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Total Intravenous Anesthesia clinical trials

View clinical trials related to Total Intravenous Anesthesia.

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NCT ID: NCT06269328 Completed - Sleep Disorder Clinical Trials

Measuring Sleep Quality In Patients That Posterior Spinal Instrumentatıon Plannıng

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

Postoperative sleep disorders have serious problems with cognition, pain perception, sustained circadian rhythm, psychomotor function, metabolic function, catabolic responses, and continuity. The relationship between general anesthesia and sleep disturbances following surgery is still unclear. Since the risk of sleep disorders after surgery is high, it is important to determine the efficiency of the interval with automatic sleep disorders. By evaluating how major orthopedic surgery and general anesthesia applied to posterior spinal instrumentation divides sleep quality, risk management allows determining the factors involved in the peroperative period and thus facilitating surgical results and patient comfort.

NCT ID: NCT05046223 Completed - Lung Diseases Clinical Trials

Comparison of iGel and THRIVE on Bronchoscopic Interventions

Start date: August 20, 2021
Phase: N/A
Study type: Interventional

THRIVE and iGEL were applied for maintain oxygenation in bronchoscopic interventions which could not performed with an endotracheal tube. However, besides the risk of desaturation, the differences on difficulties to approach vocal cords, the responses to spay of local anesthetics including cough or spasm, the CO2 elimination, the hemodynamic changes, and the effects on postoperative recovery are rarely investigated.

NCT ID: NCT04394897 Completed - Propofol Clinical Trials

Total Intravenous Anesthesia With Remifentanil-propofol Admixture

Start date: March 12, 2013
Phase:
Study type: Observational

Background: Application of total intravenous anesthesia (TIVA) may be considered as unpractical when compared with inhalational anesthesia. Although it is mostly not recommended, mixing intravenous agents seems to be popular in clinical practice. The aim of the study was to investigate the possible clinical drawbacks of using remifentanil-propofol admixture (MIXTIVA) for TIVA.

NCT ID: NCT04048226 Completed - Clinical trials for Total Intravenous Anesthesia

Dexmedetomidine-Ketamine Infusion in Breast Surgeries

Start date: September 1, 2019
Phase: Phase 4
Study type: Interventional

- This is a prospective randomized double blind controlled study. - Female patients undergoing radical mastectomy will be included in this study where they will be randomly allocated into; - Control group in which patients will receive continuous infusion of normal saline. Dexmedetomidine-Ketamine group in which patients will receive continuous infusion of ketamine and dexmedetomidine. The intraoperative and postoperative opioid consumption will be measured. Also, the postoperative pain score and the incidence of chronic pain will be assessed.

NCT ID: NCT04036487 Completed - Quality of Recovery Clinical Trials

Effects of General Anesthesia on Quality of Recovery After Transaxillary Endoscopic Breast Augmentation

Start date: July 28, 2017
Phase: N/A
Study type: Interventional

Among aesthetic or cosmetic surgeries, breast augmentation was the most frequently performed and the endoscopic transaxillary approach has become the preferred incision for Asian women. As breast augmentation must be performed under general anesthesia accompanied by its effects and potential complications, types of general anesthesia may affect the quality of recovery. Currently, the two most common techniques of general anesthesia are inhalation anesthesia (IH) and total intravenous anesthesia (TIVA). The effects of these types of general anesthesia on the quality of recovery have been investigated for numerous surgical procedures. However, no prior studies have analyzed different types of anesthesia used for performing transaxillary endoscopic breast augmentation. This prospective, parallel, randomized controlled study will evaluate the effects of inhalation anesthesia vs. total intravenous anesthesia on the quality of recovery in patients undergoing transaxillary endoscopic breast augmentation.

NCT ID: NCT03727607 Completed - Obesity Clinical Trials

TIVA Versus Desfluran Anaesthesia in Patients Undergoing Bariatric Surgery

Start date: January 30, 2016
Phase: Phase 2
Study type: Interventional

Many factors during laparascopic surgery leads to PONV (postoperative nausea and vomiting), such as C02 insufflations causing peritoneal stretch and irritation and type of anaesthesia given during surgery. The two anesthetic techniques used in bariatric surgery are gas anesthesia (Remifentanil TCI and Desfluran) and Total Intra Venous Anesthesia (TIVA) with propofol. There are studies which have shown a reduction in postoperative nausea and vomiting following TIVA, and there are publications showing no statistically significant difference. The aim of this study was to investigate the best anaesthetic approach for obese subjects, evaluating awakening time, postoperative nausea and pain. Our hypothesis was based on the fact that Propofol is a lipid-soluble anesthetic and therefore might have a prolonged effect in obese patients, leading to a longer awakening time along with postoperative nausea and vomiting. This hypothesis is also described earlier by obese patients have more depots (bulk fat) and also more fat surface making anaesthetics storage more easier, and also that the anesthetic will return into the circulation when the administration is stopped [18].