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Thoracic Epidural Anesthesia clinical trials

View clinical trials related to Thoracic Epidural Anesthesia.

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NCT ID: NCT06068166 Completed - Clinical trials for Heart Failure With Reduced Ejection Fraction

Thoracic Epidural Anesthesia Reduces Mortality and Rehospitalization for Patients With Heart Failure With Reduced Ejection Fraction

Start date: July 1, 2013
Phase: N/A
Study type: Interventional

Despite significant scientific breakthrough in management, patients with heart failure with reduced ejection fraction (HFrEF) remain high morbidity and mortality, with a 5-year survival rate of 25% after hospitalization for HFrEF. The autonomic nervous system (ANS), particularly the sympathetic nervous system (SNS), plays a critical compensatory role in maintaining cardiovascular homeostasis in the failing heart. This is critical given the huge unmet need for novel treatment strategies for HFrEF. Thoracic epidural anesthesia (TEA), the infusion of anesthetic agents (eg, lidocaine or ropivacaine) into the epidural space, is used to achieve sympathetic block at the T1 to T4 levels in thoracic and abdominal surgical procedures. Since 1995, Professor Liu Fengqi has pioneered the use of TEA to treat end-stage HFrEF and achieved surprising results. TEA could reduce the enlarged heart cavity, halt and reverse cardiac remodeling, and improve cardiac systolic and diastolic function. Currently, thousands of HFrEF patients have received TEA procedure. However, it is unclear whether TEA could positively impact the clinical outcomes of patients with HFrEF.

NCT ID: NCT03826186 Completed - Clinical trials for Thoracic Epidural Anesthesia

CompuFlo Thoracic Epidural Study

Start date: March 26, 2019
Phase: N/A
Study type: Interventional

Traditionally, loss-of-resistance (LOR) to air or saline with a special ground-glass syringe is the technique used to identify epidural space, but failure rates up to 30% have been reported using this technique for thoracic epidural placement. This failure rate has sparked the search for newer techniques to improve the success rate for placement.The CompuFlo epidural system is a device that provides anesthesiologists and other healthcare providers the ability to quantitatively determine and document the pressure at the needle tip in real time. The device's proprietary dynamic pressure sensing technology (DPS) allows it to provide objective visual and audible in-tissue pressure feedback that allows anesthesiologists to identify the epidural space. The purpose this research study is to compare the success rate of the two different approaches (traditional method v/s CompuFlo assisted) to thoracic epidural placement.

NCT ID: NCT02135016 Completed - Clinical trials for Gastrointestinal Surgery

The Effect of Thoracic Epidural Anesthesia With Different Block Level on Propofol Induction

Start date: April 2014
Phase: Phase 4
Study type: Interventional

It is a prospective, randomized, placebo-controlled study to investigate the effect of TEA with different block level on propofol concentration during general anesthesia induction.

NCT ID: NCT02000973 Completed - General Anesthesia Clinical Trials

Effects of Epidural Local Anesthetics on Propofol Induction

Start date: November 2013
Phase: Phase 4
Study type: Interventional

The investigators designed a prospective, randomized, placebo-controlled study to determine whether thoracic epidural anesthesia(TEA) with different local anesthetics has different influences on the propofol dose during induction.