Clinical Trials for Facial Injuries and Disorders

Currently registered clinical trials for Facial Injuries and Disorders from ClinicalTrials.gov. 13 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Facial Injuries and Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 13
  • Active, not recruiting: 6
  • Completed: 22
  • Other: 9

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT04634383 — A Phase I Feasibility Study of an Intracortical Visual Prosthesis (ICVP) for People With Blindness

StatusRecruiting
PhaseN/A
SponsorIllinois Institute of Technology
Enrollment5
Study TypeINTERVENTIONAL
ConditionsOcular Injury; Optic Nerve Diseases; Photoreceptor Degeneration; Blindness,Acquired
Interventions

The purpose of this study is to determine the feasibility of producing artificial vision in persons with blindness. Study participants will have wireless electrical stimulators implanted into the cortical vision processing areas of their brains. The ability of the participants to perceive artificial vision in response to electrical stimulation will be assessed.

NCT06724029 — Neurosurgical Outcome Network

StatusRecruiting
PhaseN/A
SponsorFondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
Enrollment4500
Study TypeOBSERVATIONAL
ConditionsAneurysms; Arteriovenous Malformations; Cavernomas; Skull Base Tumors; Moyamoya Disease

The evaluation of neurosurgical outcomes varies from center to center, and the predictive factors that determine these outcomes are not fully known or shared. This study aims to assess outcomes and their predictors using measures agreed upon by the participating centers. Standardizing the evaluation of outcomes and predictors improves the quality of research, allows for data comparison, and fac…

NCT06257355 — Study to Evaluate the Safety and Efficacy of CSB-001 Ophthalmic Solution 0.1% in Subjects With Corneal Scars

StatusRecruiting
PhasePhase 1
SponsorClaris Biotherapeutics, Inc.
Enrollment20
Study TypeINTERVENTIONAL
ConditionsCorneal Scar
Interventions

This study will enroll subjects with recently formed corneal scars that resulted from a corneal insult presenting and diagnosed within the past approximately 30 days and not less than approximately 7 days. All subjects will be assigned to CSB-001 investigational treatment on Day 1. All subjects will dose with CSB-001 four times daily or three times daily starting on Day 1 and continue until Day…

NCT06429501 — Local Anesthesia for Facial Fractures

StatusRecruiting
PhasePhase 2
SponsorWashington University School of Medicine
Enrollment70
Study TypeINTERVENTIONAL
ConditionsPain Management
Interventions;

The study is a double-blind randomized, placebo controlled trial examining the impact of perioperative bupivacaine nerve block on PACU recovery metrics. Patients with operative facial fractures are randomized to receive either bupivacaine or saline injections prior to the anesthesia emergence.

NCT07557875 — Healing Efficacy of Diode Laser in Lingual Frenectomy

StatusRecruiting
PhaseN/A
SponsorUniversity of Medicine and Pharmacy at Ho Chi Minh City
Enrollment53
Study TypeINTERVENTIONAL
ConditionsAnkyloglossia; Tongue-tie
Interventions;

This study aims to compare the wound healing efficacy and postoperative experiences between the 940 nm diode laser technique and the traditional electrosurgery method for treating ankyloglossia (tongue-tie) in children aged 3 to 6 years.

Participants are randomly assigned to one of two groups: Experimental Group - Patients undergo lingual frenectomy using a 940 nm diode laser and Active Compar…

NCT05964140 — The MANTRA Trial (MANdibular TRauma and Antibiotic Use)

StatusRecruiting
PhasePhase 3
SponsorEast Lancashire Hospitals NHS Trust
Enrollment2841
Study TypeINTERVENTIONAL
ConditionsMandible Fracture; Post-operative Antibiotics
Interventions
  1. FULL TITLE OF THE PROJECT Should we use post-operative antibiotics following surgery for patients with mandible fractures? The MANTRA trial (MANdibular TRauma and Antibiotic use)
  2. SUMMARY OF RESEARCH (ABSTRACT) Research Question: Are post-operative antibiotics required following surgery for patients with mandible fractures? Background: Mandible fractures are the commonest facial fractures …

