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Clinical Trials: Plastic Surgery


Source: Allergan
Ten year safety study examining rates of rare adverse events, child bearing issues, effects of mammography, MRI compliance and results, and long-term benefit of silicone-filled breast implants. Read More
Last Updated: 06 Oct 2016
Source: Pfizer
The study will compare how well PF-06473871 works versus placebo in reducing skin scarring after scar revision surgery of existing breast scars. The study will also evaluate the safety of PF-06473871 in healthy adult subjects. Read More
Last Updated: 18 Jan 2016
Source: Plastic Surgery Educational Foundation
The aims of the Skin Product Assessment Research study were to (1) develop an infrastructure and process for industry-sponsored, Plastic Surgery Educational Foundation (PSEF) research in facial aesthetic surgery and (2) test the research process by comparing outcomes of the Obagi Nu-Derm System (ODNS) and conventional therapy as treatment adjuncts in ablative facial resurfacing. Read More
Last Updated: 28 Apr 2010
Source: Allergan
An evaluation of the clinical performance of SERI® Surgical Scaffold for soft tissue support in subjects undergoing revision augmentation surgery for increased nipple to inframammary fold distance. Read More
Last Updated: 21 Jan 2016
Source: Serene Medical Inc
The purpose of this study is to evaluate the ability of the Serene RF System to effectively improve the appearance of dynamic glabellar lines and sustain the effect for a minimum of 3 months. Read More
Last Updated: 14 Apr 2016
Source: St Vincent's University Hospital, Ireland
Hypothesis: Plastic wound retractors reduce passage of bacteria from the abdomen to the surgical incision site in abdominal surgery Currently, plastic wound retractors are used in abdominal surgery to facilitate access to the abdominal cavity. This study aims to establish whether they also prevent bacteria crossing from the abdominal cavity to the surgical incision site. Patients undergoing abdominal surgery in which a plastic wound retractor (Alexis®)is ... Read More
Last Updated: 18 Jul 2011
Source: Université de Sherbrooke
Introduction: Currently, bariatric surgery appears to be the most effective treatment to improve the health of morbidly obese population. However, the massive weight loss induced by this intervention can create excess loose skin in various parts of the body contributing to the feeling of failure in their desire to feel better in some patients. Several studies show that people are once again disappointed and dissatisfied with their body appearance due to the ... Read More
Last Updated: 09 May 2016
Source: Allergan
This study will evaluate the incidence of reoperations associated with the use of smooth and textured NATRELLE® INSPIRA® TruForm® 1 and TruForm® 2 devices in patients who have undergone primary breast augmentation. Read More
Last Updated: 21 Jul 2016
Source: Baxter Healthcare Corporation
The purpose of the study is to compare the safety and efficacy of ARTISS versus standard of care in adhering tissue places and reducing seroma/hematoma formation in subjects undergoing abdominoplasty. Read More
Last Updated: 02 Feb 2012
Source: Pacira Pharmaceuticals, Inc
The purpose of this study is to provide a more effective postoperative method of pain control for patients undergoing cosmetic sub-muscular breast augmentation. Appropriate postoperative pain management contributes to faster patient mobilization, shortened hospital stays, and reduced healthcare costs. Read More
Last Updated: 29 Nov 2013
Source: Neodyne Biosciences, Inc.
Neodyne has developed an investigational dressing for post-operative incision care. Neodyne is conducting this research to study whether the investigational dressing, called the Neodyne Dressing, can minimize scar formation in a simple manner. Read More
Last Updated: 16 Dec 2014
Source: Chung-Ang University Hosptial, Chung-Ang University College of Medicine
The purpose of this randomized pilot study is to evaluate the effect of intravenous lidocaine on propofol requirement during BIS (Bispectral index) guided MAC (monitored anesthesia care) in facial plastic surgery. Read More
Last Updated: 04 Nov 2015
Source: St Andrew's Centre for Plastic Surgery
The purpose of this single centre study is to evaluate whether the use of Harmonic Synergy Dissecting Hook (Harmonic Scalpel) in breast reconstruction surgery is superior to conventional diathermy in terms of improving ease and speed of perforator dissection, reducing postoperative pain, days of hospital stay and time taken to return to daily activities. Read More
Last Updated: 15 May 2016
Source: Galatea, Corp
In this post market study a resorbable mesh (GalaFLEX) will be used to reinforce the lifted and imbricated SMAS along the suture lines and spread the load of the SMAS along a greater surface area. GalaFLEX mesh is comprised of resorbable 4-hydroxybutyrate fibers. Read More
Last Updated: 08 Mar 2015
Source: Mentor Worldwide, LLC
The study will evaluate the safety and effectiveness with the Mentor MemoryGel® Larger Size Ultra High Profile (UHP-L) Breast Implants. Read More
Last Updated: 11 Jan 2017
Source: Swanson Center
This prospective controlled study examines the use of Doppler ultrasound as a means to screen elective plastic surgery patients for the presence of deep venous blood clots both before and after surgery. This is a noninvasive technique that is known to be both sensitive and specific for the detection of deep venous thromboses in the lower extremities. This method may make it unnecessary to select patients for prophylactic anticoagulation, which poses ... Read More
Last Updated: 19 Apr 2016
Source: Commons Aesthetic Plastic Surgery
Patients with excessive underarm odor and sweating and/or odor are treated with the VASER system to determine the VASER's effectiveness in reducing underarm sweat and odor Read More
Last Updated: 16 Sep 2008
Source: Medtronic - MITG
The purpose of this study is to evaluate the effect of different suture material on the incidence of suture granuloma. Read More
Last Updated: 23 Oct 2012
Source: National Center for Plastic Surgery, Virginia
The study is a prospective multi-centered cohort study designed to determine the safety and efficacy of AlloMax in immediate expander-based breast reconstruction. Specifically, the study is designed to determine if sterility of human acellular dermal matrix results in a lower incidence of infection and seroma. The study will determine if gamma radiation, as a method of terminally sterilizing human acellular dermal matrix, has a negative impact on graft ... Read More
Last Updated: 10 Jun 2012
Source: Integra LifeSciences Services
The aim of this study is to provide data and the guidelines for the use of IDRT SL in small wounds, acute and chronic (less than 6 months), showing the benefits and the easy to use of this product as a one stage procedure. Read More
Last Updated: 23 Feb 2016
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