Clinical Trials for Nose Injuries and Disorders

Currently registered clinical trials for Nose Injuries and Disorders from ClinicalTrials.gov. 11 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 Nose Injuries and Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 11
  • Active, not recruiting: 0
  • Completed: 22
  • Other: 17

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

Recruiting Trials

NCT03033251 — High Flow Nasal Cannula Versus Non-Invasive Ventilation in Exacerbations of Chronic Obstructive Pulmonary Disease

StatusRecruiting
PhaseN/A
SponsorUnity Health Toronto
Enrollment30
Study TypeINTERVENTIONAL
ConditionsExacerbation Copd; Acute Respiratory Distress; Acute Hypercapnic Respiratory Failure
Interventions; ;

Chronic obstructive lung disease is a disabling disease that affects people usually after several years of smoke tobacco exposure and affects millions of patients worldwide. The disease is marked by multiples episode of worsening, termed exacerbations necessitating frequent hospitalizations. During these exacerbations, patients present breathless, and in the most severe cases, are admitted to a…

NCT05898074 — Role of Novel RADA16 Hydrogel in Endoscopic Skull Base Surgery

StatusRecruiting
PhaseN/A
SponsorIndiana University
Enrollment30
Study TypeINTERVENTIONAL
ConditionsSkull Base Neoplasms; Cerebrospinal Fluid Leakage; Nasal; Hypertrophy, Mucous Membrane (Septum)
Interventions;

The purpose of this study is to specifically evaluate the effectiveness of PuraGel, a RADA16 polypeptide hydrogel, in expediting post-operative healing and re-mucosalization of the nasoseptal flap harvest site during endoscopic skull base surgery and the impact on patient and sinonasal morbidity.

NCT06439927 — New Method to Close Nasal Septal Perforation

StatusRecruiting
PhaseN/A
SponsorHelwan University
Enrollment23
Study TypeINTERVENTIONAL
ConditionsNasal Perforated Septum
Interventions

The goal of this clinical trial is to investigate if a 3-dimensional fabricated nasal mesh works to close nasal septal perforations. Under general anesthesia, during nasal septal perforation repair surgery, the investigator will place the mesh between the elevated mucoperichondrial flaps opposite the site of the perforation and confirm its original position at both sides under nasal endoscope. …

NCT06550219 — Evaluation of Nasal Non Invasive Ventilation in Management of Neonates With Respiratory Distress Using Lung Ultrasound

StatusRecruiting
PhaseN/A
SponsorAlexandria University
Enrollment30
Study TypeINTERVENTIONAL
ConditionsPreterm; Ventilator Lung; Newborn
Interventions; ;

This study aims to evaluate the effect of non-invasive ventilation (nIPPV)

, (nCPAP), and nasal high flow cannula (NHFC) as a primary mode of ventilation in preterm neonates <37 gestational week with moderate to severe RD using LUS as regard: I. Primary outcomes: Duration of non-Invasive ventilation. II. Secondary outcomes: Evaluation LUS over the 1 st 7 days of life or weaning from ventilati…

NCT06694311 — Physiologic Effects of Continuous Positive Airway Pressure and High Flow Nasal Oxygenation in Patients with Acute Respiratory Distress Syndrome.

StatusRecruiting
PhaseN/A
SponsorRicard Mellado Artigas
Enrollment120
Study TypeINTERVENTIONAL
ConditionsAcute Respiratory Distress Syndrome (ARDS); Acute Respiratory Failure with Hypoxia
Interventions;

The acute respiratory distress syndrome (ARDS) consists on a lack of breath due to fluid overload in the lungs that is not produced by a heart desease. Some people with this condition may need to be intubated and connected to invasive mechanical ventilation, but less severe cases may need supplementary oxygen that can be delivered with non-invasive devices, such as CPAP (continuous positive air…

NCT06731881 — Assessing the Efficacy of Photodynamic Therapy for Preventing Surgical Site Infections

StatusRecruiting
PhaseN/A
SponsorGuy’s and St Thomas’ NHS Foundation Trust
Enrollment80
Study TypeINTERVENTIONAL
ConditionsSurgery; Nasal Disease; Light; Therapy, Complications
Interventions; ;

This is a randomised, unblinded interventional device proof of concept pilot trial in which patients undergoing nasal surgery will be selected for either photodisinfection therapy (PDT) with the Steriwave™ ND System, or control with nares swabbed with ‘photosensitizer formulation’ preoperatively.