NCT07016750 — A Study Comparing KB803 and Matched Placebo in Patients With Dystrophic Epidermolysis Bullosa

StatusRecruiting
PhasePhase 3
SponsorKrystal Biotech, Inc.
Enrollment16
Study TypeINTERVENTIONAL
ConditionsDystrophic Epidermolysis Bullosa; DEB - Dystrophic Epidermolysis Bullosa; Recessive Dystrophic Epidermolysis Bullosa; Dominant Dystrophic Epidermolysis Bullosa
Interventions;

KB803-EYE-01 is a Phase 3 double-blind, randomized, placebo-controlled, crossover study to evaluate the safety and efficacy of KB803 versus matched placebo in pediatric and adult subjects with recurrent corneal abrasions due to dystrophic epidermolysis bullosa (DEB).

NCT06618703 — Brain Irradiation for Childhood Cancer - Endocrine Monitoring During the First Years

StatusRecruiting
PhaseN/A
SponsorUniversity Hospital, Angers
Enrollment230
Study TypeINTERVENTIONAL
ConditionsEndocrine; Deficiency; Hypothalamo-Pituitary Disorder; Radiotherapy Side Effect
Interventions

BICHE- 1: Brain Irradiation for Childhood cancer - Endocrine monitoring during the first five years is a study of endocrine monitoring after cerebral radiotherapy.

The study concerns patients in remission at the end of oncological treatment aged between 4 and 18 years at the time of inclusion and who have had radiotherapy before the age of 16, irradiating all or part of the brain, with a delay…

NCT06596733 — Vit-A-Vision® Clinical Investigation

StatusRecruiting
PhaseN/A
SponsorOmniVision GmbH
Enrollment77
Study TypeINTERVENTIONAL
ConditionsBurning Eye; Irritation; Eyeball; Tired Eye; Dry Eye Disease
Interventions

Symptoms of ocular discomfort include dryness, burning, stinging, photophobia, foreign body sensation and contact lens intolerance. These symptoms may affect basic daily activities, such as reading, driving, and working with computers. In case of moderate to severe conditions, dry eye disease is also associated with significant pain. Dry eye disease (DED) affects hundreds of millions of people …

NCT07263893 — Inter Flex Three Dimensional Plate in Management of Mandibular Fracture RCT

StatusRecruiting
PhaseN/A
SponsorSuez Canal University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsMandibular Fracture Treatment
Interventions

The goal of this clinical trial is to learn if The use of a 3D-designed Inter-flex plate will achieve safe and desirable anatomical & functional restoration with reduced operative time in mandibular fracture,

  • Improvement of occlusal and inter-cuspal relation in addition to stabilized intra-fragmentary mobility,
  • Offer greatest resistance to displacement
  • shows most favorable biomechanical…

NCT07208799 — Comparison of Submucosal Dexamethasone and Methylprednisolone in Postoperative Sequelae of Parasymphsis Fractures

StatusRecruiting
PhasePhase 2
SponsorNishtar Medical University
Enrollment72
Study TypeINTERVENTIONAL
ConditionsMandible Fracture; Edema Face; Pain Management; Corticosteroid Injection
Interventions;

The rationale of the current research is to address the limitation of existing knowledge as it is not clear which of the two drugs (Dexamethasone or Methylprednisolone) is more effective in reduction of postoperative sequelae in patient with mandibular parasymphysis fracture. This study fills the gap by providing sound evidence on the preferred steroid option to help clinicians have more data t…

NCT07449000 — Losartan for Corneal Fibrosis

StatusRecruiting
PhaseN/A
SponsorUniversidad Autonoma de Nuevo Leon
Enrollment46
Study TypeINTERVENTIONAL
ConditionsCorneal Scarring Fibrosis
Interventions;

