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Tooth, Impacted clinical trials

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NCT ID: NCT03785756 Completed - Pain Clinical Trials

Efficacy of 300 mg Ibuprofen Prolonged-Release Tablets for the Treatment of Pain After Surgical Removal of Impacted Third Molars

Start date: April 29, 2019
Phase: Phase 3
Study type: Interventional

This is a single centre, randomised, double-blind, double-dummy, parallel group, multiple-dose, active and placebo-controlled efficacy study to evaluate the efficacy and safety of 2×300mg ibuprofen Prolonged Release (PR) tablets in subjects with postoperative dental pain.

NCT ID: NCT03784638 Completed - Clinical trials for Impacted Third Molar Tooth

Comparison of Two Different Flap Designs for Bilateral Impacted Mandibular Third Molar Surgery

Start date: November 30, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to compare the effects of lingually-based triangle flap design and buccally based triangular flap design on postoperative swelling, trismus pain after mandibular third molar surgery.

NCT ID: NCT03752255 Completed - Clinical trials for Impacted Third Molar Tooth

Verbal and Visual Information Techniques on Anxiety in Third Molar Surgery

Start date: November 21, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate preoperative anxiety levels using dental anxiety scale (DAS) and the Spielberger State-Trait Anxiety Inventory (STAI).

NCT ID: NCT03747237 Completed - Clinical trials for Impacted Third Molar Tooth

Assessment of the Relationship Between Edema Measurement Methods After Impacted Mandibular Third Molar Surgery.

Start date: November 15, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the correlation between two point distance measurements performed by surgeon on patients face with foldable ruler, which is the most commonly used method, and the subjective scoring will be done by the patient with the help of the edema scale, for measuring edema.

NCT ID: NCT03741894 Recruiting - Clinical trials for Impacted Third Molar Tooth

Examination of the Prevention and Treatment Modalities of Alveolitis in Relation With Impacted Teeth Surgery

AITS
Start date: September 1, 2018
Phase: Phase 4
Study type: Interventional

In the everyday clinical practice the incidence of minor complications is approximately 15-20% of the total number of third molar removals. Alveolitis (dry socket syndrome) may arise in 30-40% of the surgical tooth removals. Several preventive approaches are known, such as the use of iodoform gauze, zink-oxide eugenol paste, platelet rich fibrin (PRF), different medicine containing pastes, like antibiotics containing, non-steroid pain killer containing, steroid containing, or the application of chlorhexidine gel and solutions. In the case of a manifest alveolitis these methods can be used as well. The aims of this research are: i) to identify the important pathogens which play role in the development of alveolitis (microbiological methods), ii) to analyze the in vitro effectivity of the different antiseptic materials in case of infections (inhibitory zones) iii) to compare the effectivity of different alveolitis preventive methods in a prospective clinical study, iv) to compare the different treatment options in alveolitis in a prospective clinical study.

NCT ID: NCT03678805 Completed - Impaction of Tooth Clinical Trials

The Effect of Surgical Interventions to Assist Orthodontic Movement of Impacted Maxillary Canines

Start date: July 2, 2018
Phase: N/A
Study type: Interventional

Impacted canine causes many problems for patients, such as absorption and damages to the adjacent teeth roots, as well as aesthetic problems. Correction of this problem requires a lengthy time. Therefore, many methods have been suggested to accelerate the movement of impacted canines with the help of surgical procedures.

NCT ID: NCT03672669 Completed - Pain, Postoperative Clinical Trials

Comparison of the Effect of A-PRF and L-PRF on Outcomes After Removal of Impacted Mandibular Third Molar

Start date: November 5, 2017
Phase: N/A
Study type: Interventional

In this study, it was aimed to investigating and comparing the postoperative effects of leukocyte- and platelet-rich fibrin (L-PRF) and advanced platelet-rich fibrin (A-PRF) in terms of pain, swelling on the cheek, and trismus after mandibular third molar surgery. The study included a total of 27 patients with bilateral impacted mandibular third molar which surgically operated at different times. Patients were evaluated in two randomly separated groups. For the first group; A-PRF and for the second group; L-PRF was applied into the tooth socket. The outcomes variables were; pain, swelling, the number of analgesics taken, and trismus. These variables were also assessed on the basis of; 1st, 2nd, 3rd and 7th days following the operation.

NCT ID: NCT03619460 Recruiting - Clinical trials for Impacted Third Molar Tooth

Clinical Efficacy of a New Piezoelectric Technique for Wisdom Teeth Extraction

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

the aim of this randomized controlled clinical study is to evaluate the efficacy of a new piezoelectric technique for wisdom teeth extraction without using manual tools versus the conventional one.Patients referred to the hospital of Bolzano for wisdom tooth extraction will be randomly divided in two groups. In the test group all the procedure will be performed using piezoelectric instruments, while in the control one conventional manual instruments will be used. Main outcome measures are patient pain and complications, secondary outcome measures are duration of the surgical treatment and soft tissue healing

NCT ID: NCT03512769 Completed - Clinical trials for Impacted Third Molar Tooth

Feasibility Testing of a New Way to Support the Jaw During 3rd Molar Extractions

Start date: June 1, 2018
Phase:
Study type: Observational

Cross sectional observational study to assess the feasibility of using the functional prototype of the restful jaw support device to support the jaw when extracting mandibular 3rd molars using moderate/deep sedation. An additional meeting(s) will occur, after the oral and maxillofacial surgeons (OMS) have completed all treatment procedures utilizing the device and surveys are completed, to provide feedback on how the device performed.

NCT ID: NCT03492814 Completed - Trismus Clinical Trials

Comparing Different Suturing Techniques on the Post-operative Morbidity After Removal of Impacted Mandibular Third Molar

Start date: March 10, 2016
Phase: N/A
Study type: Interventional

This study compares the effect of two types of suturing techniques in the postoperative swelling and mouth opening after surgical removal of impacted mandibular third molar. total wound closure will be performed in one group of participants while partial closure will be performed in the other group.