This trial will primarily assess the safety and efficacy of nasal photodisinfection treatment in d…

NCT07216157 — NoSeal Trial: Comparing Sealants Versus No Sealant for Preventing CSF Leak After Endonasal Skull Base Surgery

StatusRecruiting
PhaseN/A
SponsorMaria Sklodowska-Curie National Research Institute of Oncology
Enrollment225
Study TypeINTERVENTIONAL
ConditionsCerebroSpinal Fluid (CSF) Leak
Interventions; ;

Postoperative cerebrospinal fluid (CSF) leak is a significant complication of endoscopic endonasal approaches (EEA) to the skull base. The use of tissue sealants such as fibrin glue (Tisseel) or synthetic agents (PEI/PEG) is widespread in surgical practice, however, recent high-quality evidence challenges their clinical benefit and cost-effectiveness. This study aims to investigate whether the …

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…

NCT07368348 — Evaluation of Internal Nasal Splint-Supported Free Graft Versus Nasoseptal Flap for Endoscopic Skull Base Repair in Cerebrospinal Fluid Leaks

StatusRecruiting
PhaseN/A
SponsorKafrelsheikh University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsCSF Leak
Interventions;

The study aims to compare the feasibility and effectiveness of using an internal nasal splint- supported free graft versus a nasoseptal flap alone for endoscopic repair of bilateral CSF leaks.

Research question:

Does the use of an internal nasal splint to support a free graft during endoscopic repair of bilateral CSF leaks improve outcomes compared to the use of a nasoseptal flap alone?

NCT07606625 — Ocular Surface Health and Tear Film Stability With a Nasal Spray Dry Eye Treatment

StatusRecruiting
PhasePhase 4
SponsorUniversity of California, Berkeley
Enrollment65
Study TypeINTERVENTIONAL
ConditionsDry Eye; Meibomian Gland Dysfunction
Interventions

The purpose of this study is to examine the impact of nasal spray treatment on Meibomian gland function and ocular surface health in symptomatic dry eye patients with mild to moderate Meibomian gland dysfunction (MGD).

NCT07645027 — Low Volume Nose Resistance Breathing Exercise With Incentive Spirometer in Patient With Cervical Spinal Cord Injuries

StatusRecruiting
PhaseN/A
SponsorRiphah International University
Enrollment42
Study TypeINTERVENTIONAL
ConditionsCervical Spinal Cord Injury; Cervical Cord Injuries Spinal
Interventions;

This randomized clinical trial aims to evaluate the effectiveness of combining Low Volume Nose Resistance Breathing Exercises (LVNRBE) with Incentive Spirometry (IS) on respiratory outcomes in patients with cervical spinal cord injury (SCI). Respiratory complications are a major concern in cervical SCI due to impaired respiratory muscle function, leading to reduced lung volumes, dyspnea, ineffe…

Not Yet Recruiting

NCT06945926 — The Effect of Oxytocin Nasal Spray on Preventing Postoperative Delirium in Elderly Patients Undergoing Orthopedic Surgery

StatusNot yet recruiting
PhasePhase 2
SponsorZhejiang University
Enrollment220
Study TypeINTERVENTIONAL
ConditionsCervical Spinal Stenosis; Thoracic Spinal Stenosis; Lumbar Spinal Stenosis; Rotator Cuff Injury; Femoral Head Necrosis
Interventions

Postoperative delirium is a delirium that occurs within 7 days after surgery or before hospital discharge. It has been shown that combined POD can increase the incidence of postoperative pulmonary infections, deep vein thrombosis and decubitus ulcers, and increase the incidence of disability and mortality. The incidence of postoperative delirium in geriatric orthopedics is high.

