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Tooth, Impacted clinical trials

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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: NCT05484401 Completed - Tooth Diseases Clinical Trials

Ibuprofen Liquid Capsules 2 x 200 mg Efficacy and PK/PD Study in Surgical Removal of Impacted Third Molars

Start date: August 9, 2022
Phase: Phase 3
Study type: Interventional

This is a single centre, three-arm randomised, double-blind, double-dummy, parallel group, single-dose, active and placebo-controlled efficacy and pharmacokinetics/ pharmacodynamics study to evaluate the efficacy and safety of 2 x 200 mg Ibuprofen Liquid Capsules in subjects with post-operative dental pain.

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: NCT05318846 Completed - Pain Clinical Trials

A Study to Evaluate the Efficacy and Safety of HRS4800 Tablets for Postoperative Analgesia After Impacted Teeth Removal Surgery.

Start date: January 14, 2022
Phase: Phase 2
Study type: Interventional

The study is being conducted to evaluate the efficacy and safety of HRS4800 tablets for postoperative analgesia after impacted teeth removal surgery.

NCT ID: NCT05296902 Completed - Tooth, Impacted Clinical Trials

Performance of Safety of SILKAM® Suture Material in Oral Surgery

SILKOS
Start date: September 21, 2022
Phase:
Study type: Observational

Assessment of SILKAM® suture material in mucosal closure in oral surgery (mucosal sutures). A prospective, monocentric, single arm observational study.

NCT ID: NCT05170516 Completed - Clinical trials for Impacted Third Molar Tooth

The Effect of Saline Irrigation at Different Temperatures on Pain, Edema, and Trismus After Impacted Third Molar Surgery

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

Third molar surgery is one of the most common procedures in oral surgery and the most common postoperative complications are swelling, pain, and trismus. This study aims to evaluate the postoperative morbidity (pain, swelling, and trismus) in third molar surgery performed using different degrees of cooled and room temperature irrigation solutions.

NCT ID: NCT05126264 Completed - Pain Clinical Trials

Efficacy of Chronoterapy in Oral Surgery

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

Lower third molar extraction is one of the most common treatments in oral surgery practice. It is a treatment with inherent complications such as postoperative pain, swelling or trismus. In order to minimize disconfort after extraction, analgesic and anti-inflammatory medication is prescribed. Recently, it is seen that circadian rhythm may play an important role on drugs metabolism, modulating its effect depending on the moment of administration. The aim of the study is to analyze if dosage modification of a Non Steroideal Anti-Inflammatory (ibuprofen) affects on postoperative pain, swelling and open mouth limitation comparing to the normal dosage.

NCT ID: NCT04989127 Completed - Clinical trials for Impacted Wisdom Tooth

Comparison The Postoperative Effects of Local and Systemic Antibiotics Applied With Platelets Rich Fibrin

Start date: March 17, 2019
Phase:
Study type: Observational

The aim of this study was investigate the comparison of postoperative effects of local antibiotics mixed with platelet-rich fibrin and postoperative systemic antibiotic applications prescribed for mandibular impacted third molar tooth extraction. The study included a total of 75 patients with impacted mandibular third molar. Patients were evaluated in 5 randomly separated groups. For the first and third group, Platelets Rich Fibrin+ systemic Antibiotics were applied into the tooth socket and for the second and fourth group, Platelets Rich Fibrin + local antibiotics were applied, respectively. There was a control group which only Platelets Rich Fibrin was applied into the socket. The outcome variables were pain, swelling, the number of analgesics taken, and trismus. These variables were also assessed based on first, second, third, and seventh days following the operation.

NCT ID: NCT04889781 Completed - Clinical trials for Impacted Mandibular Third Molar Extraction

Piezo-surgery Technique and Intramuscular Dexamethasone Injection to Reduce Postoperative Pain After Impacted Mandibular Third Molar Surgery

Start date: February 1, 2019
Phase: Phase 4
Study type: Interventional

The purpose of my study is to test the effect of using piezosurgery and dexamethasone injection in the surgical extraction of impacted mandibular third molars, on Postoperative Pain.

NCT ID: NCT04860388 Completed - Clinical trials for Orthodontic Treatment

Gingival Thickness of Impacted Maxillary Canines

Start date: May 29, 2019
Phase: N/A
Study type: Interventional

This study was conducted to compare the periodontal health of labially and palatally impacted maxillary canines with similar mesio-distal displacement, perpendicular distance, and angulation, and to compare them with the contralateral canines that served as control teeth. Two null hypothesis were tested: (1) there are no differences in attached and keratinized gingival widths and gingival thickness between impacted teeth and controls, and (2) there are no differences in attached and keratinized gingival widths and gingival thickness of labially and palatally impacted canines.