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Surgical Scar clinical trials

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NCT ID: NCT04928443 Not yet recruiting - Surgical Scar Clinical Trials

The Management of Surgical Scars Around Knee After Pediatric Orthopedic Surgery: an Observational, Case-control Study

Start date: August 15, 2021
Phase:
Study type: Observational

Scar is an unpleasant symptom that commonly appear after orthopedic surgery, especially the joint procedure. Due to the wide motion range, skin around joint has excessive tension that may increase risk for wide or conspicuous scar formation of surgical wound. Noticeable scar can negatively impact the quality of life and psychosocial development. However, scar management is overlooked in early recovery period easily. Patients commonly start to turn their attention to the surgical scar after the completion of rehabilitation or the resolution of disease or unbearable symptom. It is always beyond the best period of scar treatment, 3 to 6 months after wound healing. This study is aimed to observe and evaluate the scar formation with or without aggressive management in pediatric population within 6 months after wound healing.

NCT ID: NCT03467724 Completed - Breast Augmentation Clinical Trials

Treatment of Surgical Scars Following Breast Augmentation, Abdominoplasty or Face Lift

Start date: January 23, 2018
Phase: N/A
Study type: Interventional

Split-body/face evaluator-blind study of the safety and performance of fractional RF for the treatment of surgical scars following breast augmentation, abdominoplasty or face lift. The study will enroll up to 50 female subjects requesting treatment of surgical scars following breast augmentation or abdominoplasty and up to 25 male and female subjects requesting treatment of surgical scars following face lift surgery. Subjects will receive a total of three treatments of their surgical scars at one-month intervals on one side of the body or face only. Subjects will be followed up at one, two, three and ten months after their last treatment. Outcomes will be compared to the non-treated side.

NCT ID: NCT01883414 Terminated - Surgical Scar Clinical Trials

Feasibility Study: Evaluation of the Ulthera® System for Improvement of Surgical Scars.

Start date: June 2013
Phase: N/A
Study type: Interventional

Up to 25 subjects will be enrolled. Enrolled subjects will received on Ulthera® treatment on one half of their surgical scar. Follow up visits will occur at 30, 90 and 180 days after treatment. Study images will be obtained before treatment, immediately after treatment and at each follow-up visit.

NCT ID: NCT01789346 Completed - Scar Clinical Trials

Pilot Study of a Novel 532nm KTP Laser for the Treatment of Fresh Surgical Scars

Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of the 532nm potassium titanyl phosphate (KTP) laser in comparison with the 595nm pulsed-dye laser (PDL) for the treatment of fresh surgical scars.

NCT ID: NCT01158196 Recruiting - Keloid Clinical Trials

Safety and Efficacy of Infrared Diode Laser on Improvement of Scar and Prevention of Recurrence of Excised Keloid

Start date: June 2010
Phase: Phase 3
Study type: Interventional

A pilot study will be conducted on 2 type of subjects, one with plastic surgery scar with a randomization of laser treated portions, and other with keloid excision scar with a complete laser treatment. The aim is to evaluate the infra-red diode laser influence on keloid recurrence and scar prevention. The keloid recurrence rate will be evaluated at each visit, and the scar prevention in plastic surgery will be evaluated comparing laser treated portion and non-treated portion.