Investigators …

NCT07521410 — Non-Invasive Ventilation Interfaces and Nasal Pressure Injury in Preterm Infants

StatusNot yet recruiting
PhaseN/A
SponsorIstanbul University - Cerrahpasa
Enrollment75
Study TypeINTERVENTIONAL
ConditionsMedical Device-Related Pressure Injury; Prematurity
Interventions; ;

The goal of this randomized controlled clinical trial is to learn whether different non-invasive ventilation interfaces can prevent medical device-related nasal pressure injury in preterm infants receiving respiratory support in a neonatal intensive care unit.

The main questions it aims to answer are:

  • Do different non-invasive ventilation interfaces affect how often nasal pressure injury de…

NCT07558265 — WIN Ratio Analysis to Determine a Strategy of Non- Invasive SUpport for Respiratory Failure in the EmeRgency Department

StatusNot yet recruiting
PhaseN/A
SponsorOhio State University
Enrollment500
Study TypeINTERVENTIONAL
ConditionsAcute Hypoxic Respiratory Failure; Acute Respiratory Distress Syndrome (ARDS)
Interventions;

The purpose of this clinical trial is to determine the best initial non-invasive respiratory support (NIRS) strategy for adults who present to the emergency department with acute hypoxemic respiratory failure, a condition in which blood oxygen levels are dangerously low and require urgent treatment. This study compares two commonly used non-invasive respiratory support strategies to evaluate th…

Enrolling by Invitation

NCT06850857 — Multi-Institutional IMPACT Validation

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of Tennessee
Enrollment500
Study TypeOBSERVATIONAL
ConditionsFacial Injuries; Mandible Fracture; Le Fort; Zygomaticomaxillary Complex Fracture; Nasal Fracture
Interventions; ;

The goal of this observational study is to validate a novel patient-reported outcome measure (PROM) for patients suffering maxillofacial trauma: The Integrated Modular Patient-Reported Outcome Assessment for Craniomaxillofacial Trauma (IMPACT). The primary question is:

Are the IMPACT modules valid and reliable measures to study quality-of-life (QOL) in patients with maxillofacial trauma?

Pati…

Completed Trials

NCT00577798 — Cardiac Magnetic Resonance Imaging in Patients With Non-Hodgkin Lymphoma or Hodgkin Lymphoma Receiving Doxorubicin

StatusCompleted
PhaseN/A
SponsorUniversity of Nebraska
Enrollment10
Study TypeOBSERVATIONAL
ConditionsCardiac Toxicity; Chemotherapeutic Agent Toxicity; Lymphoma
Interventions

RATIONALE: Diagnostic procedures, such as cardiac magnetic resonance imaging, may help doctors detect early changes in the heart caused by chemotherapy.

PURPOSE: This clinical trial is studying how well cardiac magnetic resonance imaging works in patients with newly diagnosed non-Hodgkin lymphoma or Hodgkin lymphoma receiving doxorubicin.

NCT02589938 — Trial of Acupuncture for Radiation-Induced Xerostomia in Head and Neck Cancer

StatusCompleted
PhaseN/A
SponsorWake Forest University Health Sciences
Enrollment258
Study TypeINTERVENTIONAL
ConditionsRadiation-Induced Xerostomia; Head and Neck Cancer; Radiation Toxicity; Oral Complications of Chemotherapy and Head/Neck Radiation
Interventions; ;

This study is being done to find out what effects, good and/or bad, acupuncture has on participants and their xerostomia caused by radiation therapy for the treatment of the cancer.

NCT03159624 — Nasal Septal Flap for Donor Site Reconstruction

StatusCompleted
PhaseN/A
SponsorUniversity of Alabama at Birmingham
Enrollment47
Study TypeINTERVENTIONAL
ConditionsNasal Septum Perforation
Interventions;

The purpose of this study is to demonstrate the utility of porcine small intestinal submucosa (SIS) as a graft material that may aid in the natural healing process of freshly exposed bone and cartilage in the nasal cavity.

NCT02517294 — , “Mucosal Injury During Nasotracheal Intubation for Dental Procedures in Children-does the Tube Design Matter?”

