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Tooth, Impacted clinical trials

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NCT ID: NCT04848259 Completed - Clinical trials for Impacted Third Molar Tooth

Effect of Honey and Dexamethason on Extraction Healing

Start date: January 5, 2021
Phase: Early Phase 1
Study type: Interventional

Natural honey and dexamethason will be given before impaction removal then postoperative complications will be evaluated

NCT ID: NCT04816253 Completed - Clinical trials for Preventing Postextraction Complication

Controlling Post-extraction Complications of Impacted Mandibular Third Molar

Start date: February 10, 2021
Phase: N/A
Study type: Interventional

Impacted mandibular 3rd molar will be extracted in all patients, then patients will be divided, according to material placed in extraction socket into 3 groups: control, hyaluronic acid and honey. Then post extraction complications will be evaluated

NCT ID: NCT04769557 Completed - Clinical trials for Impacted Third Molar Tooth

Pre Emptive Analgesics for Pain Relief in Impacted Lower Third Molar Surgery

Start date: March 4, 2017
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the efficacy of pre-emptive paracetamol in reducing intra operative pressure and post operative pain after surgical removal of impacted mandibular third molar using visual analogue scale

NCT ID: NCT04740450 Completed - Clinical trials for Impacted Third Molar Tooth

Effect of Modified Kinesio Taping Technique on Morbidity After Impacted Third Molar

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

Removal of impacted lower third molar is considered as the most common surgical procedure carried out in the oral and maxillofacial Clinics. The surgical removal of the impacted mandibular third molar is usually associated with pain, swelling and inability to open the mouth. Those symptoms reach the maximum intensity between the third to fifth hours postoperatively for the pain and 24 to 48 hours postoperatively for the swelling and then, they gradually diminished until the 7th day postoperatively

NCT ID: NCT04718077 Completed - Tooth, Impacted Clinical Trials

Intraosseous vs Submucosal Injection of Dexamethasone

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

Thirty-eight patients were randomly divided into 2 groups; the intraosseous injection group of dexamethasone (4 mg) and the submucosal injection group. All surgeries were performed by one surgeon. Postoperative pain was evaluated by visual analog scale score immediately after surgery and on postoperative days 1, 3, and 7. Swelling (determined using two linear measurements) were assessed just before the surgery and on postoperative days 1, 3, and 7 by using a digital vernier caliper. Early healing of periodontal soft tissue wound was assessed by using Early Wound Healing Score (EHS) which composed of 3 parameters: clinical signs of re-epithelization (CSR), clinical signs of hemostasis (CSH), and clinical signs of inflammation (CSI) and were assessed on postoperative days 1, 7, and 14. Mouth opening (determined by measurement of the maximum inter-incisal distance) were assessed just before the surgery and on postoperative days 1, 3, and 7 by using a digital vernier caliper.

NCT ID: NCT04708119 Completed - Pathology Clinical Trials

Histopathologic Changes in Dental Follicle Associated With Radiographically Normal Impacted Lower Third Molars

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

This study aimed to evaluate the incidence of histopathologic changes in dental follicles associated with radiographically normal impacted lower third molar and to determine the relationship between cystic changes in follicle tissues and age, gender, and the angular position of the impacted tooth.

NCT ID: NCT04645888 Completed - Clinical trials for Impacted Third Molar Tooth

Articaine and Bupivacaine in Impacted Tooth Surgery

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

Articaine is a common local anesthetic used in oral surgery and belongs to the amide group of it has fast onset with little side effects. Bupivacaine is preferred in prolonged surgical procedures with its long duration of action and residual analgesic effect. The aim of this study was to evaluate the anesthetic, analgesic, hemodynamic effects of 4% articaine and 0.5% bupivacaine in extraction of impacted mandibular third molar teeth in intraoperative and postoperative periods. Hemodynamic parameters, onset of anesthetic action, total amount, intraoperative comfort, intraoperative bleeding, duration of postoperative anesthesia and analgesia, rescue analgesic use, maximum incisal opening and postoperative pain at 6th, 12th, 24th, 48th and 72th hours and 7th day using a visual analogue scale be evaluated.

NCT ID: NCT04534426 Completed - Clinical trials for Impacted Third Molar Tooth

Topical Arnica and Mucopolysaccharide Polysulfate on Postoperative Pain, Edema and Trismus

Start date: December 1, 2018
Phase: Phase 4
Study type: Interventional

The present study was to evaluate the effect of topical Arnica and MPSP application with respect to visual analogue scale (VAS) scores, maximal interincisal opening (MIO) and edema values after mandibular impacted third molar removal on days 1, 3, 5 and 10 postoperatively. The following null hypotheses of the present research were determined as follows: usage of topical agents would not influence i) VAS scores, ii) MIO values, and iii) edema values on 1st, 3rd, 5th, and 10th days after the mandibular impacted third molar surgery

NCT ID: NCT04427683 Completed - Mental Health Issue Clinical Trials

Effects of a Brief Mindful Parenting Program for Hong Kong Chinese Impacted by Social Unrest

MPHKC
Start date: May 15, 2020
Phase: N/A
Study type: Interventional

A four session mindful parenting workshop is designed to promote parental mental health during the social unrest in 2020. This study is conducted to investigate the outcome of the program. It is a randomised control trial design and will be conducted in five sites in Hong Kong. An estimated 340 parents will be recruited and randomised into an intervention group and a wait-list control group. The primary outcome is parental depression. Secondary outcomes include parental anxiety and post-traumatic stress, negative emotions, family functioning, family conflict and mindful parenting. Exposure to social unrest will be measured and the relationship to mental health and effects of the program will be examined.

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.