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Nose Deformity clinical trials

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NCT ID: NCT03748459 Completed - Surgical Incision Clinical Trials

Rhinoplasty Scar Comparison

Start date: December 7, 2017
Phase:
Study type: Observational

Traditional suture closure of the columellar scar in rhinoplasty is achieved with permanent skin sutures. These sutures create less inflammation and are thought to lead to improved final scar outcomes. However, permanent sutures require removal which creates pain and inconvenience for the patient. Some surgeons use fast absorbing sutures that do not require removal. The difference in final scar outcome based on suture material used has not been well studied. This study will examine the final scar outcomes of rhinoplasty incisions sutured with traditional permanent suture compared to fast absorbing suture. If scar outcomes are similar between these groups as judged by the patients and blinded observers, rhinoplasty surgeons may be able to preferentially utilize absorbable sutures for incision closure and avoid the pain and inconvenience for the patient during suture removal

NCT ID: NCT03727815 Withdrawn - Nose Deformity Clinical Trials

Effects of Mindfulness Meditation on Rhinoplasty Outcomes

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

A key factor in determining success of facial plastic plastic surgery is overall patient satisfaction. While a number of patient-reported outcomes tools has been developed, there is still limited research in how physicians can improve patient satisfaction and post-operative outcomes. The goal of this study is to investigate the effect of a mindfulness meditation phone application on rhinoplasty outcomes. This study will also explore whether mindfulness meditation is a feasible adjunct to current pharmacological modalities of postoperative pain control as well as its potential impact on patient satisfaction. These questions will be answered using a randomized controlled trial.

NCT ID: NCT03624608 Suspended - Microtia Clinical Trials

Evaluation of the Auryzon Devices in the Optimization of Ear and Nose Reconstruction Procedures

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of the AuryzoN devices in the ear and nose reconstruction surgeries, both in terms of operative time and overall quality of reconstruction. Research participants will undergo reconstruction either using the AuryzoN device or through current methods (traditional manual processing) at the discretion of their surgeon prior to the start of surgery.

NCT ID: NCT02348931 Recruiting - Nose Deformity Clinical Trials

Clinical Effect of a Nasal Former in Nasal Deformities

Start date: December 2013
Phase: Phase 3
Study type: Interventional

Investigation of the effect of customized nasal braces in the correction of nasal deformities with and without prior corrective surgery. - Trial with medicinal product