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Impacted Third Molar Tooth clinical trials

View clinical trials related to Impacted Third Molar Tooth.

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NCT ID: NCT04438434 Not yet recruiting - Clinical trials for Impacted Third Molar Tooth

Evaluation of Hydrogen Peroxide and Hyaluronic Acid (BMG0703) in the Healing of Post-extraction Sites

Start date: June 2020
Phase: Phase 3
Study type: Interventional

A clinical study to evaluate the efficacy and safety of a mouthwash containing Hydrogen Peroxide, Sodium Hyaluronate and Glycine in the healing of post-extraction sites of wisdom teeth by film forming action.

NCT ID: NCT04424875 Completed - Clinical trials for Impacted Third Molar Tooth

The Effect of Melatonin Application Following Removal of Impacted Third Molar

Start date: July 1, 2020
Phase: Phase 3
Study type: Interventional

In the present study, the main hypothesis hypothesizes that the local application of melatonin in the post-extraction socket produces favorable differences in the immediate postoperative period, as anti-inflammatory, analgesic, and early osteogenic regarding the natural healing process of the socket.

NCT ID: NCT04376268 Active, not recruiting - Clinical trials for Impacted Third Molar Tooth

Comparison of the Efficacy of Boric Acid Mouthwashes in Different Concentrations

Start date: January 15, 2019
Phase: Phase 4
Study type: Interventional

Surgical removal of impacted third molars is one of the most frequent procedures carried out in the oral and maxillofacial surgery clinics. There are a varying range of postoperative complications including pain, edema and swelling. Antibiotics, analgesics and mouthwashes are usually prescribed for the treatment of these complications. Patients undergoing impacted third molar surgery are frequently prescribed chlorhexidine mouthwashes with/without benzydamine hydrochloride. However, there has been a search for alternatives with anti-inflammatory, antibacterial and analgesic properties as part of the oral care routine following surgical removal of impacted third molars. Thus, this multicenter study was aimed to evaluate the effects of chlorhexidine mouthwashes with different boric acid concentrations (%0.1, %0.5, %1, %1.5, %2 and %2.5), and boric acid mouthwash on the postoperative complications and compared with chlorhexidine mouthwash after the removal of impacted wisdom teeth.

NCT ID: NCT04373421 Completed - Clinical trials for Impacted Third Molar Tooth

Effect of St. John's Wort and Olive Oils on the Postoperative Complications

Start date: August 15, 2018
Phase: Phase 4
Study type: Interventional

Surgical removal of impacted third molars is one of the most frequent procedures carried out in the oral and maxillofacial surgery clinics. There are a varying range of postoperative complications including pain, edema and swelling. Antibiotics, analgesics and mouthwashes are usually prescribed for the treatment of these complications. Patients undergoing impacted third molar surgery are frequently prescribed chlorhexidine mouthwashes with/without benzydamine hydrochloride. However, to preclude the adverse effects of these chemical agents, there has been a search for plant-derived alternatives with anti-inflammatory, antibacterial and analgesic properties as part of the oral care routine following surgical removal of impacted third molars. However, there is no study investigating the comparison of different essential oils in the literature. Thus, this multicenter study was aimed to evaluate the effects of St. John's wort oil and virgin olive oil on the postoperative complications and compared with chlorhexidine gluconate plus benzydamine hydrochloride mouthwash after the removal of impacted wisdom teeth.This study was aimed to evaluate the effects of St. John's wort oil, virgin olive oil, and chlorhexidine gluconate plus benzydamine hydrochloride on the postoperative complications after the removal of impacted wisdom teeth.

NCT ID: NCT04366635 Recruiting - Clinical trials for Impacted Third Molar Tooth

Evaluation of Two Different Grafting Techniques After Mandibular Impacted Third Molar Surgery

Start date: April 27, 2020
Phase: N/A
Study type: Interventional

This study evaluates the effectiveness of using Mineralized Plasmatic Matrix and β-tricalcium phosphate that placed to extraction socket as a graft material in terms of periodontal damage occurred in the distal aspect of the second molar after mandibular impacted third molar surgery.

