Clinical trials: Contouring
Normal, Healthy Adults With Moderate, Severe, or Very Severe Volume Loss of Anteromedial Malar Region
Clinical Study to Evaluate the Efficacy and Safety of YVOIRE® Contour Compared With Restylane SubQ™ Injected Into the Anteromedial Malar Region
This study is purposed to evaluate the efficacy and safety of YVOIRE® contour compared with Restylane SubQ™ injected into the anteromedial malar region.
- Trial name
- NCT02119780
- Testing
- YVOIRE® contour, Restylane SubQ™
- Where
- South Korea
- Volunteers
- 83 people, healthy volunteers welcome
- Sponsor
- LG Life Sciences
Cheek Augmentation, Correction of Age-related Midface Contour Deficiencies
RHA®4 for Midface Volume Deficiency
This is a prospective, randomized, controlled, blinded evaluator, multicenter, between subjects clinical study to identify whether RHA4 is non-inferior to a comparator device for treatment of midface volume deficiency 8 weeks…
- Trial name
- NCT05133739
- Testing
- injection of RHA®4 in Midface, injection of Comparator Product in Midface
- Where
- United States
- Volunteers
- 201 people, healthy volunteers welcome
- Sponsor
- Teoxane SA
Endosseous Dental Implant Failure, Accident Caused by Broken Ceramic
Full-Contour Monolithic Zirconia Full-Mouth Implant Supported Rehabilitation Behavior
In patients who received a full-mouth implant-supported rehabilitation restored with CAD/CAM full-contour monolithic zirconia (FCMZ, without buccal ceramic veneer; veneering, if present, limited to the gingival area), what is the…
- Trial name
- FCMZ (NCT07876466)
- Testing
- Dental Implant, Monolithic Zirconia (FCMZ)
- Where
- Portugal
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Implantology Institute
Diabetes
Evaluation of Blood Glucose Meter Systems
The purpose of this study was to evaluate the performance of a Bayer Blood Glucose Monitoring System (BGMS) and four additional Blood Glucose Monitoring Systems (BGMS) from other manufacturers.
- Trial name
- NCT01714232
- Testing
- Contour® PLUS BGMS, OneTouch® SelectSimple™ BGMS, Accu-Chek® Performa BGMS
- Where
- United States
- Volunteers
- 106 people, healthy volunteers welcome
- Sponsor
- Ascensia Diabetes Care
Body Fat Disorder
CoolSculpting and EMS for the Abdomen
Evaluate the use of Electromagnetic Muscle Stimulation as an adjunctive treatment to CoolSculpting.
- Trial name
- ECA (NCT03738891)
- Testing
- Zeltiq CoolSculpting System alone, Electromagnetic Muscle Stimulation alone, EMS followed by CoolSculping
- Where
- 4 sites in United States
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Zeltiq Aesthetics
Cellulite, Body Contouring
Evaluation of the Efficacy of Endermologie in Treatment of Cellulite and Body Contouring
The purpose of this study is to perform a clinical assessment of the efficacy of the device DHERMIA® (Industra Mecânica Fina Ltda)in the treatment of cellulite and body contouring
- Trial name
- NCT00399854
- Testing
- Dhermia® - Industra Mecânica Fina Ltda
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- Hexsel Dermatology Clinic
Scar
Efficacy of Natural Vitamin E Tocotrienol on the Treatment of Surgical Scars
The overall goal of this study is to determine the efficacy of tocotrienol (TCT), a natural form of vitamin E, in preventing or reducing scar formation in human skin wounds as well as the basal levels of TCT in normal human skin…
- Trial name
- NCT00700791
- Testing
- Natural Vitamin E Tocotrienol supplement (TCT), Natural Vitamin E Tocotrienol Cream (TCT)
- Where
- 2 sites in United States
- Volunteers
- 168 people, healthy volunteers welcome
- Sponsor
- Chandan K Sen
Cheek Wrinkles, Midface Contour Deficiencies
Safety and Effectiveness of GP0112 for Cheek Augmentation and Correction
A prospective, randomized, evaluator-blinded, comparator-controlled, parallel group, multicenter study to evaluate the safety and effectiveness of GP0112 for cheek augmentation and correction of midface contour deficiencies
- Trial name
- NCT05098457
- Testing
- GP0112, Restylane Lyft Lidocaine
- Where
- 8 sites in Germany
- Volunteers
- healthy volunteers welcome
- Sponsor
- Galderma R&D
Hypotension
The Effect of Intravenous Prehydration on the Hemodynamic Status of Healthy Parturients Undergoing Spinal Anesthesia for Cesarean Delivery
Regional anesthesia (spinal, epidural) is considered the method of choice for anesthesia obstetric deliveries because of the ability to use fewer drugs, a more direct experience of childbirth and the capability to provide…
- Trial name
- NCT01835873
- Testing
- Lactated Ringer's, HES 130/0.42
- Where
- Greece
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- Paraskevi Matsota
Gum Disease
Influence of Implant Crown Transmucosal Contour Design on Soft and Hard Tissue Clinical Outcomes
This study will evaluate how the crown's shape under the gums will influence the gum tissue around dental implants.
