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Laryngismus clinical trials

View clinical trials related to Laryngismus.

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NCT ID: NCT05339880 Recruiting - Arrythmia Clinical Trials

Relation Between Oculocardiac Reflex and Laryngospasm

Start date: January 4, 2021
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to evaluate whether there is a significant relation between various arrhythmias during the surgeon's stretching the eye muscles and laryngospasm and emergence agitation in strabismus surgeries

NCT ID: NCT04947397 Recruiting - Anesthesia Clinical Trials

Investigation of Pupillometry as Guide for Extubation Readiness in Anesthetized Children

Start date: June 20, 2022
Phase: N/A
Study type: Interventional

Investigation of pupillometry as guide for extubation readiness in anesthetized children.

NCT ID: NCT04159116 Completed - Hypoxemia Clinical Trials

Prevention and Treatment of Laryngospasm and Hypoxemia Based on Risk Factors in Adult Outpatients Undergoing EGD

Start date: November 4, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to identify patient and provider-chosen factors that put patients at risk for the development of hypoxemia (oxygen saturation < 90% for 5 seconds) during endoscopy and to use this knowledge to develop a treatment protocol for specific causes of hypoxemia in adult esophagogastroduodenoscopy outpatients.

NCT ID: NCT04113720 Completed - Levobupivacaine Clinical Trials

Levobupivacaine vs Levobupivacaine + Dexmedetomidine Infiltration for Post-tonsillectomy Analgesia and Laryngospasm in Pediatric Patients

Start date: November 15, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Tonsillectomy is one of the most common surgical performed procedures in children. Adenotonsillectomy surgery in pediatrics is commonly managed as an ambulatory surgery. This may be attributed to the use of the electro-dissection surgical technique that decreases the incidence of immediate postoperative hemorrhage. However, the use of the electro-cautery technique increases postoperative inflammation. Postoperative throat pain is a very important and significant problem because it can lead to decreased oral intake and dehydration with subsequent serious complications of dehydration.

NCT ID: NCT01456299 Completed - Laryngismus Clinical Trials

Laryngeal Mask Airway (LMA) Insertion With Sevoflurane and Remifentanil

Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study was to determine the most suitable effect-site concentration of remifentanil for the LMA insertion during inhaled induction with 8% sevoflurane in adults.

NCT ID: NCT01445847 Terminated - Laryngospasm Clinical Trials

The Effect of Intravenous Lidocaine on Post-extubation Laryngospasm

Start date: January 2012
Phase: N/A
Study type: Interventional

In the literature, we found no randomized clinical trials addressing the using of IV lidocaine as prophylaxis for postoperative laryngospasm among adults. The aim of this study was to assess the effects of IV lidocaine on the incidence of postoperative laryngospasm of adults patients.

NCT ID: NCT01288248 Active, not recruiting - Bradycardia Clinical Trials

Noninferiority Clinical Trial With Laryngeal Mask and Endotracheal Tube

Start date: January 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the use of laryngeal mask classic as method for securing the airway in the population of 2 years to 14 years is associated with risk of laryngospasm as compared with the use of endotracheal tube.

NCT ID: NCT00665418 Terminated - Laryngospasm Clinical Trials

Sevoflurane and Laryngeal Reflex Responses in Pediatric Patients

Start date: February 2008
Phase: Phase 4
Study type: Interventional

To describe laryngeal and respiratory reflex responses after controlled laryngeal stimulation in pediatric patients anesthetized with sevoflurane and to compare the evoked responses at two levels of anesthesia. To determine whether laryngeal and respiratory reflex responses after controlled laryngeal stimulation are completely suppressed in subjects when anesthetized with a MACEI95 (EI = endotracheal intubation) sevoflurane Hypothesis: The incidence of apnea with laryngospasm evoked by laryngeal stimulation will be reduced by 20% (from 25% to 5%) when the end-tidal concentration of sevoflurane is increased from 2.5% (MAC50) to 4.7% (MACEI95)