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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Unity Health Toronto |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Exacerbation 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Indiana University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Skull 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Helwan University |
| Enrollment | 23 |
| Study Type | INTERVENTIONAL |
| Conditions | Nasal 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Alexandria University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Preterm; 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.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ricard Mellado Artigas |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Guy’s and St Thomas’ NHS Foundation Trust |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Surgery; 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Maria Sklodowska-Curie National Research Institute of Oncology |
| Enrollment | 225 |
| Study Type | INTERVENTIONAL |
| Conditions | CerebroSpinal 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Angers |
| Enrollment | 230 |
| Study Type | INTERVENTIONAL |
| Conditions | Endocrine; 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Kafrelsheikh University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | CSF 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
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | University of California, Berkeley |
| Enrollment | 65 |
| Study Type | INTERVENTIONAL |
| Conditions | Dry 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Riphah International University |
| Enrollment | 42 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical 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
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Zhejiang University |
| Enrollment | 220 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Istanbul University - Cerrahpasa |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Medical 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ohio State University |
| Enrollment | 500 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute 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
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | University of Tennessee |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Facial 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Nebraska |
| Enrollment | 10 |
| Study Type | OBSERVATIONAL |
| Conditions | Cardiac 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 258 |
| Study Type | INTERVENTIONAL |
| Conditions | Radiation-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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Nasal 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?”
| Status | Completed |
| Phase | N/A |
| Sponsor | Nemours Children’s Clinic |
| Enrollment | 73 |
| Study Type | INTERVENTIONAL |
| Conditions | Epistaxis |
| 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Yonsei University |
| Enrollment | 56 |
| Study Type | INTERVENTIONAL |
| Conditions | Foreign 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Dokuz Eylul University |
| Enrollment | 145 |
| Study Type | INTERVENTIONAL |
| Conditions | Respiratory 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.
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 144 |
| Study Type | INTERVENTIONAL |
| Conditions | Chest 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Wang Jianhui |
| Enrollment | 322 |
| Study Type | OBSERVATIONAL |
| Conditions | Bronchopulmonary 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Universidad de Granada |
| Enrollment | 20987 |
| Study Type | INTERVENTIONAL |
| Conditions | Acne; 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).
| Status | Completed |
| Phase | N/A |
| Sponsor | Rambam Health Care Campus |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Ventilator 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 38 |
| Study Type | INTERVENTIONAL |
| Conditions | Infant, 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Ioannina |
| Enrollment | 192 |
| Study Type | INTERVENTIONAL |
| Conditions | Trauma-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
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Ondine Biomedical Inc. |
| Enrollment | 322 |
| Study Type | INTERVENTIONAL |
| Conditions | Surgical 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Istanbul University - Cerrahpasa |
| Enrollment | 56 |
| Study Type | INTERVENTIONAL |
| Conditions | Pressure 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Bezmialem Vakif University |
| Enrollment | 114 |
| Study Type | INTERVENTIONAL |
| Conditions | Supraglottic 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Muhammad |
| Enrollment | 104 |
| Study Type | INTERVENTIONAL |
| Conditions | Traumatic 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Christiana Care Health Services |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Bronchopulmonary 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
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Lakehead University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Diphenhydramine 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
| Status | Completed |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Ondine Biomedical Inc. |
| Enrollment | 28 |
| Study Type | INTERVENTIONAL |
| Conditions | Healthcare 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Alexandria University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Ventilator 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Muğla Sıtkı Koçman University |
| Enrollment | 146 |
| Study Type | INTERVENTIONAL |
| Conditions | Respiratory 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Bach Mai Hospital |
| Enrollment | 285 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute 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
| Status | Terminated |
| Phase | Early Phase 1 |
| Sponsor | Thunder Bay Regional Health Research Institute |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Lung 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
| Status | Unknown |
| Phase | N/A |
| Sponsor | Daping Hospital and the Research Institute of Surgery of the Third Military Medical University |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Bronchopulmonary 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
| Status | Terminated |
| Phase | N/A |
| Sponsor | Vapotherm, Inc. |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Infant, 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)
| Status | Unknown |
| Phase | N/A |
| Sponsor | Hospital Universitari Vall d’Hebron Research Institute |
| Enrollment | 26 |
| Study Type | INTERVENTIONAL |
| Conditions | High-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
| Status | Unknown |
| Phase | N/A |
| Sponsor | Ain Shams University |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Traumatic 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
| Status | Unknown |
| Phase | N/A |
| Sponsor | Ordu University |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Nasal 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
| Status | Unknown |
| Phase | N/A |
| Sponsor | Assiut University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Nasal 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
| Status | Unknown |
| Phase | Phase 4 |
| Sponsor | Lakehead University |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Heat 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
| Status | Unknown |
| Phase | N/A |
| Sponsor | Medical University of Gdansk |
| Enrollment | 80 |
| Study Type | OBSERVATIONAL |
| Conditions | Nasal 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
| Status | Unknown |
| Phase | N/A |
| Sponsor | Rigshospitalet, Denmark |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Pre-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
| Status | Unknown |
| Phase | Phase 3 |
| Sponsor | Taichung Veterans General Hospital |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Traumatic 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
| Status | Unknown |
| Phase | N/A |
| Sponsor | Aswan University |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Maxillofacial 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
| Status | Withdrawn |
| Phase | Phase 4 |
| Sponsor | Vanderbilt University Medical Center |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Edema; 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…