- Trial name
- NCT06185075
- Testing
- Implant crown delivery
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- University of Michigan
Surplus Skin After Massive Weight Loss
Complications in Lower Body Lifts
A prospective study on 50 consecutive patients who are going to have a lower body lift procedure is performed. Measures include comorbidities and complications.
- Trial name
- NCT01551862
- Testing
- body contouring surgery of back, abdomen and thighs
- Where
- Austria
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Medical University of Vienna
Diabetes
System Accuracy Evaluation of 6 CE-marked Blood Glucose Monitoring System Following ISO 15197:2013
The objective of this study is the evaluation of system accuracy following ISO 15197:2013 (E), clause 6.3 in which accuracy requirements and applicable test procedures for blood glucose monitoring systems intended for…
- Trial name
- NCT02531386
- Testing
- 6 blood glucose monitoring systems for self-testing (blood glucose meters)
- Where
- Germany
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Institut für Diabetes-Technologie Forschungs- und Entwicklungsgesellschaft mbH an der Universität Ulm
Body Sculpting
A Multicenter,2-Arm,Randomized,Controlled Study Evaluate the Effectiveness of the UltraShape® Contour I VER 3.1 System for Non-Invasive Reduction in Abdominal Circumference
The primary objective of this study is to evaluate the effectiveness of the Contour I VER 3.1 System on abdominal midsection circumference reduction relative to no treatment.
- Trial name
- NCT01462201
- Testing
- Non Invasive Ultrasound
- Where
- 5 sites in United States, Israel
- Volunteers
- 156 people, healthy volunteers welcome
- Sponsor
- UltraShape
Congenital Ptosis
Levator Resection with3 Point Fixation Versus 2 Point Fixation Tucking for Congenital Ptosis
to evaluate the surgical effect of levator aponeurosis resection Versus two point fixation levator aponeurosis Tucking for Congenital Ptosis
- Trial name
- NCT03240107
- Testing
- levator resection, levator tucking
- Where
- Egypt
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Heba Hamdy Ibrahim Mohammed
Post-surgical Scars, Hypertrophic Scars
Surgical Care And Recovery With Laser Evaluation Trial (SCARLET)
The Surgical Care and Recovery with Laser Evaluation Trial (S.C.A.R.L.E.T.) is a prospective, single-center clinical study conducted at AdventHealth Medical Group Plastic and Reconstructive Surgery at Innovation Tower.
- Conditions
- Post-surgical Scars, Hypertrophic Scars, Scar Appearance Dissatisfaction, Aesthetic Surgical Outcomes
- Trial name
- SCARLET (NCT07359352)
- Testing
- ProFractional Laser Therapy and/or Broadband Light (BBL) Treatment
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- AdventHealth
Dental Implant Placement
Volumetric Changes of Labial Soft Tissue Contour Following Different Approaches With Immediate Implant Placement
Statement of the problem: Tooth extraction is followed by ridge alteration and soft tissue contour collapse. Different strategies were proposed to limit this collapse however, the ability of these techniques to mimic the original…
- Trial name
- NCT04310449
- Testing
- Connective tissue graft and customized healing abutment, Dual zone concept and customized healing abutment
- Where
- 2 sites in Egypt
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Misr International University
Juvenile and Adolescent Idiopathic Scoliosis
3-D Correction of Adolescent Idiopathic Scoliosis (AIS) With Differential Metals
This study is designed to evaluate the coronal, sagittal, and axial correction of deformity secondary to adolescent idiopathic scoliosis utilizing a technique employing a posterior spinal fusion construct utilizing rods of…
- Trial name
- AIS (NCT05631821)
- Testing
- differential rod bending with rod contours (MESA Spinal System)
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Rush University Medical Center
Skin Laxity, Lipodystrophy
CONFORM: Rotational Fractional Resection for Submental Contouring
This study will evaluate the safety and efficacy of rotational fractional resection (RFR) to improve neck contouring. RFR is used to remove loose skin and fat.
- Trial name
- NCT03407313
- Testing
- Rotational fractional resection (1.5mm diameter device)
- Where
- 6 sites in United States
- Volunteers
- 68 people, healthy volunteers welcome
- Sponsor
- Recros Medica, Inc.
Fat Reduction, Muscle Tone Increased
Electrical Muscle Stimulation with 1064 Nm Diode Laser and RF/PEMF for Non-invasive Body Contouring and Fat Reduction.
Multi-center, three-arm, randomized, evaluator-blinded study of electrical muscle stimulation (EMS) and/or 1064 nm diode laser, pulsed electromagnetic field (PEMF) and vacuum assisted radio frequency (RF) using the Venus Bliss…
- Trial name
- NCT05256771
- Testing
- EMS, 1064 nm diode laser, RF/PEMF
- Where
- 3 sites in United States
- Volunteers
- 36 people, healthy volunteers welcome
- Sponsor
- Venus Concept
Dental Implant in Compromised Adjacent Sockets
Management of Multiple Adjacent Extraction Sockets
While early implant placement with guided bone regeneration (GBR) offers advantages, the desire for reduced treatment time and fewer surgical steps continues to drive the exploration of alternative approaches.
- Trial name
- VST (NCT07063836)
- Testing
- VST, contour augmentation and early implant placement
- Where
- Egypt
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- British University In Egypt