This is a prospective, randomized, double-blinded, controlled clinical trial designed to evaluate the efficacy and safety of topical losartan in improving visual acuity, contrast sensitivity and reducing corneal densitometry, corneal aberrations and corneal scarring severity in adult patients with corneal scars of different etiologies. Participants will be randomly assigned to receive either to…

NCT07560631 — SeeMe: Using Automated Facial Tracking to Detect Voluntary Behavior in Brain Injury

StatusRecruiting
PhaseN/A
SponsorStony Brook University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsTraumatic Brain Injury (TBI) Patients; Severe Traumatic Brain Injury
Interventions

Objective: This prospective interventional study introduces “SeeMe,” an automated, high-resolution computer vision platform designed to objectively quantify microscopic, auditory command-evoked movements in patients with Traumatic Brain Injury (TBI). Current clinical assessments, such as the Glasgow Coma Scale (GCS) and Coma Recovery Scale-Revised (CRS-R), rely on subjective human observation a…

Active, Not Recruiting

NCT03887988 — Orbital Fractures Registry

StatusActive, not recruiting
PhaseN/A
SponsorAO Innovation Translation Center
Enrollment300
Study TypeOBSERVATIONAL
ConditionsOrbital Fractures; Blow Out Fracture of Orbit
Interventions; ;

Approximately 300 patients presenting orbital blow-out fracture will be enrolled prospectively in this registry. All patients, surgically and nonsurgically treated as per standard (routine) of care will be followed-up (FU) within the registry for a period of 6 months.

NCT05593237 — Transcranial Magnetic Stimulation for Chronic Neuropathic Pain

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of California, San Francisco
Enrollment32
Study TypeINTERVENTIONAL
ConditionsChronic Neuropathic Pain; Post-Stroke Pain; Trigeminal Neuralgia; Nerve Injury; Spinal Cord Injuries
Interventions;

Chronic neuropathic pain is defined as pain caused by a lesion or disease of the somatosensory nervous system. It is highly prevalent, debilitating, and challenging to treat. Current available treatments have low efficacy, high side effect burden, and are prone to misuse and dependence. Emerging evidence suggests that the transition from acute to chronic neuropathic pain is associated with reor…

NCT05742932 — Prospective Study to Evaluate the Performance and the Safety of Global D’s Implants of Craniomaxillofacial Surgery (CMF) Ranges Indicated for Trauma Surgery (CMF-TRAUMA)

StatusActive, not recruiting
PhaseN/A
SponsorGlobal D
Enrollment99
Study TypeOBSERVATIONAL
ConditionsTrauma Injury; Maxilla Fracture; Maxillofacial Trauma
Interventions

This study is set up within the framework of the European Union regulation 2017/745 on medical devices. Its objective is to confirm the performance and safety of the Global D implants (ORTRAUTEK® and MINITEK/MICROTEK®) used for trauma surgery.

NCT07245810 — Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up

StatusActive, not recruiting
PhaseN/A
SponsorStryker Craniomaxillofacial
Enrollment726
Study TypeOBSERVATIONAL
ConditionsMandibular Fractures; Facial Fracture; Maxilla Fracture; Orthognathic Surgical Procedures
Interventions

A retrospective post market follow up to confirm safety and performance of Stryker’s Facial iD Universal Plate Configurator (UPC) implants in the clinical setting. The study is performed to confirm the product’s performance and safety by systematically collecting clinical data on its use.

NCT07574554 — Fixation of Mandibular Angle Fracture Using 3D Titanium Miniplate Versus Standard Two Plate Fixation

StatusActive, not recruiting
PhaseN/A
SponsorCairo University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsMandible Fracture; Force Measurement
Interventions;

Hypothesis The investigators hypothesis that fixation of mandibular angle fractures using a 3D titanium miniplate will provide better occlusal bite force than intraoral fixation using the standard two-plate technique.

The investigators expect that this method will facilitate a faster recovery time for participants to regain baseline occlusion force.

