with Conventional sutures with drain placement
- Where
- Belgium
- Volunteers
- 296 people
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
Cosmetic Outcome, Infection
Sutures Versus Glue in Laparoscopic Port Site Closure.
Cosmesis postoperatively is an important consideration for both patients and surgeons and consequently surgeons have become increasingly interested in replacing conventional sutures by means of adhesive bonds for the closure of…
- Conditions
- Cosmetic Outcome, Infection, Cost
- Trial name
- STILS (NCT03843866)
- Testing
- 4-0 Monocryl, Adhesive Glue
- Where
- Ireland
- Volunteers
- 200 people
- Sponsor
- St. James's Hospital, Ireland
Aesthetic Procedures, Cosmetic Techniques
Expert Consensus on the Clinical Use of Skin Boosters: A Delphi-Based Recommendation Framework
This consensus research project aims to develop standardized, evidence-based recommendations for the clinical use of skin boosters in aesthetic dermatology.
- Conditions
- Aesthetic Procedures, Cosmetic Techniques, Skin Ageing
- Trial name
- NCT07296601
- Where
- Egypt
- Volunteers
- 15 people
- Sponsor
- Venus Research Center
Skin Hyperpigmentation, Dry Skin; Eczema
Efficacy and Safety Assessment of Niacinamide Cosmetic Preparation: a Randomized Controlled Trial
Niacinamide in lower concentrations has been recognized as a cosmetic ingredient with hydrating properties. Therefore, aim was to test the efficacy and safety of niacinamide cosmetic preparation in A Randomized, Controlled Trial.
- Trial name
- NCT06189105
- Testing
- miss alice face it you love me serum, No treatment (usual skincare rutine)
- Where
- Croatia
- Volunteers
- 25 people, healthy volunteers welcome
- Sponsor
- University of Split, School of Medicine
Atopic Dermatitis
Exploratory Study on Lactibiane Topic AD on Skin Flora and Barrier Reinforcement in Mild to Moderate Atopic Dermatitis
This exploratory study aims to evaluate the impact of a cosmetic product (Lactibiane Topic AD) vs placebo on skin flora and skin reinforcement barrier in mild to moderate atopic dermatitis using biometrological, biological and…
- Trial name
- NCT04728269
- Testing
- Lactibiane Topic AD
- Where
- France
- Volunteers
- 10 people
- Sponsor
- PiLeJe
Hyperpigmentation, Dark Spots
A 16-week Clinical Study Investigating a Dark Spot Corrector Serum in Women With Moderate Discrete Hyperpigmentation
This was a single-center, double-blinded, randomized, controlled cosmetic clinical trial to investigate the efficacy and tolerance of dark spot corrector serum and regimen skincare products when used over the course of 16 weeks…
- Trial name
- NCT07468175
- Testing
- Cosmetic dark spot corrector serum
- Where
- United States
- Volunteers
- 48 people, healthy volunteers welcome
- Sponsor
- Revision Skincare
Breast Carcinoma
Cosmetic Evaluation of Lumpectomy Versus Oncolytic Mammoplasty With Bilateral Breast Reduction for Early Stage Breast Cancer
This study will evaluate the cosmetic outcome and examine factors contributing to cosmetic outcome in women treated with lumpectomy or bilateral breast reduction mammoplasty/mastopexy (BRM) followed by hypofractionated whole…
- Trial name
- NCT01400399
- Where
- 3 sites in United States
- Volunteers
- 84 people
- Sponsor
- Coastal Carolina Radiation Oncology
Breast Cancer
Proton Accelerated Partial Breast Irradiation
This prospective, non-randomized phase II study will evaluate the cosmetic outcome of using pencil beam scanning proton therapy for partial breast irradiation in patients diagnosed with early stage breast cancer.
- Trial name
- APBI (NCT03940248)
- Testing
- Proton Accelerated Partial Breast Irradiation
- Where
- United States
- Sponsor
- University of Cincinnati
Rhytides
Effective OnabotulinumtoxinA Dose Response Study for Upper Facial Wrinkles
This research is being done to determine if lower doses of botox than what is currently recommended can give similar results to patients, at lower cost and lower risk to them.
- Trial name
- NCT04994990
- Testing
- OnabotulinumtoxinA Standard Dose, OnabotulinumtoxinA Half Standard Dose
- Volunteers
- healthy volunteers welcome
- Sponsor
- Northwell Health
Immediate Post-Treatment Care, Aging Mid-Face
Post-market Cosmetic Evaluation of Ariessence™ Pure PDGF+ Following Ablative Laser
ariessence is intended to be used as a viscous, leave-on solution designed for topical application to the face. It is intended to be used following non-medical cosmetic procedures, performed by licensed healthcare professionals…
- Conditions
- Immediate Post-Treatment Care, Aging Mid-Face, Aging
- Trial name
- NCT07718347
- Testing
- ariessence pure PDGF+™ is a sterile aqueous formulation containing Hyaluronic Acid and pure platelet-derived growth factor (PDGF).
