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Lactate Blood Increase clinical trials

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NCT ID: NCT03831685 Recruiting - Sepsis Clinical Trials

Blood Lactate Level for Pre-hospital Orientation of Septic Shock

LAPHSUS
Start date: March 1, 2018
Phase:
Study type: Observational

In the pre-hospital setting, the severity assessment of septic shock is essential to decide the optimal initial in-hospital level of care. As clinical signs can be faulted, there is a need for an additional element in order to enhance the severity assessment and to decide in-hospital admission in the intensive care unit (ICU) or in the emergency department (ED). Point of care medical device yielding blood lactate levels since the pre-hospital setting may give an easy and valuable element for the severity assessment and the decision-making. The aim of this study is to provide clinical evidence that the pre-hospital blood lactate level predicts the 30-day mortality of patients with septic shock.

NCT ID: NCT03115970 Not yet recruiting - Trauma, Multiple Clinical Trials

Feasibility of Lactate Level Evaluation in Prehospital Care in Trauma

Start date: May 1, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Capillary or venous lactate level evaluation in prehospital care could be simple and beneficial tool for optimising prehospital care in patients with severe trauma.

NCT ID: NCT03062683 Recruiting - Syncope Clinical Trials

Serum Lactate in Convulsive Syncopes Compared to Non-convulsive Syncopes

Start date: January 1, 2017
Phase: N/A
Study type: Observational

The investigators compared the serum lactate, serum prolactin and serum creatine kinase concentrations following convulsive and non-convulsive syncopes. The aim of the study was to investigate their importance as diagnostic markers in transient loss of consciousness.