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Adverse Anesthesia Outcome clinical trials

View clinical trials related to Adverse Anesthesia Outcome.

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NCT ID: NCT03015857 Completed - Clinical trials for Adverse Anesthesia Outcome

Phenylephrine and Noradrenaline for Post Spinal Anesthesia Hypotension

Start date: January 2017
Phase: Phase 2
Study type: Interventional

Hypotension following spinal anesthesia for cesarean section is a serious problem. In this study we investigated the effect of the vasopressors phenylephrine and noradrenaline on postspinal hypotension.

NCT ID: NCT02977559 Not yet recruiting - Clinical trials for Adverse Anesthesia Outcome

A Study Between the Laryngeal Tube Suction-Disposable and the Ambu AuraGain in Pediatric Patients

Start date: March 2017
Phase: N/A
Study type: Interventional

The study compared the Laryngeal Tube Suction Disposable (LTS-D) with the Disposable Laryngeal Mask Ambu® AuraGain™ (DLMA AG) during general anesthesia in pediatric patients. The investigators hypothesized that the LTS-D and the DLMA AG performed similarly during mechanical ventilation despite differences in their structural design.

NCT ID: NCT02884986 Completed - Clinical trials for Adverse Anesthesia Outcome

Analgesia in Inguinal Hernia Repair Using a Cyclooxygenase-2-specific Inhibitor

Start date: January 2015
Phase: N/A
Study type: Interventional

Acute pain is the result of activating nociceptive pathways in both the peripheral and central nervous system. The origin of most acute pain from surgical stimulation is the mechanical trauma of the local tissue and the subsequent acute inflammatory response. No studies have investigated the combined use of anti-inflammatory analgesics with spinal anaesthesia/analgesia for pre, intra and postoperative multimodal pain protection in patients undergoing day-case IHR. The aim of the investigators study is therefore to assess the efficacy of preoperative combined administration of etoricoxib and standard spinal anaesthesia in the reduction of postoperative pain following IHR.

NCT ID: NCT02884921 Completed - Clinical trials for Adverse Anesthesia Outcome

Preemptive Analgesia Using Intravenous Paracetamol

Start date: April 2015
Phase: N/A
Study type: Interventional

Dental treatment for children should be done in a calm atmosphere and without pain. Oral Propacetamol has been shown to be effective in a variety of postsurgical pain models. There are no studies on paracetamol preemptive analgesia effect on the pediatric population in the dental setting which compare analgesic effect when administered before Vs after the dental treatment. The investigators hypothesis is that preoperative intravenous paracetamol are helpful in the prevention of postoperative pain in children undergoing dental treatment.

NCT ID: NCT02884895 Not yet recruiting - Clinical trials for Adverse Anesthesia Outcome

A Comparison of Direct Laryngoscopy With Blind Intubation Via Intubating Laryngeal Tube Suction Disposable

Start date: April 2017
Phase: N/A
Study type: Interventional

Tracheal intubation is an important part of treatment for a trauma casualty. Tracheal intubation is usually achieved by a direct laryngoscope.It is an effective method but requires experience and skill demanding a long learning time.The use of the Laryngeal Tube Suction for fast control of the airway is known for many years. The Intubating Laryngeal Tube Suction is a new version of the Laryngeal Tube. The aim of this study is to examine the effectiveness of the the Intubating Laryngeal Tube Suction to achieve a definitive airway by unskilled practitioners in anesthetized patients with the head in neutral position (trauma model).

NCT ID: NCT02884869 Not yet recruiting - Clinical trials for Adverse Anesthesia Outcome

Comparison of Direct Laryngoscopy With Blind Intubation Via Intubating Laryngeal Mask Airway

Start date: August 2016
Phase: N/A
Study type: Interventional

Control the airways by endotracheal intubation is an important part of treatment for a trauma casualty. The use of the Laryngeal Mask Airway for fast control of the airway is known for many years. The aim of this study is to examine the effectiveness of the Intubating Laryngeal Mask Airway to achieve a definitive airway by unskilled practitioners. The hypothesis is that definitive airway obtaining with Intubating Laryngeal Mask Airway will be more success and faster compared to the standard way of direct laryngoscope.

NCT ID: NCT02884843 Not yet recruiting - Clinical trials for Adverse Anesthesia Outcome

The New Intubating Laryngeal Tube Suction-Disposable

Start date: August 2016
Phase: N/A
Study type: Interventional

The study compares the intubating Laryngeal Tube Suction (iLTS-D) with the Ambu®AuraGain™ in blind and fibreoptic endotracheal intubation. The current randomized study is designed to assess the success rate of blind and fibreoptic endotracheal intubation using i-LTS-D, in comparison with the Air-Q, i-gel® and Ambu®AuraGain™ in an airway simulator. The investigators hypothesize that the iLTS-D and the Supreme Laryngeal Mask Airway will similarly perform during spontaneous ventilation despite differences in their structural design.

NCT ID: NCT02883192 Recruiting - Clinical trials for Adverse Anesthesia Outcome

The Effect of Preventive Use of Ondansetron in the Cesarean Section Under Spinal Anesthesia

Start date: February 2016
Phase: N/A
Study type: Interventional

Cesarean section is a frequent procedure in the obstetric surgery. The most widely used anesthesia technique for cesarean delivery is the spinal anesthesia The incidence of spinal anesthesia induced hypotension and bradycardia is high as 60% in the obstetric population. The aim of the study is to investigate the effect of the preventive use of Ondansetron on the prevention of hypotension

NCT ID: NCT02866890 Not yet recruiting - Clinical trials for Adverse Anesthesia Outcome

The New Laryngeal Tube Suction-Disposable for Childrens

Start date: December 2016
Phase: N/A
Study type: Interventional

The Laryngeal Tube Suction Disposable( LTS-D) has recently undergone considerable structural changes in design. As these changes may influence the performance of the LTS-D relative to the old LTS-D version the investigator decided to check the new LTS-D in the pediatric version The investigator hypothesized that the LTS-D perform clinically well during general anesthesia with controlled ventilation.

NCT ID: NCT02859922 Completed - Clinical trials for Adverse Anesthesia Outcome

Comparison Between the Supreme Laryngeal Mask Airway and the Laryngeal Tube Suction During Spontaneous Ventilation

Start date: January 2009
Phase: N/A
Study type: Interventional

The study compared the Laryngeal Tube Suction (LTS-D) Disposable with the Supreme Laryngeal Mask Airway (SLMA) during spontaneous ventilation. The investigators hypothesized that the LTS-D and the SLMA perform similarly during spontaneous ventilation despite differences in their structural design.