NCT07340528 — Endoscopically Assisted Management of Maxillofacial Fractures: A Prospective Study on Efficacy and Outcomes

StatusActive, not recruiting
PhaseN/A
SponsorSohag University
Enrollment30
Study TypeINTERVENTIONAL
ConditionsMaxillofacial Injuries; Maxillofacial Trauma; Subcondylar Process of Mandible Closed Fracture; Orbital Floor (Blow-Out) Closed Fracture; Frontal Sinus Fracture
Interventions

The goal of this clinical trial is to assess the efficacy of endoscopically assisted management of maxillofacial fractures in terms of fracture reduction, stability, and functional outcomes.

Not Yet Recruiting

NCT07461324 — Surgeons’ Prediction of Dental Surgery Complications and the Influence of Patient Characteristics: Development of an AI Model

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Copenhagen
Enrollment3000
Study TypeOBSERVATIONAL
ConditionsPostoperative Infections; Mandibular Nerve Injuries; Alveolar Osteitis; Complication; Dental Implantation

The goal of this observational study is to learn how to better predict and prevent intra- and postoperative complications in oral surgery in adult patients referred for oral surgical procedures. The study aims to understand how accurately surgeons can foresee complications and which patient, tooth, and surgery related factors influence the outcomes.

The research questions are:

  • What is the i…

NCT06978530 — 3D Custom Plate vs. Standard Titanium Plates for Mandibular Sub-condylar Fractures Fixation

StatusNot yet recruiting
PhaseN/A
SponsorEsraa Mosad Tawfik
Enrollment30
Study TypeINTERVENTIONAL
ConditionsMandibular Sub-condylar Fracture
Interventions;

This randomized clinical trial aims to conduct a comprehensive clinical and radiographic evaluation by comparing the efficacy of standard titanium fixation plates with three dimensional custom plate in the management of sub-condylar fractures. By assessing the clinical outcomes, accuracy of reduction of the fracture segments, and bite force promoted by both fixation modalities.

NCT07225699 — IN PATIENTS WITH CORNEAL ABRASIONS TREATED WITH COLLAGEN CORNEAL SHIELDS IN THE EMERGENCY DEPARTMENT SETTING

StatusNot yet recruiting
PhaseN/A
SponsorMilton S. Hershey Medical Center
Enrollment60
Study TypeINTERVENTIONAL
ConditionsCorneal Abrasions
Interventions;

This is a single-center, double-arm, patient masked, randomized controlled trial. Subjects will be enrolled in the Emergency Department at the Penn State Milton S. Hershey Medical Center. Eligible subjects must present to the ED and be diagnosed with a traumatic corneal abrasion. One eye from each patient will be considered the study eye.

NCT07562594 — Eyelid Taping Alone Versus Taping With Lubricant Eye Drops for Perioperative Corneal Protection

StatusNot yet recruiting
PhaseN/A
SponsorFatih Sultan Mehmet Training and Research Hospital
Enrollment200
Study TypeINTERVENTIONAL
ConditionsCorneal Injury; Exposure Keratopathy; Perioperative Complications
Interventions;

During general anesthesia, the eye’s natural protective reflexes are suppressed, which can lead to corneal drying and injury. To prevent this, anesthesiologists routinely tape the eyelids closed. In many centers, lubricant eye drops are also applied in addition to taping, but whether this adds meaningful protection is unclear.This study will compare two approaches to eye protection during gener…

NCT07671183 — Effect of Adipose Tissue Derived Autologous Mesenchymal Stem Cell Concentrate on Bone Quality in Mandibular Fracture Healing.

