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Haemodynamic Instability clinical trials

View clinical trials related to Haemodynamic Instability.

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NCT ID: NCT06249113 Completed - Surgery Clinical Trials

Effectiveness of Continous Adjuvant Lidocaine on General Anaesthesia on Tumor Craniotomy Surgery

Start date: January 16, 2023
Phase: N/A
Study type: Interventional

This study aims to investigate the effect of adjuvant continuous lidocaine in General Anesthesia on Depth of Anesthesia (qCON), Pain Response (qNOX), and Blood Sugar Levels in Elective Primary Tumor Craniotomy Surgery

NCT ID: NCT05285800 Completed - Clinical trials for Haemodynamic Instability

To Determine the Effectiveness of Saddle Block vs Spinal Anesthesia in TURP

Start date: September 6, 2021
Phase: Phase 3
Study type: Interventional

To determine the effectiveness of saddle block vs spinal anesthesia in TURP.

NCT ID: NCT03395483 Completed - Colorectal Surgery Clinical Trials

Peripheral and Mesenteric Perfusion in Elective Surgical Patients

Start date: April 10, 2018
Phase:
Study type: Observational

An important goal of haemodynamic monitoring and resuscitation is early detection of insufficient tissue perfusion and oxygenation. The mesenteric haemodynamic response to circulatory shock is complex, and diagnosis of bowel ischaemia poses significant difficulty. Assuming blood flow is diverted from the peripheral tissue and the gastrointestinal tract to vital organs, during circulatory shock, an objective, simple and non-invasive method of detecting peripheral tissue perfusion impairment might detect this at an early stage. The peripheral perfusion index (PPI) reflects changes in peripheral perfusion and laser doppler flowmetry allows measurement of bowel tissue perfusion. The aim of this study is to explore the association between changes in peripheral and intestinal perfusion in patients undergoing elective colorectal surgery exposed to intraoperative haemodynamic challenges.

NCT ID: NCT03348488 Completed - Clinical trials for Haemodynamic Instability

Transcapillary Plasma Refill in Advanced Chronic Kidney Disease

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

Background: Haemodynamic instability during haemodialysis has long been linked to poor cardiovascular outcomes. It does not always reflect overall hydration but rather plasma volume depletion, with a delay in plasma refill from other body compartments, and vasodilatation, mediated by endothelial factors. Our understanding of these processes remains largely incomplete. Despite our ability to monitor relative blood volume during haemodialysis our knowledge concerning the factors affecting plasma refill remain incomplete. This may be due to variations observed between individuals. Understanding the pattern of fluid shifts variation between the different body compartment and the factors affecting these behaviours in different individuals or at different hydration states could be a vital component of our management of intradialytic haemodynamic instability but also overhydration. Aims and Objectives: The aim of this study is to describe plasma refill rate, during haemodialysis using a non-invasive, continuous, real-time data capture during ultrafiltration. The study will attempt to describe different refilling phenotypes in the study population and seek association with biochemical and haematological parameters linked to variability in refilling rates. Methodology: This study will attempt to describe variations in the plasma refill rate of prevalent dialysis patients during their normal haemodialysis treatment and during a session of 3 hours of haemodialysis preceded by 1 hour of isolated ultrafiltration using the in-built blood volume monitoring module of their haemodialysis machine and the TMON software that collects continuous, real-time data by interfacing with the computer network. To achieve this, a bolus of 100-300ml of intravenous dialysis replacement fluid will be administered at the beginning of each of the 2 studied sessions.

NCT ID: NCT03046784 Completed - Pregnancy Related Clinical Trials

Non-invasive Haemodynamic Monitoring in Pregnancy

Start date: January 2017
Phase:
Study type: Observational

This prospective and observational trial over 55 pregnant women (third trimester) compares non invasive haemodynamic monitoring using Nexfin technology and ultrasonography technic