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Face Lift clinical trials

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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: NCT02235363 Completed - Clinical trials for Minimal Invasive Surgery

Thread Lift by Use of Retaining Ligaments

TL
Start date: January 1, 2012
Phase: N/A
Study type: Interventional

In facial rejuvenating surgery, the current trend calls for fewer and less noticeable scars with desired results. Especially to improve the jowls and nasolabial folds, the thread lift is a simple and inexpensive technique for patients who do not wish to undergo the typical facelift surgery, but the weak points of it are less effective and shorter duration than the conventional facelift.The investigators propose the new method of the thread lifting the subdermal and subcutaneous layer with a fiberoptic needle by use of the retaining ligaments with two fixation points on both temporal fascia and retaining ligaments. For the intraoperative evaluation the tensiometer was applied and for the postoperative evaluation the FACE-Q applied.

NCT ID: NCT00999141 Completed - Facial Rhytidectomy Clinical Trials

Efficacy and Safety of FS VH S/D 4 S-apr for Flap Adherence in Rhytidectomy

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare the safety and efficacy of FS VH S/D 4 s-apr versus standard of care in adhering tissue and improving wound healing in subjects undergoing facelift.