StatusCompleted
PhaseN/A
SponsorNemours Children’s Clinic
Enrollment73
Study TypeINTERVENTIONAL
ConditionsEpistaxis
Interventions;

Comparison is made between standard nasotracheal tubes and a specially designed nasotracheal tube during nasotracheal intubation in children undergoing general anesthesia for dental surgery.

NCT03892408 — High-flow Nasal Oxygen During Rigid Bronchoscopy Under General Anesthesia: a Randomized Controlled Trial

StatusCompleted
PhaseN/A
SponsorYonsei University
Enrollment56
Study TypeINTERVENTIONAL
ConditionsForeign Bodies; Tumor; Stenosis Trachea; Bronchus Tumour
Interventions

The aim of this study is to evaluate the effect of high-flow nasal cannula oxygen administration on apnea in patients undergoing general anesthesia with rigid bronchoscopy compared with standard anesthesia methods.

NCT05031650 — Open Lung Strategy During Non-Invasive Respiratory Support of Very Preterm Infants in the Delivery Room

StatusCompleted
PhaseN/A
SponsorDokuz Eylul University
Enrollment145
Study TypeINTERVENTIONAL
ConditionsRespiratory Distress Syndrome in Premature Infant; Non-invasive Ventilation; Lung Injury
Interventions;

The opening and aeration of the lung is critical for a successful transition from fetal to neonatal life. Early nasal CPAP in the delivery room in spontaneously breathing premature babies with a gestational age of 30 weeks or less is a standard treatment approach since it reduces the need for invasive mechanical ventilation and surfactant therapy. In respiratory distress syndrome (RDS) manageme…

NCT03943914 — Early Non-invasive Ventilation and High-flow Nasal Oxygen Therapy for Preventing Delayed Respiratory Failure in Hypoxemic Blunt Chest Trauma Patients.

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Bordeaux
Enrollment144
Study TypeINTERVENTIONAL
ConditionsChest Injuries; Respiratory Failure
Interventions;

In blunt chest trauma patients without immediate life-threatening conditions, delayed respiratory failure and need for mechanical ventilation may still occur in 12 to 40% of patients, depending on the severity of the trauma, the preexisting conditions and the intensity of initial management.

In this context, non-invasive ventilation (NIV) is recommended in hypoxemic chest trauma patients, defi…

NCT04184648 — Comparison of Classification Standards of Bronchopulmonary Dysplasia (BPD) in Premature Infants

StatusCompleted
PhaseN/A
SponsorWang Jianhui
Enrollment322
Study TypeOBSERVATIONAL
ConditionsBronchopulmonary Dysplasia
Interventions

Bronchopulmonary dysplasia of premature infants is a common respiratory disease in premature infants. Long-term complications such as recurrent respiratory infection and abnormal lung function may occur in the survivors, and may increase the risk of dysplasia of the nervous system. In the past 30 years, although the monitoring and treatment technology of premature infants has been significantly…

NCT05247333 — Implementation of a Minor Ailment Service in Community Pharmacy Practice

StatusCompleted
PhaseN/A
SponsorUniversidad de Granada
Enrollment20987
Study TypeINTERVENTIONAL
ConditionsAcne; Bites; Burns; Cold; Cold Sore Mouth
Interventions

Self-care and self-medication are commonly the treatments of choice for the management of minor ailments. Minor ailments can be treated through community pharmacy using a Minor Ailment Service (MAS). The INDICA+PRO Impact Study, evaluated the clinical, economic and humanistic impact of a MAS, concluding that community pharmacies could greatly benefit the health system. Thus, the following objec…

NCT04836689 — Influence of Respiratory Rate Settings on CO2 Levels During Nasal Intermittent Positive Pressure Ventilation (NIPPV).

StatusCompleted
PhaseN/A
SponsorRambam Health Care Campus
Enrollment50
Study TypeINTERVENTIONAL
ConditionsVentilator Lung; Newborn
Interventions

Infants will be monitored by TcCO2 during three consecutive time periods of one hour each on a high and low rate of NIPPV, when in a stable condition. NIPPV rate will start high/low, changed to low/high and switched back to starting rate.