StatusNot yet recruiting
PhaseN/A
SponsorCairo University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsMandible Fracture
Interventions;
  • The goal of study is to evaluate the effectiveness of adipose tissue derived-MSCs concentrate application in mandibular fractures. The main question it aims to answer is: Does intervention enhance bone quality, reduce complications and reduce bone regeneration time.
  • Researchers will compare the effectiveness of adipose tissue derived-MSCs concentrate application with ORIF to ORIF alone to s…

NCT07240649 — Emerging Indications for Hyperbaric Oxygen Treatment

StatusNot yet recruiting
PhasePhase 4
SponsorJay C. Buckey Jr.
Enrollment100
Study TypeINTERVENTIONAL
ConditionsPost-COVID-19 Condition; Ulcerative Colitis; Crohn Disease; Calciphylaxis; Frostbite
Interventions;

This study will evaluate the effectiveness of hyperbaric oxygen therapy (HBOT) on treating emerging indications (i.e., conditions that have shown to potentially benefit from HBOT) using the Multicenter Registry for Hyperbaric Oxygen Treatment. The study team aims to collect ongoing data on how well HBOT treats these emerging indications, and to add these data to the growing HBO Registry. The re…

Enrolling by Invitation

NCT07608380 — Accuracy of Positioning Guide and Customized Plate in Zygomaticomaxillary Complex Fractures

StatusEnrolling by invitation
PhaseN/A
SponsorCairo University
Enrollment8
Study TypeINTERVENTIONAL
ConditionsZygomaticomaxillary Complex Fracture; Zygoma Fracture; Zygomatic Fractures
Interventions;

The goal of this clinical trial is to evaluate the accuracy and stability of positioning guides and customized titanium plates in the treatment of Zygomaticomaxillary Complex (ZMC) fractures. The main questions it aims to answer are:

  • Is the anatomical reduction achieved using a virtual planning-based positioning guide accurate when compared to preoperative plans?
  • Does the customized titani…

NCT07057284 — DENTOFACIAL-PBT Stage 2 - Feasibility Study

StatusEnrolling by invitation
PhaseN/A
SponsorManchester University NHS Foundation Trust
Enrollment255
Study TypeOBSERVATIONAL
ConditionsHead and Neck Cancer; Radiotherapy Side Effect; Adverse Effect of Radiation Therapy; Childhood Cancer; Dental Developmental Disorders and Anomalies
Interventions

What is the health problem? Proton beam therapy (PBT), a type of radiotherapy treatment, can be especially beneficial to children and teenagers with cancer. PBT works by damaging cancer cells, but it can also damage healthy parts of the body nearby. This can include the teeth and jaws if the cancer is in the head and neck region. Unfortunately, the investigators do not yet fully understand the …

Completed Trials

NCT03423277 — Easy Stretch Toolkit: A Pilot Study

StatusCompleted
PhaseN/A
SponsorThe University of Texas Medical Branch, Galveston
Enrollment8
Study TypeINTERVENTIONAL
ConditionsFacial Injuries
Interventions

To research the use of a novel set of intraoral tools called the Easy Stretch Toolkit for the therapeutic management of facial burns and other facial disorders.

NCT07340879 — Reconstruction of Orbital Floor Blow-out Fractures by Titanium Mesh Versus Autogenous Iliac Graft

StatusCompleted
PhaseN/A
SponsorAssiut University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsBlow-Out Fractures
Interventions;

Blow-out fractures result from direct blunt impacts to the orbit which causes an immediate rise increase in intra-orbital pressure. Decompression via fracture of the orbital floor then occurs. Motor vehicle accidents are the main cause of orbital trauma. Also, industrial accidents, sports-related facial trauma, and assaults are important causes.

Clinical manifestations include ecchymosis, limi…

NCT05271383 — Study Evaluating the Performance and Safety of Global D Implants Indicated for Orthognathic Surgery

StatusCompleted
PhaseN/A
SponsorGlobal D
Enrollment198
Study TypeOBSERVATIONAL
ConditionsOrthognathic Surgery; Maxillofacial Abnormalities; Maxilla Fracture
Interventions

This study is set up within the framework of the European Union regulation 2017/745 on medical devices. Its objective is to confirm the performance and safety of the Global D implants (ORTRAUTEK® and MINITEK®) used for orthognathic surgery.

