Clinical Trials Logo

Impacted Third Molar Tooth clinical trials

View clinical trials related to Impacted Third Molar Tooth.

Filter by:

NCT ID: NCT05548790 Completed - Dental Anxiety Clinical Trials

Should Preoperative Information Before Impacted Third Molar Extraction?

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

The main objective of the present study was to evaluate the effects of different preoperative information techniques (verbal, written, video with background audio, and silent video with subtitles) on patients' anxiety levels before and after third molar extraction. The secondary objective was to determine the superiority of the information methods evaluated over each other. We hypothesized that the information provided by video with or without background audio would decrease preoperative and postoperative anxiety levels more effectively than information provided by verbal and written methods.

NCT ID: NCT05545553 Completed - Clinical trials for Impacted Third Molar Tooth

Piezosurgery and Conventional Rotary Instruments on Third Molar Surgery

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

The aim of this study is to compare piezosurgery and conventional surgery in impacted third molar surgery and to determine its effect on postoperative outcomes and quality of life.

NCT ID: NCT05544539 Completed - Clinical trials for Impacted Third Molar Tooth

the Effect of Ozone Oil on the Postoperative Sequalae After Surgical Removal of Third Molar

Start date: March 21, 2021
Phase: Phase 2
Study type: Interventional

This study aimed to evaluate the effectiveness of intra socket application of Ozone oil on postoperative pain, trismus and facial swelling following the surgical extraction of impacted mandibular third molars.

NCT ID: NCT05540015 Not yet recruiting - Clinical trials for Impacted Third Molar Tooth

Use of Erbium Laser for Extraction of the Third Molars

Start date: December 2022
Phase: N/A
Study type: Interventional

A comparative analysis of the effectiveness of the erbium laser with the wavelength of 2.94 µm and traditional instruments in the extraction of the impacted lower third molars will be performed. Clinical, radiological and biochemical findings will be assessed after extraction of the impacted lower third molars.

NCT ID: NCT05534204 Completed - Clinical trials for Impacted Third Molar Tooth

Evaluation of the Effects of Silk and Polyester Suture on Postoperative Complications

Start date: April 16, 2020
Phase: N/A
Study type: Interventional

Some undesirable complications such as pain, swelling, trismus, paresthesia, hematoma, infection and, albeit rare, fractures may occur after lower impacted wisdom tooth surgery. More effective wound closure methods with fewer complications have positive effects on postoperative recovery. Suturing is the most commonly used wound closure technique after lower impacted wisdom tooth surgery. Suturing, which is the last step of the operation, contributes to wound healing in order to reposition and stabilize the tissue components and to control bleeding. In our study, it was aimed to evaluate the efficacy of silk and polyester sutures used in wound closure techniques, which are frequently used in lower impacted wisdom teeth surgery.

NCT ID: NCT05488028 Completed - Clinical trials for Impacted Third Molar Tooth

3D Evaluation of Facial Swelling Post Impacted Lower Third Molars Surgery: RCT

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

Aim of the study is to evaluate the swelling following the osteotomy when performed with drilling bur versus piezo-electric instrument in the mandibular impacted third molar extraction, using a facial reconstruction software

NCT ID: NCT05414253 Recruiting - Wound Heal Clinical Trials

Evaluation of Chlorhexidine Plus Hyaluronic Acid Mouthwash in Surgical Wound Healing Following Third Molar Surgery (CLOR_4)

CLOR_4
Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Evaluation of the response of gingival tissues to the use of mouthwash with chlorhexidine and chlorhexidine + hyaluronic acid in terms of healing of the surgical wound following third molar surgery.

NCT ID: NCT05385679 Not yet recruiting - Clinical trials for Impacted Third Molar Tooth

Comparison of Two Flaps in Surgical Removal of Impacted Lower Third Molar

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Project summary The surgical removal of mandibular third molar is one of the most common procedures done in oral and maxillofacial surgery. Patients often experience pain, swelling, trismus, dehiscence, alveolar osteitis, infection, nerve injury and periodontal tissue damage after third molar surgery. Flap design is an important step in third molar surgery.The aim of this study is to compare the triangular and envelope flap designs in lower third molar surgery in terms of postoperative sequelae including pain ,trismus,swelling,incidence of dry socket and also operative time taken.The study also aims to find out does the level of impacted mandibular third molar and number of roots has effect on postoperative outcomes in surgical removal of mandibular third molar.The study design used will be a double-blind randomized clinical study. Patients who fit the inclusion criteria will be included as research subjects.Sample will be divided into two groups randomly. In one group the envelope flap will be raised during surgical removal of the lower third molar while in the other triangular flap will be used. Investigators will also divide the third molars into level 1,level 2,level 3 based on the relationship between the tip of mesial cusp of impacted third molar and the distal surface of crown of adjacent second molar based on orthopantomograph findings.Level 1 will be when the tip of mesial cusp of third molar is within the occlusal third of crown of second molar,level 2 will be when the tip of mesial cusp of third molar is within the middle third of crown of second molar, level 3 will be when the tip of mesial cusp of third molar is within and below the cervical third of crown of second molar. Another subgroup will be based on the number of roots of the impacted third molar where investigators will divide the third molar into single rooted and multirooted based on orthopantomograph findings. Investigators will also divide the sample based on gender and age group as below 30 years and above 30 years. The primary outcomes to be measured are pain and operative time while secondary outcomes are swelling ,trismus and incidence of dry socket.Outcome assessment will be done by another clinician than surgeon using scientific tools and techniques as mentioned. Surgical procedures and outcomes measurement will be done by separate clinicians to ensure masking.

NCT ID: NCT05344222 Completed - Clinical trials for Impacted Third Molar Tooth

Effects of Photobiomodulation Conditioning in Impacted Third Molars

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

The removal of third molars should be considered to avoid problems such as cysts and other complications. Surgical intervention with the manipulation of oral tissues has the undesirable postoperative effects of pain, trismus (limited mouth opening) and edema. Photobiomodulation has also proved effective regarding reductions in pain, edema and trismus. The aim of the present study was to evaluate the effectiveness of photobiomodulation for the conditioning of tissues involved in the surgical removal of impacted mandibular third molars in terms of reducing or eliminating postoperative pain, trismus and edema.

NCT ID: NCT05320744 Recruiting - Clinical trials for Impacted Third Molar Tooth

the Relationship Between Various Clinical Variables and Surgical Difficulty of Patients Have Impacted Lower Third Molar

Start date: January 3, 2022
Phase:
Study type: Observational

This study is to evaluate the effect of angle of impaction, impaction depth, and bone density on surgical difficulty of impacted lower third molar, by measuring the angle of impaction, the depth of impaction (Winter's Red line), and bone density (gonial, and antegonial indices) preoperatively by using panoramic radiograph and to correlate the angle, the depth of impaction, and bone density with the surgical difficulty by operation time and surgical technique.