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NCT ID: NCT03589235 Recruiting - Gingival Recession Clinical Trials

Platelet-Rich Fibrin Dressing in the Management of Free Gingival Graft

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Evaluation of two dressing materials; a Platelet-Rich Fibrin (PRF) dressing and a non-eugenol-based (Coe-Pakā„¢) dressing in the management of free gingival graft and donor site palatal wound.

NCT ID: NCT03428282 Active, not recruiting - Clinical trials for Inferior Alveolar Nerve Block

Pain and Anxiety Control During Traditional Mandibular Anesthesia in Children Using Distracting Tools

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effectiveness of two different audiovisual distraction techniques (Audio Video eyeglasses "VR BOX"/ Tablet) in the management of anxious pediatric patients during inferior alveolar nerve block Group A (Control group): IAN will be administrated with basic behavior guidance techniques and without using any type of distraction aids. Group B: IAN will be administrated with using AV eyeglasses "VR BOX" and wireless headphone. Group C: IAN will be administrated with using tablet device and wireless headphone All of the children who experienced an inferior alveolar block with/without distraction will be assessed by using a combination of measures: Wong-Baker FACES (self-report), pulse rate (physiological) and behavior (using FLACC behavior rating scale "external evaluator

NCT ID: NCT03400111 Recruiting - Clinical trials for Orthodontic Appliance Complication

The Role of Paracetamol-caffeine and Laser Irradiation on Controlling Pain and Discomfort During Orthodontic Treatment

Start date: September 15, 2017
Phase: N/A
Study type: Interventional

Patients with class I malocclusion who have mild to moderate crowding will be treated in this study. The efficacy of low level laser therapy and Panadol-extra® in relieving pain due to orthodontic treatment will be assessed. The effect of these two interventions on oral-health related quality of life during all stages of orthodontic treatment will be explored, i.e. at the following stages: (1) separation between teeth, (2) archwire changing, (3) bonding of brackets, (4) removal of the fixed appliances. There are three groups : 1. a group of patient being irradiated with low-level laser therapy (LLLT) at specific time points to relieve pain and discomfort. 2. a group of patient in which pain control will be accomplished by prescribing Panadol Extra tablets in a regular manner. 3. a group of patients in which nothing will be given to them during the course of treatment.

NCT ID: NCT03399760 Recruiting - Clinical trials for Malocclusion, Angle Class II, Division 1

Efficacy of Injectable Platelet Rich Fibrin (i-PRF) in Enhancing Bone Quality

Start date: August 20, 2017
Phase: N/A
Study type: Interventional

Twenty patients need therapeutic extraction of the maxillary first premolars with subsequent retraction of the maxillary canines, will be divided randomly into two groups, and will randomly assigned to one side of the maxillary arch at the first premolar region, and the other side served as the control. Canine retraction will be initiated after completion of the leveling and alignment phase via closed nickel-titanium coil springs applying 150 g of force per side. Soldered transpalatal arch will be used as an anchor unit. The dento-alveolar changes will be assessed immediately before retraction and after 6 months using CBCT.

NCT ID: NCT03399422 Recruiting - Clinical trials for Malocclusion, Angle Class II, Division 1

Efficacy of Biological Technique in Upper Canine Retraction and Levels of Discomfort

Start date: August 20, 2017
Phase: N/A
Study type: Interventional

Twenty patients need therapeutic extraction of the maxillary first premolars with subsequent retraction of the maxillary canines, will be divided randomly into two groups, and will randomly assigned to one side of the maxillary arch at the first premolar region , and the other side served as the control. canine retraction will be initiated after completion of the leveling and alignment phase via closed nickel-titanium coil springs applying 150 g of force per side , soldered transpalatal arch will be used as an anchor unit. Pre- and post distalization dental casts will be evaluated to study rate of canine distalization, over a follow-up period until a Class I canine relationship will be achieved. The levels of Pain and discomfort will be monitored using a questionnaire with a VAS scale administered three times during the first day after prf injection.

NCT ID: NCT03391947 Recruiting - Gingival Recession Clinical Trials

Semilunar and Conventional Coronally Positioned Flap for the Treatment Gingival Recession

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

A clinical evaluation of using the semilunar coronally position flap (SCPF) compared to the conventional coronally advanced flap (CAF) with modification to treat class I Miller gingival recession. The coronally repositioned gingival margin will be stabilized by coronally anchored suture with composite stops on the buccal surface of the tooth using flowable composite. The sample size will be ten patients. Each patient has bilateral Miller Class I gingival recessions; one will be treated with SCPF, while the other will be treated with CAF

NCT ID: NCT03388957 Recruiting - Extrusion of Tooth Clinical Trials

Oral Propranolol for Reducing Pediatric Dental Patients Anxiety

Start date: September 30, 2017
Phase: N/A
Study type: Interventional

Evaluating anxiety, behavior, sedation and vital signs during dental extraction after orally taking either propranolol, midazolam, a combination of both or placebo in 6-9 years old uncooperative patients.

NCT ID: NCT03354442 Active, not recruiting - Clinical trials for Malocclusion, Angle Class III

Treatment of Class III Malocclusion Using Modified Fixed Mandibular Retractor Appliance

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

This experimental study aims to evaluate the efficiency of the Modified Fixed Mandibular Retractor Appliance in the treatment of skeletal class III malocclusion. The study sample will consist of 44 patients with skeletal class III malocclusion. The sample will be allocated randomly into two groups: experimental group and untreated control group. The soft and hard tissue changes will be assessed using lateral cephalometric radiographs before the treatment and after obtaining 3mm positive overjet.

NCT ID: NCT03310086 Active, not recruiting - Crowding, Tooth Clinical Trials

Acceleration of Lower Anterior Teeth Leveling and Alignment Using Corticision

Start date: January 2017
Phase: N/A
Study type: Interventional

This experimental study will evaluate the effect of corticision on accelerating the leveling and alignment of lower crowded incisors compared with the control untreated group using cone beam computed tomography. The study sample will consist of 26 patients with less than 6 mm crowding. The sample will be allocated randomly into two experimental groups. The brackets and passive SS wire will be applied with radiographic metal guides between each tooth to allow for accurate corticision site 2 mm below the gingival papilla and to prevent tooth roots injury. The dentoalveolar changes occurring after leveling and alignment of lower anterior teeth will be evaluated using CBCT radiographs, Frequency, degree of root resorption, and the incidence of bone dehiscence will be assessed in relation to initial situation.

NCT ID: NCT03305679 Active, not recruiting - Clinical trials for Implant Site Reaction

Clinical Efficacy of the Immediate Implant Loading

Start date: January 19, 2017
Phase: N/A
Study type: Interventional

Aim: The aim of this study to Assess the healing process of the immediate implant loading with two different provisional techniques (direct and indirect). Materials and methods: 20 implant in the aesthetic zone either in the incisor or in the canine area and excluding the lateral location and then immediate loading is achieved for the 20 implants (10 for direct and 10 for indirect method) Clinical Aspect :color change , healing and bone resorption Esthetic assessment and patient acceptance will be assessed using specific tools. Lab aspect: surface roughness and Marginal fit will be measured to have clue vision.