NCT07520227 — Comparative Evaluation of 3D-printed (PEEK) Plates Versus Titanium 3D Plate for Fracture Fixation at the Mandibular Angle

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment22
Study TypeINTERVENTIONAL
ConditionsFracture Mandible
Interventions;

Is patient specific customized computer assisted 3D PEEK plates more superior to 3D titanium plate in fixation of mandibular angle fractures?

NCT06003504 — The Impact of First Aid Blended Learning Training on Learning Outcomes and Helping Behaviour of Adult Laypeople in Rwanda

StatusCompleted
PhaseN/A
SponsorCentre for Evidence-Based Practice, Belgium
Enrollment540
Study TypeINTERVENTIONAL
ConditionsEmergencies; Injuries; Illness Physical
Interventions;

The goal of this study is to assess the impact of a first aid training delivered through a blended learning approach on learning outcomes and helping behaviour in adult laypeople in Rwanda.

Participants will be randomly assigned to either:

  • a first aid training with blended learning approach;
  • a first aid training with conventional face-to-face approach;
  • no first aid training.

All partic…

NCT06392204 — CAD/CAM Angle Fracture Reduction/Plate Guide and Customized 3D Grid Plate Versus Champy’s Technique

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment24
Study TypeINTERVENTIONAL
ConditionsMandibular Fractures
Interventions;

This proposed study aims at creating a computer designed patient specific device and titanium plates, that are 3D manufactured in accordance to a preoperative computer aided virtual surgical procedure, aiming to obtain proper alignment of fractured segments of the lower jaw and restore proper teeth positioning therefore overcoming the possible complications of the conventional methods.

Recruit…

NCT07573033 — Effectiveness of Postoperative Topical and Oral Antibiotics on Impacted Mandibular 3rd Molar Surgery.

StatusCompleted
PhasePhase 4
SponsorLiaquat College of Medicine and Dentistry
Enrollment90
Study TypeINTERVENTIONAL
ConditionsImpacted Tooth; Postoperative Complications in Maxillofacial Surgery; Surgical Wound Infection; Facial Pain
Interventions;

This randomized controlled trial evaluates the effectiveness of postoperative topical antibiotics compared with oral antibiotics in patients undergoing surgical extraction of impacted mandibular third molars. The study aims to compare postoperative outcomes including infection, dry socket, pain, swelling, recovery time, patient satisfaction, and adverse effects associated with antibiotic use. A…

NCT07385924 — Evaluation of the Accuracy of 3d Printed Reduction Guide in Treatment of Mandibular Fractures Using Two Different Methods of Virtual Planning

StatusCompleted
PhasePhase 4
SponsorAlexandria University
Enrollment24
Study TypeINTERVENTIONAL
ConditionsMandibular Fracture; Virtual Plan of Mandibular Fracture
Interventions;

This study will evaluate the accuracy of the use of 3-D printed reduction guide in treatment of mandibular fractures using two different methods of virtual planning.

NCT06512532 — Fireworks Eye Injuries During Festivals in Upper Egypt

StatusCompleted
PhaseN/A
SponsorAssiut University
Enrollment59
Study TypeOBSERVATIONAL
ConditionsOcular Injury; Blast Injuries
Interventions

The aim of this study is to explore and report the epidemiology and outcome of fireworks ocular injuries in Upper Egypt.

Primary outcome : type and severity of injury of fireworks eye trauma during festives.

Secondary outcome: demography, complications, and final visual outcome of fireworks eye injury.

NCT07499726 — Precision of Patient Specific 3D Printed Occlusal Stent, Surgical Guide, and Patient Specific Titanium Plates in Management of Mandibular Fracture (Case Series)

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment6
Study TypeOBSERVATIONAL
ConditionsMandibular Fractures
Interventions

This study evaluates the accuracy of preoperative fully computerized occlusal stents, surgical guide, and patient-specific titanium plates in guided mandibular fracture reduction and fixation. The research question is: Does the use of patient-specific three-dimensional (3D) printed occlusal stents, surgical guides, and titanium plates accurately reduce mandibular fractures regarding guided frac…

NCT06588075 — A Full Digital VS Conventional Protocol in Management of Zygomatico-Maxillary Complex Fracture

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment28
Study TypeINTERVENTIONAL
ConditionsZygomatic Fractures
Interventions;

this study aims To evaluate The Accuracy of Zygomatico- Maxillary Complex (ZMC) Fracture reduction and fixation Using customized Patient-Specific implant and patient-specific predictive holes surgical guide Versus Conventional Technique of reduction and fixation.