NCT04792099 — CPAP Or Nasal Cannula Oxygen for Preterm Infants: A Randomized Controlled Trial

StatusCompleted
PhaseN/A
SponsorUniversity of Alabama at Birmingham
Enrollment38
Study TypeINTERVENTIONAL
ConditionsInfant, Newborn, Disease; Hypoxia; Respiratory Distress Syndrome; Bronchopulmonary Dysplasia
Interventions;

The purpose of this study is to determine if in preterm infants < 34 weeks’ gestation at birth receiving respiratory support with continuous positive airway pressure (CPAP) or nasal cannula (NC), CPAP compared with NC will decrease the number of episodes with oxygen saturations less than 85% of ≥10 seconds in a 24-hour randomized controlled trial. This will be a randomized controlled trial wit…

NCT05563129 — Teaching First Aid and Trauma Management to School Students

StatusCompleted
PhaseN/A
SponsorUniversity of Ioannina
Enrollment192
Study TypeINTERVENTIONAL
ConditionsTrauma-related Wound; Head Injury; Choking; Nose Bleed; Child, Only
Interventions

This proposal aims to describe research that will utilize first aid in primary education students and will attempt to identify the frequency with which the training should be repeated and the type of trainer who will carry out the training program.

NCT05090657 — Nasal Photodisinfection in All Patients Presenting for Surgery for a Wide Range of Surgical Procedures

StatusCompleted
PhasePhase 2
SponsorOndine Biomedical Inc.
Enrollment322
Study TypeINTERVENTIONAL
ConditionsSurgical Site Infections; Nosocomial Infection; Healthcare Associated Infections
Interventions

This is a Phase 2 single-center, open-label, single-arm, study of a microbiological endpoint using antimicrobial photodynamic therapy (aPDT) for nasal disinfection in all patients (universal) presenting for surgery at an acute care hospital for a wide range of surgical procedures.

NCT06325215 — The Effect of Hydrocolloid to Prevent Nasal Injuries in Preterm Infants

StatusCompleted
PhaseN/A
SponsorIstanbul University - Cerrahpasa
Enrollment56
Study TypeINTERVENTIONAL
ConditionsPressure Injury
Interventions

The aim of this study is to evaluate the effect of using hydrocolloid tapes in preventing pressure injuries on the nose and columella regions caused by non-invasive mechanical ventilation (NIMV) in preterm infants.

NCT05360810 — Wei Nasal Jet Tube vs Gastro Laryngeal Tube in Endoscopic Retrograde Cholangiopancreatography

StatusCompleted
PhaseN/A
SponsorBezmialem Vakif University
Enrollment114
Study TypeINTERVENTIONAL
ConditionsSupraglottic Airway Efficiency; Airway Complication of Anesthesia; Airway Aspiration; Complication of Anesthesia; Esophagus Injury
Interventions;

The most common adverse event in endoscopic procedures is hypoxia. Different airway devices have been investigated in the literature to prevent hypoxia. This study aimed to compare the efficacy and procedural performance of two different airway (GLT and WNJ) devices in ERCP procedures.

NCT06304012 — Effect of Oral Enteral Nutrition on Severe Traumatic Brain Injury

StatusCompleted
PhaseN/A
SponsorMuhammad
Enrollment104
Study TypeINTERVENTIONAL
ConditionsTraumatic Brain Injury
Interventions; ;

This was a multicenter randomized controlled study of 98 severe Traumatic Brain Injury patients with tracheostomy. Patients enrolled were divided randomly into the observation group with Intermittent Oro-esophageal Tube Feeding (n=50) or the control group with Nasogastric tube feeding (n=48) for enteral nutrition support, respectively. Nutritional status, complications, decannulation of tracheo…

NCT05547139 — Impact of Extended CPAP on Bronchopulmonary Dysplasia

StatusCompleted
PhaseN/A
SponsorChristiana Care Health Services
Enrollment20
Study TypeINTERVENTIONAL
ConditionsBronchopulmonary Dysplasia; Prematurity
Interventions

The purpose of this pilot study is to compare if keeping infants on CPAP (continuous positive airway pressure) support for an extended period of time until they are 32 weeks corrected gestational age or 1250 grams (approximately 2 pounds and 12 ounces) will decrease their degree of lung disease as compared to weaning their respiratory support to HFNC (high flow nasal cannula).

