Return of Aspiration-Free Swallow After Laryngotracheal Anesthesia
NCT04575870 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2024-04-24
Summary
Patients undergo laryngotracheal anesthesia (LTA) for a variety of in-office laryngology procedures. Prior to resolution of laryngeal sensory anesthesia, oral intake may predispose patients to aspiration. The purpose of this study is to objectively characterize a time period for return of aspiration-free swallow after LTA.
Conditions
- Swallowing, Air
Interventions
- OTHER
-
waiting period
amount of time between clinical procedure and modified functional endoscopic exam of swallowing
Sponsors & Collaborators
-
University of Alabama at Birmingham
lead OTHER
Principal Investigators
-
Blake Simpson, MD · University of Alabama at Birmingham
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-11-18
- Primary Completion
- 2023-01-31
- Completion
- 2023-01-31
Countries
- United States
Study Locations
More Related Trials
-
Effects of an Swallowing and Oral Care Program in Patients Following Prolonged Endotracheal Intubation
NCT02334774 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of Laryngeal Mask Airways in Sinonasal Surgery
NCT02311153 ·Status: COMPLETED ·Phase: NA
-
Voice Analysis as a Predictor for Difficult Intubations
NCT04105738 ·Status: TERMINATED
-
The Effect of Lidocaine on Smooth Emergence With Double Lumen Tube
NCT04455711 ·Status: UNKNOWN ·Phase: NA
-
Effect of Paratracheal Esophagus Pressure on the Insertion of Laryngeal Mask Airway
NCT04106635 ·Status: COMPLETED ·Phase: NA
-
Evaluating Potential Risk of Choking by Laryngeal Ultrasound in Patients With Acute Stroke
NCT04874454 ·Status: RECRUITING ·Phase: NA
-
Superior Laryngeal Nerve Block For Awake Endotracheal Intubation Study
NCT01848548 ·Status: TERMINATED
-
Tongue Root Retractor For Fibroscopic Intubation
NCT04343014 ·Status: COMPLETED ·Phase: NA
-
Laryngeal Mask Airway Facilitates a Safe and Smooth Emergence From Anesthesia in Patients Undergoing Craniotomy
NCT05253404 ·Status: COMPLETED ·Phase: NA
-
Forearm-Supported Head Extension to Decrease Dental Contact
NCT05495880 ·Status: UNKNOWN ·Phase: NA
-
Post-extubation Assessment of Laryngeal Symptoms and Severity
NCT03726086 ·Status: COMPLETED
-
The Routine Use of Nasopharyngeal Airway in the Setting of Monitored Anesthesia Care During Gastrointestinal Endoscopy
NCT04123821 ·Status: COMPLETED ·Phase: NA
-
Voice Therapy With a Semi-occluded Vocal Tract
NCT06137131 ·Status: COMPLETED ·Phase: NA
-
Accuracy of Upper Lip Bite Test and Measurement of Skin-to-epiglottis Distance in Predicting Difficult Laryngoscopy: a Prospective Observational Study
NCT05881694 ·Status: UNKNOWN
-
The Use of PEDI_ EAT 10 Score Versus Nurse Performed Screening in the Assessment of Post Extubation Dysphagia
NCT05828537 ·Status: UNKNOWN
-
Assessment of Post-operative Sore Throat After Scheduled General Anesthesia
NCT04115865 ·Status: WITHDRAWN
-
Relationship Between Optimal Laryngeal Mask Airway Cuff Volume and Physical Examination of Head and Neck
NCT02502422 ·Status: COMPLETED ·Phase: NA
-
Laryngeal Mask Airway (LMA) Insertion With Sevoflurane and Remifentanil
NCT01456299 ·Status: COMPLETED ·Phase: NA
-
Effects of Topical Anesthesia With Pressure Nebulized 2% Lidocaine During Awake Intubation
NCT01185535 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Valuation of Swallowing in Patient Sedated for Gastroenteric Endoscopic Procedure
NCT01789424 ·Status: COMPLETED
-
The Appropriate Remifentanil Dose for Optimal Insertion of Laryngeal Mask Airway in Adult Patients During Induction of General Anesthesia Using Remimazolam.
NCT06289829 ·Status: RECRUITING ·Phase: NA
-
Comparison of Ambu Auragain and I-Gel Supraglottic Airways in Adult Patients at an Ambulatory Surgery Center
NCT04286581 ·Status: COMPLETED ·Phase: NA
-
Paratracheal Esophagus Pressure on the Intubation With Pentax Airway Scope
NCT04135651 ·Status: COMPLETED ·Phase: NA
-
The Impact of Suction- Assisted Laryngoscopy and Airway Decontamination on Intubation Times
NCT04082403 ·Status: UNKNOWN ·Phase: NA
-
No Post Intubation Laryngeal Symptoms
NCT05383417 ·Status: COMPLETED ·Phase: NA