Clinical Trials Logo

Larynx Disease clinical trials

View clinical trials related to Larynx Disease.

Filter by:

NCT ID: NCT04734483 Recruiting - Larynx Disease Clinical Trials

The Effectiveness of Reconstructive Microsurgery on the Clinical and Functional State of Laryngeal Stenosis

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

To improve diagnostic methods for patients with laryngeal stenosis for the optimal determination of the technique of surgical treatment.

NCT ID: NCT03843580 Completed - Anesthesia Clinical Trials

Transnasal Humidified Rapid-Insufflation Ventilatory Exchange (THRIVE) Could Decrease the Incidence of Oxygen Desaturation During Suspension Laryngoscopy: a Randomized Controlled Trial (Optilaryngo)

optilaryngo
Start date: April 23, 2019
Phase: N/A
Study type: Interventional

Suspension laryngoscopy is realised during apnea. In effect, surgeons are in the mouth of the patient and we can't have access at the aiways. So investigators like to use a Transnasal Humidified Rapid-Insufflation Ventilatory Exchange (THRIVE) to increase time of apnea and decrease the impact of oxygen desaturation.

NCT ID: NCT03269396 Enrolling by invitation - Larynx Clinical Trials

Laryngeal Allograft Transplantation

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

The purpose of this proposed study is to obtain safety and efficacy data on human laryngeal allograft transplantation in an effort to safely use these procedures as a viable reconstructive option for patients with severe laryngeal or laryngotracheal incompetence.

NCT ID: NCT01360580 Completed - Larynx Disease Clinical Trials

Swallowing Disorders After Prolonged Mechanical Ventilation

Deglutube
Start date: January 2011
Phase: N/A
Study type: Observational

Epidemiology study for evaluation of incidence of swallowing disorders (SD) after prolonged invasive ventilation (more than seven days), using a clinical statement. All consecutive patients are screened, and clinical evaluation is performed during 48h after patient's extubation. If a SD exist, a new evaluation is realized 48h after. Three groups will be created (1.no SD, 2.transitory SD and 3.persistent SD (eg persistent after 48h)). Data complementary are notified at day 28 (pneumonia? nutritional status?)

NCT ID: NCT00567658 Withdrawn - Larynx Disease Clinical Trials

Effect of Acid Suppression With Esomeprazole on Vocal Cord Granulomas

Start date: February 2008
Phase: Phase 3
Study type: Interventional

The purpose of this research study is to measure the effects of the drug, esomeprazole 40 mg (Nexium) or placebo (inactive drug) on vocal cord granulomas.

NCT ID: NCT00444145 Completed - Clinical trials for Gastroesophageal Reflux

Do Laryngeal Tissue Changes in Patients Suspected of Having Laryngopharyngeal Reflux Predict Response to Treatment?

biopsy II
Start date: March 2007
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine if tissue changes are predictor of clinical response to therapy. The hypothesis is that the patients who have laryngeal signs and symptoms related to acid reflux, will have ultrastructural changes on a laryngeal biopsy which are predictors of response to therapy.

NCT ID: NCT00388453 Completed - GERD Clinical Trials

Efficacy of Dx-pH Probe in Diagnosing Extra-esophageal Reflux Disease

ADHERE
Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to establish the clinical application of a new device that records pH changes in the hypopharynx. The investigators also aim to compare the consistency of distal esophageal pH with hypopharyngeal pH using both the "short" and the "long" catheters in patients.

NCT ID: NCT00373997 Completed - Clinical trials for Gastroesophageal Reflux

Esophageal and Laryngeal Tissue Changes in Patients Suspected of Having Laryngopharyngeal Reflux

biopsy I
Start date: September 2006
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine whether patients with suspected Laryngopharyngeal reflux have inflammation and ultrastructural injury on their laryngeal biopsies.

NCT ID: NCT00372918 Completed - Larynx Disease Clinical Trials

Interpretation of Transnasal Esophagoscopy Findings

TNE
Start date: September 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the prevalence of esophageal pathology in patients with voice disorders. In addition, , the intra- and interdisciplinary variability regarding the identification of esophageal pathology will be analyzed in this study.

NCT ID: NCT00335283 Completed - Larynx Disease Clinical Trials

Efficacy of Lansoprazole in Chronic Post Nasal Drip

PND
Start date: August 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether aggressive acid suppression with Lansoprazole is effective in the treatment of post nasal drip, and also assess the predictors of response based on clinical and physiologic parameters.