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Anesthesia clinical trials

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NCT ID: NCT03833947 Completed - Anesthesia Clinical Trials

Dexamethasone vs Bicarbonate to Intracuff Lignocaine 2% in General Anaesthesia

Start date: March 15, 2019
Phase: Phase 4
Study type: Interventional

This study is designed to evaluate and compare the effect on hemodynamics, extubation response and patients satisfaction score in patients with ETT cuff filled with either mixture of lignocaine with sodium bicarbonate or with a mixture of lignocaine with dexamethasone.

NCT ID: NCT03830086 Completed - Postoperative Pain Clinical Trials

Regional Anesthesia Versus General Anesthesia

Start date: February 7, 2019
Phase: N/A
Study type: Interventional

Patients undergoing laparoscopic gynecological surgery will receive regional anesthesia or general anesthesia with endotracheal intubation. The investigators aim to evaluate the feasibility and safety of regional anesthesia for laparoscopic gynecological procedures.

NCT ID: NCT03827083 Completed - Anesthesia Clinical Trials

Evaluation of Cognitive Functions by Cerebral Pulse Oximetry

Start date: January 9, 2019
Phase:
Study type: Observational

General and Spinal Anesthesia can be used in geriatric patients in orthopedic surgery. Post-op cognitive dysfunction can be seen in orthopedic surgeries in this group of patients. In this study, the investigators aimed to compare cognitive functions between spinal and general anesthesia using cerebral and systemic oxygenation, hemodynamic data and pre-op, post-op cognitive function tests.

NCT ID: NCT03818048 Completed - Anesthesia Clinical Trials

Inhaled Sevofluran vs Endovenous Propofol for Colonoscopy

Start date: January 1, 2016
Phase: N/A
Study type: Interventional

To compare the anesthetic efficacy of the inhalation versus intravenous technique for maintenance of sedation in patients undergoing endoscopy. A longitudinal, randomized clinical study of 32 patients of both sexes ASA I-III, aged 18-80 years undergoing diagnostic colonoscopy, which was randomly divided into 2 groups. In both, intravenous induction with propofol (2-2.5 mg / kg) was performed, Group A remained sedated with propofol infusion (1-2 mg / kg / min); Group B by inhalation with sevoflurane at a concentration of 2 vol% through a nasal cannula with an oxygen flow.

NCT ID: NCT03817879 Completed - Anesthesia Clinical Trials

Double-lumen Tubes (DLT) - Health Economic Study

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

The aim of this study is to make a health economic evaluation comparing novice physicians use of VivaSight double-lumen tube and a conventional double-lumen tube for single-lung ventilation during thoracic surgery at a teaching hospital. The hypothesis is, that both double-lumen tubes are equally cost-effective and the the incidence of fiberoptic bronchoscope use it the same for both tubes.

NCT ID: NCT03814330 Completed - Anesthesia Clinical Trials

A Comparison of Sedation/Analgesia & LMA on Anxiety Level and Patient Satisfaction in In-Vitro Fertilization

IVF
Start date: January 24, 2019
Phase: N/A
Study type: Interventional

In vitro fertilization (IVF) is a new expertise of our age. Anesthesia during the assisted reproduction technique is usually required during oocyte removal, which is one of the basic steps throughout the entire procedure. Until now, different anesthetic techniques such as conscious sedation, general anesthesia and regional anesthesia have been tried, no superiority has been proved against each other. The main point of anesthesia management in IVF is to minimize anesthesia exposure to avoid harmful effects on embryo division and fertilization. The aim of this prospective randomized clinical trial was to compare two different anesthesia applications (sedation & laryngeal mask airway) on anxiety and patient satisfaction in patients with IVF.

NCT ID: NCT03813303 Completed - Anesthesia Clinical Trials

Comparison of Post Anesthetic Recovery Time in Sedated Patients for Colonoscopy

CPART
Start date: March 20, 2018
Phase: Phase 4
Study type: Interventional

Colonoscopy is an important diagnostic and therapeutic tool in colon disorders. Different drugs and levels of sedation can be used in its accomplishment. There is no consensus on which is the ideal. The aim of this study was to compare the post anesthetic recovery time between patients deeply sedated with midazolam and propofol or fentanyl and propofol. 50 American Society of Anesthesiologist physical state (ASA) I and II candidates elective colonoscopy at Luxembourg Hospital were divided into two groups A) midazolam and propofol or B) fentanyl and propofol. Time of examination, post anesthetic recovery and discharge at home, intercurrence and propofol consumption were compared.

NCT ID: NCT03808753 Completed - Surgery Clinical Trials

Mini Fluid chAlleNge and End-expiratory Occlusion Test and to Assess flUid responsiVEness in opeRating Room

MANEUVER
Start date: February 27, 2019
Phase: N/A
Study type: Interventional

End-expiratory occlusion test (EEOT) has been previously successfully tested in surgical patients, consisting of the interruption of the mechanical ventilation for 30 seconds, and in the evaluation of the changes in the SV. The mini fluid challenge test (mFC) aims at testing the increase in SV after the rapid administration of a small aliquot of the predefined FC. Both these test have been previously evaluated in small-sized studies and never compared each other.

NCT ID: NCT03806374 Completed - Anesthesia Clinical Trials

Is it Possible to Replace Fentanyl in Anesthesia for Minor Procedures?

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

To compare between fentanyl group and ketamine lidocaine group for induction of anesthesia as regards hemodynamics and smooth intubation.

NCT ID: NCT03791424 Completed - Anesthesia Clinical Trials

Changes of Skin Resistance After Midazolam and After the End of Anaesthesia

Start date: October 1, 2014
Phase: Phase 4
Study type: Interventional

It has been described that sympathetic activity, measured as changes in electrical skin resistance (SR), may be used to assess the adequacy of general anaesthesia. Our prospective study investigated how far measurements of skin resistance can help determine level of sedation. The secondary aim was to investigate if changes in skin resistance can be used for assessing recovery from anaesthesia.