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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: 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: 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.

NCT ID: NCT02856672 Completed - Clinical trials for Adverse Anesthesia Outcome

Trial Comparing the Laryngeal Tube Suction Disposable and the Supreme Laryngeal Mask Airway

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

The investigators study compared the Laryngeal Tube Suction-Disposable with the Supreme Laryngeal Mask Airway, hypothesizing that the two devices would provide adequate oropharyngeal seal pressure in different head and neck positions and perform similarly during pressure controlled ventilation in neutral position, despite differences in their structural design.

NCT ID: NCT02570269 Completed - Clinical trials for Adverse Anesthesia Outcome

Prospective Comparison of Oral Intubation Via - Ambu® Aura Gain™ vs Slotted Guedel Tubus

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

The study has to show that an intubation with the AuraGain Laryngeal mask could bring the same benefits in terms of intubation in clinical practice, as the slotted Guedel tubus.

NCT ID: NCT02252120 Completed - Clinical trials for Adverse Anesthesia Outcome

Laryngeal Mask Airway Supreme Versus Laryngeal Tube

Start date: January 2014
Phase: N/A
Study type: Interventional

The investigators test the hypothesis that oropharyngeal leak pressure and fiberoptic position differ between the size 2 LMA SupremeTM and the Laryngeal Tube LTS IITM in non-paralyzed anaesthetized pediatric patients

NCT ID: NCT01575236 Completed - Clinical trials for Adverse Anesthesia Outcome

A Randomized Non Crossover Study of the GuardianTM Versus SupremeTM Laryngeal Mask Airway

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

The investigators test the hypothesis that ease of insertion, oropharyngeal leak pressure, fiberoptic position and ease of gastric tube placement differ between the GuardianTM and the LMA SupremeTM in paralyzed, anesthetized patients.

NCT ID: NCT00468598 Completed - Clinical trials for Heart; Dysfunction Postoperative, Cardiac Surgery

The Prognostic Value of Troponin T for Long-term Outcome After Cardiac Surgery

Start date: January 2007
Phase: N/A
Study type: Observational

This survey has two aims. First, we would like to be informed about the health condition of our patients two years following heart surgery at University Hospital, Basel. Second, we are interested in determining whether a patient's long-term outcome can be predicted by the analysis of blood samples taken shortly after heart surgery.Troponin T, the blood parameter that we are interested in, is routinely assessed in the Intensive Care Unit. The purpose of this survey is to determine whether or not it is also possible to infer the long-term outcome from this blood parameter.