NCT05586477 — Diphenhydramine and Sweating

StatusCompleted
PhasePhase 4
SponsorLakehead University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsDiphenhydramine Causing Adverse Effects in Therapeutic Use; Hyperthermia; Allergic Rhinitis; Sweating
Interventions;

In 2012, it was estimated that nearly 1 in 4 Canadians suffer from allergic rhinitis. To add, 78% of individuals working in predisposing environments are predicted to develop occupational rhinitis. Currently, the most popular treatment for rhinitis is antihistamine medication such as diphenhydramine, a first-generation antihistamine sold commercially as Benadryl®. Due it its anticholinergic eff…

NCT05797818 — Red Light Photobiomodulation and Topical Disinfectants

StatusCompleted
PhasePhase 1 / Phase 2
SponsorOndine Biomedical Inc.
Enrollment28
Study TypeINTERVENTIONAL
ConditionsHealthcare Associated Infection; Nosocomial Infection; Surgical Site Infection
Interventions; ;

The goal of this clinical trial is to evaluate the potential effects of photobiomodulation when used with topical disinfectants in the anterior nares of healthy adults.

Over a three week period, participants will have their anterior nares swabbed with methylene blue, chlorhexidine gluconate, or a combination of the two followed by 4 minutes of non-thermal red light treatment. The fourth week o…

NCT05706428 — Cardiorespiratory Effects of Nasal High Frequency Ventilation in Neonates

StatusCompleted
PhaseN/A
SponsorAlexandria University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsVentilator Lung; Newborn; Hemodynamic Instability; Echocardiography
Interventions;

The aim of the present work is to study the cardio-respiratory effects of non-invasive ventilation (nasal high-frequency ventilation and nasal CPAP) as an initial therapy of respiratory distress in moderate and late preterm infants as regard:

I. Primary outcomes:

  • Duration of the non- invasive respiratory support.
  • Need of invasive ventilation in the first 72 hours.
  • Short-term complicatio…

NCT06549283 — Nasal Intermittent Positive Pressure Ventilation During Neonatal Intubation

StatusCompleted
PhaseN/A
SponsorMuğla Sıtkı Koçman University
Enrollment146
Study TypeINTERVENTIONAL
ConditionsRespiratory Distress Syndrome; Intubation; Difficult or Failed; Newborn Morbidity; Desaturation of Blood; Ventilator Lung; Newborn
Interventions

The study aims to determine whether the use of nasal intermittent positive pressure ventilation (NIPPV) during neonatal endotracheal intubation increases the rate of successful intubation without physiological instability during all intubation attempts.

The present study was designed as a prospective, multicenter, randomized, controlled study conducted with neonates undergoing endotracheal int…

NCT07664085 — High-Flow Nasal Cannula After Extubation in Acute Brain Injury

StatusCompleted
PhaseN/A
SponsorBach Mai Hospital
Enrollment285
Study TypeOBSERVATIONAL
ConditionsAcute Brain Injury; Post-neurosurgical Status; Extubation Failure; Postoperative Respiratory Complications; Reintubation

Patients with acute brain injury after neurosurgery are at increased risk of extubation failure after removal of the endotracheal tube. High-flow nasal cannula (HFNC) may provide better post-extubation respiratory support than conventional oxygen therapy (COT), but evidence in post-neurosurgical patients remains limited.

This prospective observational study evaluated adult post-neurosurgical p…

Other (Terminated)

NCT02748798 — Developing Optimal Parameters for Hyperpolarized Noble Gas and Inert Fluorinated Gas MRI of Lung Disorders

StatusTerminated
PhaseEarly Phase 1
SponsorThunder Bay Regional Health Research Institute
Enrollment10
Study TypeINTERVENTIONAL
ConditionsLung Transplant; Lung Resection; Lung Cancer; Asthma; Cystic Fibrosis
Interventions; ;

The goal of this research is to optimize the MRI system to obtain ideal lung images using Hyperpolarized (HP) Noble and Inert Fluorinated Gases as contrast agents. Lung coils tuned to the frequencies of these gases will be used. This study will take place at TBRHSC in the Cardiorespiratory Department and in the Research MRI facility.

