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Anesthesia, Endotracheal clinical trials

View clinical trials related to Anesthesia, Endotracheal.

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NCT ID: NCT06420947 Completed - Clinical trials for Anesthesia, Endotracheal

Application of Electrically Driven Atomized Surface Anesthesia

Start date: January 29, 2021
Phase: N/A
Study type: Interventional

This is a parallel and randomized-controlled clinical study aimed to identify the optimized size of atomized particles of 2% lidocaine that can provide the best topical anesthesia during ATI. To determine the effect of nebulization with different sizes of atomized particles of 2% lidocaine on cough, reaction, and comfort during ATI in patients with predicted difficult airway.

NCT ID: NCT06382831 Not yet recruiting - Clinical trials for Anesthesia and Analgesia

Opioid Free Versus Opioid Balanced Anesthesia in Ophthalmic Surgery

Start date: June 1, 2024
Phase: Phase 2/Phase 3
Study type: Interventional

Anesthesia without the use of opioid (Opioid free anesthesia) is an alternative to conventional opioid balanced anesthesia, with less post operative nausea and vomiting, and comparable analgesia. This study aim to compare the effect of opioid free versus opioid balanced anesthesia in ophthalmology surgery

NCT ID: NCT06380244 Recruiting - Anesthesia, General Clinical Trials

Opioid-free Anesthesia as an Alternative to General Anesthesia in Abdominal Surgery

Start date: March 10, 2024
Phase: N/A
Study type: Interventional

Due to the increasing number of reports of cancer progression in people undergoing surgery under general anesthesia using opioids, OFA is believed to have a favorable long-term prognostic effect, especially in cancer patients. The opioid-free protocol is also used in postoperative analgesia. It is estimated that up to 75% of surgical patients experience chronic postoperative pain, which has a particularly negative impact on the quality of life. The investigators would like to compare pain during the first 48 postoperative hours of patients undergoing abdominal surgery who would be anesthetized with opioids and without opioids (patients would be randomly assigned to a group) (1, 2, 6, 12, 24 and 48 h after operations). A secondary objective will be to measure total oxycodone consumption in the postoperative period in both groups. Other secondary objectives: assessment of postoperative nausea and vomiting (PONV).

NCT ID: NCT06231342 Recruiting - Clinical trials for Anesthesia, Endotracheal

Endotracheal Tube (ETT) 180: Stylet-loaded Endotracheal Tube Rotation Before Insertion

Start date: May 31, 2023
Phase: N/A
Study type: Interventional

The main objective of the proposed study is to clarify whether rotating a stylet-loaded endotracheal tube (ETT) 180 degrees prior to intubation will decrease the incidence of postoperative throat soreness, when compared to standard technique used in Standard of Care.

NCT ID: NCT05296668 Completed - Neonate Clinical Trials

Cuffed Versus Uncuffed Tracheal Tubes in Neonates Undergoing Elective Surgery

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

This thesis aims to assess the safety and efficacy of usage of cuffed ETT in neonate undergoing elective surgeries.

NCT ID: NCT03582787 Completed - Clinical trials for Anesthesia, Endotracheal

A Comparison of McGrath MAC Videolaryngoscopy and Macintosh Laryngoscopy for Orotracheal Intubation in Children With Torticollis

Start date: May 31, 2018
Phase: N/A
Study type: Interventional

The primary purpose of this study is to investigate the effects of McGrath MAC videolaryngoscopy on the intubation time for orotracheal intubation in children with torticollis. The secondary purpose of this study is to investigate the effects of McGrath MAC videolaryngoscopy on Cormack and Lehane Grade for orotracheal intubation in children with torticollis.

NCT ID: NCT03524586 Completed - Airway Management Clinical Trials

Comparison of the Cuff Pressure of a Taper-guard Cuffed Tube Between Ipsilateral and Contralateral Rotation of Head

Start date: January 2, 2018
Phase: N/A
Study type: Interventional

This study evaluates the endotracheal tube cuff pressure of a taper-guard cuffed tube during tympanoplasty with ipsilateral rotation of head, compared to the contralateral rotation of head. The investigators will performed the ipsilateral rotation of head against the fixed tube in half of participants or the contralateral rotation of head in the other half.

NCT ID: NCT03396432 Completed - Surgery Clinical Trials

The Videolaryngoscopy in Small Infants

VISI
Start date: June 4, 2018
Phase: N/A
Study type: Interventional

Complications related to infant (≤ 1 year) airway management are under-appreciated because of few rigorous and targeted studies. Investigators have recently shown that multiple tracheal intubation (TI) attempts are a key risk factor for intubation-related complications in small children. Tracheal Intubation using Video laryngoscopy (VL) has become popular in anesthesiology practice because of several advantages over conventional direct laryngoscopy (DL). Studies show that VL improves the view of the airway compared to DL, requires fewer intubation attempts, but may take more time to intubate the trachea. This study compares first attempt success of VL to DL in infants presenting for elective surgery.

NCT ID: NCT03155555 Completed - Clinical trials for Mechanical Ventilation

Comparison of Carotid Peak Systolic Velocity Variation With Aortic Peak Systolic Velocity Variation in Pediatric Non-Cardiac Surgery

Start date: December 2016
Phase:
Study type: Observational

The purpose of this study is to evaluate whether carotid Doppler peak systolic velocity can be an easy to measure possible surrogate for echocardiographic measurement of aortic peak systolic velocity variation which is an index of fluid responsiveness in mechanically ventilated children intra-operatively.

NCT ID: NCT03094754 Completed - Clinical trials for Anesthesia, Endotracheal

Excision Size and Location on the Postoperative Pain After Nevi Excision in Children

Start date: March 13, 2017
Phase:
Study type: Observational

The primary purpose of this study is to investigate the effects of excised surface area/body surface area ratio and location of excision on the postoperative pain after nevi excision in children. The primary purpose of this study is to investigate the effects of excised surface area/body surface area ratio and location of excision on the emergence excitation after nevi excision in children.