NCT ID: NCT04365088 Active, not recruiting - Clinical trials for Impacted Third Molar Tooth

Evaluation of the Effects of Pre-operative Deflazacort on Post-operative Pain, Edema and Trismus

Start date: December 15, 2018
Phase: Phase 4
Study type: Interventional

Removal of impacted lower third molar teeth is one of the most common oral surgical procedures, and these operations often lead to various complications in patients. Antibiotics, analgesics and/or anti-inflammatory drugs are prescribed for the treatment of complications encountered. Anti-inflammatory is the property of a substance or treatment that reduces inflammation or swelling. Anti-inflammatory drugs make up about half of analgesics, remedying pain by reducing inflammation as opposed to opioids, which affect the central nervous system to block pain signaling to the brain. Based on this information, in this study, it is aimed to evaluate the effects of deflazacort preoperatively on the postoperative pain, swelling and trismus.

NCT ID: NCT04349579 Active, not recruiting - Clinical trials for Impacted Third Molar Tooth

Evaluation of the Effects of Irrigation of the Extraction Socket With Rifamycine

Start date: November 15, 2018
Phase: Phase 4
Study type: Interventional

Removal of impacted lower third molar teeth is one of the most common oral surgical procedures, and these operations often lead to various complications in patients. Antibiotics, analgesics and mouthwashes are prescribed for the treatment of complications encountered. When using postoperative antibiotics in surgery of impacted third molar teeth, lower surgical area infection, pain, swelling and trismus are seen. Based on this information, in this study, it is aimed to evaluate the effects of rifamycine intraoperatively on the postoperative pain, swelling and trismus.

NCT ID: NCT04319978 Not yet recruiting - Clinical trials for Impacted Third Molar Tooth

Dexamethasone Effect on Pain and Edema Following Mandibular 3rd Molar Surgery; Pre-operatively vs Post-operatively

Start date: July 2020
Phase: Phase 4
Study type: Interventional

TThis is a comparative clinical study which will be conducted in OMFS department of DIKIOHS, DUHS Ojha Karachi. In this study the investigators will be comparing the effect of dexamethasone on pain and edema when administered pre-operatively vs post-operatively following surgery of impacted lower 3rd molars. Time duration of this study will be 2 months. A total of 100 patients will be considered in this study which will be equally divided into two groups; group A and group B (50 in each group).Group A will receive dexamethasone 1 hour pre-operatively while group B will receive the same post-operatively. All surgeries will be performed by the same maxillofacial surgeon and duration of surgery will be around 30-45 mins.

NCT ID: NCT04108559 Completed - Clinical trials for Impacted Third Molar Tooth

Comparison of The Surgical Drain Placement With Use of Kinesiologic Tape

Start date: August 26, 2019
Phase: N/A
Study type: Interventional

The investigator's purpose was to compare the effects of the surgical drain and kinesiologic tape applications on postoperative morbidity after mandibular third molar surgery.

NCT ID: NCT03975920 Completed - Clinical trials for Temporomandibular Disorder

Assessing a New Jaw Support Device During Third Molar Extractions

Start date: June 25, 2019
Phase: N/A
Study type: Interventional

During mandibular 3rd molar (wisdom tooth) extractions, when a downward force is placed on the patient's jaw, the patient must tense his/her jaw muscles to oppose it. Patients under moderate/deep sedation or general anesthesia cannot tense their muscles to counter this downward force to prevent injury to the jaw including the temporomandibular joint (TMJ). Bite blocks hold the patient's mouth open but do not counter this downward force on the mandible. Currently, oral and maxillofacial surgeons (OMSs) when surgically removing 3rd molars (wisdom teeth) with moderate/deep sedation or general anesthesia have a dental assistant that stands behind the chair and places their hands on both sides of the jaw to support it and oppose the downward force on the patient's jaw during the extractions. It is hard for the dental assistant to maintain support while anticipating the direction and amount of force placed by the OMS on the patient's jaw during the surgical removal. This may explain the finding that almost a quarter of new onset TMD cases in young adults is associated with 3rd molar removal. This study will look at the use of a jaw support device to provide a stable counterforce to downward forces on the jaw, thus preventing jaw hyperextension and injury to the jaw.