Other (Unknown)

NCT04905732 — Nasal High-frequency Oscillatory Ventilation (NHFOV) for Ventilated Newborn Infants With BPD

StatusUnknown
PhaseN/A
SponsorDaping Hospital and the Research Institute of Surgery of the Third Military Medical University
Enrollment200
Study TypeINTERVENTIONAL
ConditionsBronchopulmonary Dysplasia; Nasal High-frequency Oscillatory Ventilation; Nasal Continuous Positive Airway Pressure; Neonate
Interventions;

Invasive ventilation(IV) remains one key cornerstone to reduce neonatal mortality for preterm infants with respiratory distress syndrome(RDS) and/or acute respiratory distress syndrome(ARDS). However, it is also related to increased risks of ventilator-associated lung injury and escalation of pulmonary inflammation, and which finally result in bronchopulmonary dysplasia (BPD). Early weaning fro…

NCT05030012 — Maintaining Optimal HVNI Delivery Using Automatic Titration of Oxygen in Preterm Infants

StatusTerminated
PhaseN/A
SponsorVapotherm, Inc.
Enrollment15
Study TypeINTERVENTIONAL
ConditionsInfant, Premature; Neonatal Respiratory Distress; Oxygen Saturation; Bronchopulmonary Dysplasia
Interventions;

Oxygen treatment is common in management of preterm babies requiring intensive care. Delivery of too much or too little oxygen increase the risk of damage to eyes and lungs, and contributes to death and disability. Oxygen control in preterm infants requires frequent adjustments in the amount of oxygen delivered to the baby. This is generally performed manually by a clinician attending the baby,…

NCT05401474 — Individualization Flow in Patients Treated With High Flow Nasal Therapy (iFLOW)

StatusUnknown
PhaseN/A
SponsorHospital Universitari Vall d’Hebron Research Institute
Enrollment26
Study TypeINTERVENTIONAL
ConditionsHigh-Flow Nasal Cannula; Oxygen Therapy; Acute Respiratory Failure; Respiratory Failure; Lung Injury
Interventions; ;

In patients with acute hypoxemic respiratory failure (AHRF), High Flow Nasal Therapy (HFNT) improves oxygenation, tolerance, and decreases work of breathing as compared to standard oxygen therapy by facemask.

The hypothesis is that this flow challenge (ROX index variation from 30 to 60L/min) could be used as a test for assessing changes in lung aeration, analyzed by the variation in end expira…

NCT05509088 — Impact of the Early Use of High Flow Nasal Cannula in Patients With Post-traumatic Lung Contusion, a Randomized Clinical Trial

StatusUnknown
PhaseN/A
SponsorAin Shams University
Enrollment120
Study TypeINTERVENTIONAL
ConditionsTraumatic Lung Injury
Interventions

We hypothesize that early and continuous administration of oxygen via high flow nasal cannula in patients with lung contusion and non-severe acute lung injury might reduce the incidence of intubation and hold the deterioration of pulmonary functions.

NCT05844345 — The Effect of Hydrocolloid Tape and Facial Massage in Premature Infants During Noninvasive Mechanical Ventilation

StatusUnknown
PhaseN/A
SponsorOrdu University
Enrollment120
Study TypeINTERVENTIONAL
ConditionsNasal Injury
Interventions;

The aim of this study is to assess the effect of nasal injury prevention interventions (NIPI) (hydrocolloid tape and facial massage) on nasal septum injury, stress and comfort of premature neonates (28-35 weeks gestation) receiving non-invasive mechanical ventilation (NIMV) support.

NCT06070311 — Wound Healing After Endoscopic Sinus Surgery

StatusUnknown
PhaseN/A
SponsorAssiut University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsNasal Polyps; Chronic Sinusitis
Interventions

This study aims to determine the effect of Thymoquinone (0.5%) and olive oil ointment on Wound healing after Endoscopic sinus surgery.