NCT07245758 — Facial iD Customized Mandible Reconstruction Plates

StatusCompleted
PhaseN/A
SponsorStryker Craniomaxillofacial
Enrollment50
Study TypeOBSERVATIONAL
ConditionsMandibular Fractures; Mandible Fracture; Mandible; Deformity; MANDIBLE; Orthognathic Surgical Procedures
Interventions

A retrospective post market follow up to confirm the safety and performance of Stryker’s Customized Plates for Mandibular Reconstruction. The study is performed to confirm the product’s performance and safety by systematically collecting clinical data on its use.

NCT07221916 — Stryker’s Surgeon iD Mandible Reconstruction Plates: A Retrospective Post Market Follow Up

StatusCompleted
PhaseN/A
SponsorStryker Craniomaxillofacial
Enrollment70
Study TypeOBSERVATIONAL
ConditionsMandible Fracture; Mandibular Reconstruction
Interventions

A retrospective post market follow up to confirm safety and performance of Stryker’s Surgeon iD Plates (SMRP) medical device. The study is performed to confirm the product’s performance and safety by systematically collecting clinical data on its use.

NCT07551154 — Virtual Surgical Planning of Mandibular Reconstruction Using Custom Made Plate and Split Rib Bundle Bone Graf

StatusCompleted
PhaseN/A
SponsorAlexandria University
Enrollment30
Study TypeINTERVENTIONAL
ConditionsMandibular Injuries
Interventions

In mandibular reconstruction, computer-assisted procedures, including virtual surgical planning (VSP) and Custom-made implants, have become an integral part of routine clinical practice. Especially complex cases with extensive defects after ablative tumor surgery benefit from a computer-assisted approach. Various CAD/ CAM-manufactured tools such as surgical guides (guides for osteotomy, resecti…

NCT06774287 — Evaluation of the Karman Line Memory Strategy Training

StatusCompleted
PhaseN/A
SponsorKlimmendaal Revalidatiespecialisten
Enrollment6
Study TypeINTERVENTIONAL
ConditionsAcquired Brain Injury (Including Stroke)
Interventions;

Rationale: Acquired brain injury (ABI) often results in memory deficits that can have a big impact on social and vocational functioning of patients. Rehabilitation treatment of memory dysfunction consists of optimizing memory performance by using effective compensation strategies. Several effective memory-strategy training programs have been developed. However, these often contain labor-intensi…

NCT07590401 — Modified 3d Rectangular Grid Plate for Fixation of Anterior and Body Mandibular Fractures

StatusCompleted
PhaseN/A
SponsorAlexandria University
Enrollment22
Study TypeINTERVENTIONAL
ConditionsMandibular Fracture
Interventions;

Background: Fractures of anterior mandible (symphysis and parasymphysis) make up about 9% to 57%, of mandibular fractures, and body fractures make up about 21%; posing challenges for stabilization due to anatomical constraints. Traditional 3D plates have limitations in this area, leading to the development of Modified 3D Rectangular Grid plates. Studies have shown that these plates offer superi…

NCT07245719 — Stryker Universal Midface and Upper-Face Fixation System: A Retrospective Post Market Follow Up

StatusCompleted
PhaseN/A
SponsorStryker Craniomaxillofacial
Enrollment150
Study TypeOBSERVATIONAL
ConditionsZygomatic Fractures; Orbital Fractures; Maxilla Fractures; Facial Fractures
Interventions

A retrospective post-market clinical follow-up to confirm the performance and safety of the Upper-Face and Mid-Face modules of the Stryker Universal CMF System in a clinical setting. The study is performed to confirm the product’s performance and safety by systematically collecting clinical data on its use.

