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Prognathism clinical trials

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NCT ID: NCT06402656 Not yet recruiting - Clinical trials for Malocclusion, Angle Class III

Comparison of Customized and Standard Facemasks for Early Treatment of Class III Malocclusion

Start date: May 6, 2024
Phase: N/A
Study type: Interventional

The aim of the study is to compare a customized facemask for the treatment of Class III malocclusion in the prepubertal growing patient (patients between the ages of 5 and 12 years) versus a standard commercial facemask. Specifically, preference, pain, difficulty in sleeping, time of use, and possible complications for the two types of facemasks will be analyzed. This is a single-center, national, controlled, superiority, randomized, crossover, open-label study. Each patient will be treated with both the customized facemask and the standard commercial facemask. Each patient will wear one type of facemask for 2 months and the other type of facemask for the next 2 months. After 2 weeks and at the end of therapy with each of the facemask types, the patient, with the possible help of the parents, will have to answer a questionnaire about pain and difficulty sleeping and report any complications. In addition, after completing both phases (fourth month), the patient should indicate a preference for one of the two types of mask with which to complete therapy for an additional 6 months.

NCT ID: NCT06379152 Recruiting - Clinical trials for Heart Failure With Preserved Ejection Fraction

Effect of Bilirubin on Prognosis in Heart Failure With Preserved Ejection Fraction

Start date: September 20, 2020
Phase:
Study type: Observational

Factors influencing the prognosis of patients with heart failure with preserved ejection fraction (HFpEF) have been extensively studied. Previous studies have found that elevated serum total bilirubin levels are associated with cardiac death, heart failure readmission, and all-cause mortality in patients with chronic heart failure. However, the relationship between direct bilirubin and prognosis in patients with HFpEF is unclear.

NCT ID: NCT06366737 Not yet recruiting - Clinical trials for Maxillary Prognathism

En-mass Retraction by Lingual Retractor Versus Clear Aligner Appliances

Start date: April 2024
Phase: N/A
Study type: Interventional

en-mass retraction by lingual retractor versus clear alighner therapy

NCT ID: NCT06250127 Recruiting - Jaw Protrusions Clinical Trials

The Effectiveness of Modified 3D Printed Customized Facemask Appliance for Treatment of Class III Malocclusion

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

A randomized clinical trial to introduce a modified 3D printed customized maxillary protraction facemask and evaluate its efficacy in comparison with the conventional maxillary protraction facemask therapy in correction of Class III malocclusion of young patients

NCT ID: NCT06244563 Completed - Clinical trials for Malocclusion, Angle Class III

Evaluation of Different Anchorage-supported Appliances and Expansion Procedures for Face Mask Treatment

Start date: June 8, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to assess and compare the effect of two appliances (Hybrid-Hyrax expander/ Bonded rapid maxillary expander (RME)) supported by different anchorage units and two different expansion procedures (routine rapid maxillary expansion protocol (routine)/ alternative rapid expansion and constriction protocol (alt-RAMEC)) on maxillary protraction during face mask (FM) treatment.

NCT ID: NCT05913076 Completed - Clinical trials for Maxillary Retrognathism

Class III Malocclusion and ALT-RAMEC

Start date: January 13, 2012
Phase: N/A
Study type: Interventional

Diverse viewpoints exist regarding the correlation between the conventional rapid maxillary expansion (RME) and facemask approach and the alternative RME and facemask hybrid technique (Alt-RAMEC) in terms of the degree of maxillary protraction. The findings of the study may offer a novel approach to protocol selection based on the anomaly's degree of severity. The objective of this investigation is to assess and contrast the skeletal and dentoalveolar outcomes of three distinct Alt-RAMEC techniques.

NCT ID: NCT05822271 Recruiting - Clinical trials for Malocclusion, Angle Class III

Evaluation of Surgical Outcomes of Patients Treated With the Surgery First Approach and Aligners

Start date: January 30, 2022
Phase: N/A
Study type: Interventional

The purpose of this prospective study is to compare treatment outcomes and the quality of life of skeletal Class III patients treated with conventional fixed appliances and aligners undergoing Surgery-first approach. Data will be collected through validated questionnaires: OQLQ (Orthognathic Quality of Life Questionnaire), OHIP-14 (Oral Health Impact Proļ¬le), SF-36 (Medical Outcomes Study 36 - Item Short-Form Health Survey) and IOTN (Index of Orthodontic Treatment Need).

NCT ID: NCT05713084 Active, not recruiting - Clinical trials for Maxillofacial Abnormalities

Condylar Position Changes and TMJ Functions After BSSO Mandibular Setback, Low Medial Cut.

Start date: September 28, 2022
Phase: N/A
Study type: Interventional

This study hypotheses that using low medial cut osteotomy BSSO in mandibular setback can be an efficient and effective method to limit the bony segment interferences , decreasing muscles stripping during osteotomy ,decrease condylar torque and so securing preoperative condylar position during BSSO in comparison with using high medial cut BSSO.

NCT ID: NCT05536596 Not yet recruiting - Clinical trials for Orthognathic Surgery

Pharmacological Treatment on the Recovery of Neurosensory Disturbance After Bilateral Sagittal Split Osteotomy

Start date: September 30, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

The bilateral sagittal split osteotomy (BSSO) of the mandible is one of the most used surgical techniques to achieve a harmonious jaw relation in the context of orthognathic surgery. Nevertheless, one of its main complications is neurosensory damage to the inferior alveolar nerve, which can cause severe impact in the quality of life on patients who suffer from it permanently. The purpose of this randomized clinical trial is to provide rigorous scientific evidence of the pharmacological effect of 1) Melatonin, 2) combination uridine triphosphate (UTP), cytidine monophosphate (CMP), and hydroxycobalamin (UTP/CMP/hydroxycobalamin) and 3) hydroxycobalamin regarding neurosensory disturbances incidence and persistence after BSSO.

NCT ID: NCT05475548 Enrolling by invitation - Clinical trials for Effect of PowerScope Appliance in Treatment of Patients With Class 3 Malocclusion

Effect of Skeletally Anchored Reversed PowerScope Appliance in Orthodontic Treatment of Patients With Class III Malocclusion

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

the PowerScope appliance is found to be efficient for the treatment of class II malocclusion. Accordingly, it appears valuable to investigate the efficiency of skeletally anchored powerScope in the treatment of class III malocclusion