NCT06217367 — Over-the-Counter Antihistamines & Heat Stress

StatusUnknown
PhasePhase 4
SponsorLakehead University
Enrollment16
Study TypeINTERVENTIONAL
ConditionsHeat Illness; Allergic Rhinitis; Heat Injury; Sudomotor Sympathetic Dysfunction
Interventions; ;

Allergic rhinitis (AR) currently affects ~25% of Canadians, and due to factors of climate change, this number is expected to increase over the coming decade. AR symptoms can significantly impact individuals’ quality of life by compromising sleep, productivity, and social interactions. To alleviate AR symptoms, North Americans tend to rely on H1 antihistamine medications available over-the-coun…

NCT06163209 — Ultrasonography in the Diagnosis of Nasal Fractures

StatusUnknown
PhaseN/A
SponsorMedical University of Gdansk
Enrollment80
Study TypeOBSERVATIONAL
ConditionsNasal Bone Fracture; Nasal Injury; Facial Injuries; Nasal Deformity, Acquired; Nose; Wound
Interventions;

The purpose of this cross-sectional prospective observational study is to determine the efficacy of high-resolution ultrasonography in identifying and characterizing nasal bone fractures in adult patients with recent facial trauma. The primary questions it aims to answer are:

  • Can high-resolution ultrasonography effectively detect nasal bone fractures?
  • Is high-resolution ultrasonography cap…

NCT05629910 — NeO2Matic-Pilot Trial

StatusUnknown
PhaseN/A
SponsorRigshospitalet, Denmark
Enrollment30
Study TypeINTERVENTIONAL
ConditionsPre-Term; Respiratory Distress Syndrome, Newborn; Retinopathy of Prematurity; Bronchopulmonary Dysplasia
Interventions

The main goal of this trial is to test if:

automated adjustment of supplemental oxygen to preterm infants in noninvasive respiratory support based on feedback from a measurement of blood-oxygen saturation

results in more stable blood-oxygenation compared to routine nurse controlled adjustment of oxygen

NCT06290219 — The Effect of Platelet-rich Plasma Nasal Injection in the Treatment of Traumatic Olfactory Dysfunction

StatusUnknown
PhasePhase 3
SponsorTaichung Veterans General Hospital
Enrollment80
Study TypeINTERVENTIONAL
ConditionsTraumatic Olfactory Nerve Injury With Anosmia (Diagnosis); Effect of Drug
Interventions; ;

The purpose of this study is to explore the efficacy of injecting high-concentration platelet plasma combined with hyaluronic acid into the nasal olfactory mucosa in the treatment of traumatic anosmia.

NCT06386757 — Comparison Between Nasal and Oropharyngeal Bleeding in Video Laryngoscopy and Direct Laryngoscopy for Nasal Intubation

StatusUnknown
PhaseN/A
SponsorAswan University
Enrollment64
Study TypeINTERVENTIONAL
ConditionsMaxillofacial Injuries; Nasal Bleeding; Intubation Complication
Interventions;

The objective of this study is to compare the effectiveness and safety of video laryngoscopy versus direct laryngoscopy for nasal intubation in patients with maxillofacial fractures regarding less bleeding to oral and nasal structures, quicker intubation times, increased success rates for first intubation attempts, fewer uses of the Magill forceps and the less need for cervical spine extension

Other (Withdrawn)

NCT06483204 — Steroids for Rhinoplasty: Pain, Nausea, Edema and Ecchymosis

StatusWithdrawn
PhasePhase 4
SponsorVanderbilt University Medical Center
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsEdema; Bruising; Nasal Obstruction; Postoperative Pain; Postoperative Nausea
Interventions

This study will be a prospective randomized study to evaluate the effect of medrol dosepaks (oral corticosteroids) on postoperative outcomes among patients undergoing rhinoplasty by Facial Plastic Surgeons at Vanderbilt. Outcomes will include postoperative pain, nausea, and patient experience, with secondary outcomes of swelling and bruising.

Methylprednisolone is an oral corticosteroid that h…