NCT07441538 — Optimizing the Timing for Facial Surgical Dressing Removal

StatusCompleted
PhaseN/A
SponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
Enrollment144
Study TypeINTERVENTIONAL
ConditionsNevus; Seborrheic Keratosis (SK); Cyst; Lipoma; Scar
Interventions

What is this study about? You are being invited to participate in a clinical research study because you are scheduled to undergo a facial skin surgery for your health condition. Your surgeon will perform your operation independently, and your standard surgical procedure and follow-up visits will not be changed in any way by this study.

The purpose of this research is to understand which postop…

NCT07384299 — Impact of Skin Type on Wonud Healing and Scarring Following Facial Skin Surgery

StatusCompleted
PhaseN/A
SponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
Enrollment173
Study TypeOBSERVATIONAL
ConditionsNevus; Seborrheic Keratosis (SK); Cyst; Lipoma; Scar

The goal of this observational study is to learn how an individual’s skin type influences the wound healing process and scar formation in Chinese patients undergoing facial dermatologic surgery. The main questions it aims to answer are:

How does skin type affect the quality of wound healing after facial surgery?

How does skin type affect the formation of hypertrophic scars after facial surger…

NCT07624708 — Three-Arm Quasi-Experimental Study of App-Assisted Acceptance and Commitment Therapy for Post-Traumatic Stress Symptoms

StatusCompleted
PhaseN/A
SponsorUniversity of Central Punjab
Enrollment30
Study TypeINTERVENTIONAL
ConditionsPosttraumatic Stress Disorder
Interventions

The goal of this clinical trial is to compare the efficacy of three Acceptance and Commitment Therapy (ACT) delivery modalities in treating Post-Traumatic Stress Disorder (PTSD) in adult patients (ages 20-40) with mild to moderate PTSD severity in Pakistan.

The main questions it aims to answer are:

  1. Do participants show significant reductions in psychological inflexibility, emotional dysreg…

NCT07153120 — Erich Arch Bars, IMF Screws and Hybrid Arch Bars in the Management of Mandibular Fractures

StatusCompleted
PhaseN/A
SponsorMansoura University
Enrollment24
Study TypeINTERVENTIONAL
ConditionsMandibular Fractures
Interventions; ;

Treatment options of mandibular fractures can be accomplished with either closed treatment or open reduction internal fixation (ORIF). Maxillomandibular fixation (MMF) refers to any method used to secure the maxilla and mandible in proper dental occlusion. MMF is a standard component of mandibular fracture management essential for closed treatment and commonly used du ring ORIF. Its three main …

NCT07543042 — Evaluation of the Sedative Effect of Contextualized Music Listening on Patient Pain and Anxiety in a Dental Care Setting

StatusCompleted
PhaseN/A
SponsorRawane El Dimachki
Enrollment30
Study TypeINTERVENTIONAL
ConditionsDental Pain; Dental Anxiety
Interventions; ;

The goal of this clinical study is to determine whether listening to culturally and personally contextualized music can reduce pain and anxiety in adults undergoing dental procedures. It will also examine how this intervention affects physiological responses related to stress.

The main questions it aims to answer are:

  • Does listening to a preselected, patient-chosen musical sequence reduce p…

Other (Terminated)

NCT05694247 — Study to Evaluate the Clinical Safety and Performance of the CorNeat KPro for Treatment of Corneal Blindness

StatusTerminated
PhaseN/A
SponsorCorNeat Vision Ltd.
Enrollment15
Study TypeINTERVENTIONAL
ConditionsCorneal Disease; Corneal Opacity; Corneal Injuries
Interventions

A Single Arm, Pivotal, Open Label, Multicenter Clinical Investigation to Evaluate the Clinical Safety and Performance of the CorNeat Keratoprosthesis, for Treatment of Corneal Blindness