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Oral Surgery clinical trials

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NCT ID: NCT02647606 Completed - Oral Surgery Clinical Trials

Comparison of the Videolaryngoscopes With Manual In-line Stabilization

Start date: January 2016
Phase: N/A
Study type: Interventional

Videolaryngoscope is useful to improve the laryngeal view, especially during difficult intubation. There are several kinds of videolaryngoscopes and it is applicable during nasotracheal intubation. In this study, the investigators will compare the McGrath videolaryngoscope and Pentax-AWS with Macintosh laryngoscope for nasotracheal intubation in patients with manual in-line stabilization.

NCT ID: NCT02426515 Completed - Oral Surgery Clinical Trials

Cryotherapy to Improve Outcomes in Lower Third Molar Surgery

COOL
Start date: August 2015
Phase: N/A
Study type: Interventional

This study is looking to see whether cooling the face using a special cooling device (Hilotherm®) before and during the removal of wisdom teeth will reduce the pain and discomfort patients feel after the procedure. The surgical removal of lower third molars (wisdom teeth) is arguably the most commonly performed surgical procedure worldwide. If this study shows that application of cold before and throughout the procedure is a simple way to reduce post-operative symptoms, it could benefit thousands of patients every year.

NCT ID: NCT02273999 Completed - Pain Clinical Trials

Pulsed Electromagnetic Fields for Postoperative Pain: a Linical Trial in Humans

Start date: September 2012
Phase: N/A
Study type: Interventional

This randomized clinical trial was designed to assess the clinical efficacy of Pulsed electromagnetic field PEMF delivered with a wearable device in terms of postoperative pain and quality of healing after mandibular third molar extraction. The sample included 120 patients undergoing unilateral mandibular third molar extraction. The devices were positioned over the area corresponding to the extraction site and wearers were asked to keep them in place for 7 days. All patients were asked to record pain (on a visual analog scale [VAS]), hours of wearing the device (groups T and P), and any use of analgesics. At 7 days, healing complications (dehiscence, tumefaction, pus, local lymphadenopathy, pain on palpation, postoperative bleeding, alveolitis) were recorded blindly.

NCT ID: NCT02221557 Completed - Oral Surgery Clinical Trials

Case Series of New Alloplastic Bone Graft Material

Start date: March 2015
Phase: N/A
Study type: Interventional

A case series to compare the handling and effectiveness of two different treatment approaches using a new alloplastic bone graft material in ridge preservation compared to allograft existing historical data.