- Where
- 2 sites in United States
- Volunteers
- 21 people
- Sponsor
- Lynch Regenerative Medicine
Myopia
Comparison of Clinical Performance and Subjective Preference of Three Contact Lenses
The purpose of this study is to evaluate the clinical performance and subject's preference out of three LRE (Limbal Ring Enhancing) lens types: etafilcon A (Johnson\&Johnson), methafilcon A (Interozzo), and methafilcon A…
- Trial name
- NCT03134599
- Testing
- etafilcon A, methafilcon A - Interozzo, methafilcon A - CVI (CooperVision)
- Where
- South Korea
- Volunteers
- 60 people
- Sponsor
- CooperVision, Inc.
Skin, Skin Ageing
Clinical Trial to Assess the Efficacy and Safety of a Cosmetic Product in Individuals Showing Signs of Cutaneous Aging.
This clinical study investigates the effects and safety of a topical cosmetic product containing postbiotics (Bifida ferment extract and Pediococcus ferment extract) in women aged 35-60 with visible signs of skin aging.
- Conditions
- Skin, Skin Ageing, Fine Lines, Face Aging/Photo Aging of Moderate Grade
- Trial name
- SkinMeter (NCT07343544)
- Testing
- Active cream
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- AB Biotics, SA
Acne
A Comparative Study of Cosmetic Product in Subjects With Facial Acne During an Associated-treatment Phase Followed by a Maintenance Phase
In this study, we are interested in the global benefit of the tested product as complementary care to a topical medical treatment during a 3 month-associated treatment phase followed by a 3 month-maintenance phase, compared to a…
- Trial name
- NCT06716398
- Testing
- Test product, Comparator product
- Where
- Brazil
- Volunteers
- 60 people
- Sponsor
- Pierre Fabre Dermo Cosmetique
Cesarean Section, Pain
Double Knots Versus Triple Knots Facia Closure Method; is There a Difference in Pain Sensation or Cosmetic Satisfaction?
The study included women who were scheduled for an elective or had an emergency cesarean section. Age, body mass index (BMI), obstetric history, education status, smoking status and C-section indications of the patients were…
- Conditions
- Cesarean Section, Pain, Cosmetics Sensitivity
- Trial name
- NCT06303817
- Testing
- Double knots facia closure method during cesarean section, Triple knots facia closure method during cesarean section
- Where
- Turkey (Türkiye)
- Volunteers
- 203 people, healthy volunteers welcome
- Sponsor
- Adana City Training and Research Hospital
Injection; Complications, Sepsis, Injection Site Disorder
Transgender, Silicone and Blood Smear
This cross-sectional monocentric study will describe transgender men transitioning into women and who had cosmetic silicone injection.
- Conditions
- Injection; Complications, Sepsis, Injection Site Disorder, Injection Site Extravasation, Intentional Poisoning by Silicone
- Trial name
- TSBS (NCT02580760)
- Where
- France
- Volunteers
- 66 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Wound of Skin, Wound Heal
Efficacy and Safety of 0.25% Timolol Gel in Enhancing Full Thickness Skin Grafts Healing and Cosmetic Outcomes
The use of topical beta-blockers, such as 0.25% timolol, in promoting wound healing is currently emerging in the academic literature.
- Conditions
- Wound of Skin, Wound Heal, Surgical Wound, Full Thickness Skin Graft Healing
- Trial name
- FTSG (NCT03579160)
- Testing
- 0.25% timolol gel with full-thickness skin grafts, Vaseline dressing
- Where
- United States
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Brigham and Women's Hospital
Mild to Moderate Atopic Dermatitis
A Controlled Study to Evaluate the Efficacy and the Tolerability of a Cosmetic Active Ingredient Intended for Subjects With Atopic Dermatitis
Evaluation of safety and clinical efficacy of an active ingredient versus placebo for the treatment of mild to moderate Atopic Dermatitis (AD) adults.
- Trial name
- NCT05057351
- Testing
- Isopentenyltheophylline 0.44% + Glycerin 4.56%, Glycerin 4.56%
- Where
- Italy
- Volunteers
- 44 people
- Sponsor
- Greenpharma S.A.S.
Acne
EVALUATION OF THE EFFICACY OF COSMETIC PRODUCT IN ADULTS SUBJECTS WITH MILD TO MODERATE ACNE
EVALUATION OF THE EFFICACY OF COSMETIC PRODUCT IN ADULTS SUBJECTS WITH MILD TO MODERATE ACNE. USE TEST UNDER DERMATOLOGICAL CONTROL. THE STUDY CONDUCTED IN POLAND AND MAURITIUS
- Trial name
- NCT07107854
- Testing
- cosmetic: EFFACLAR ULTRA CONCENTRATED SERUM
- Where
- Poland
- Volunteers
- 110 people, healthy volunteers welcome
- Sponsor
- Cosmetique Active International