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Hypotension clinical trials

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NCT ID: NCT03144817 Completed - Hypertension Clinical Trials

Dialysate Sodium Lowering Trial

DeSaLT
Start date: April 26, 2017
Phase: Phase 2
Study type: Interventional

This is a pilot randomized clinical trial in which patients treated with 3X per weekly conventional hemodialysis will be treated to a dialysate sodium 135 mEq/L vs. 138 mEq/L and followed for safety and tolerability, effects on BP and volume.

NCT ID: NCT03139123 Completed - Kidney Injury Clinical Trials

Prevalence of Hypotension Associated With Preload Dependence During Continuous Renal Replacement Therapy

PRELOAD-CRRT
Start date: May 18, 2017
Phase:
Study type: Observational

Per-dialytic hypotension is common in Intensive Care Unit patients under continuous renal replacement therapy, and occurs in nearly 50% of the patients. To date, there is a lack of study having characterized the underlying mechanism of hypotension in this setting. New diagnostic methods are now available with high reliability to identify hypovolemia as the underlying cause of hypotension, among which change in cardiac index during passive leg raising may be the less affected by restrictive validity criteria. A change in cardiac index greater than 10% during this test is highly predictive of preload dependence, i.e the probability than cardiac index will increase if cardiac preload increases. The aim of this study is then to identify, among hypotensive episodes occurring during renal replacement therapy in Intensive Care Unit patients, the percentage of episodes related to preload dependence as identified by passive leg raising.

NCT ID: NCT03136172 Completed - Hypotension Clinical Trials

Monitoring of Systemic or Organ Perfusion for Preterm Infants

Start date: May 8, 2017
Phase:
Study type: Observational

To investigate biomarker reflects systemic or specific organ perfusion well, we are going to the observational comparison study using several hemodynamic monitoring methods in the premature infants. It includes near-infrared spectroscopy (NIRS), pulse oximetry with perfusion index (PI) and pleth variability index (PVI) and functional echocardiography.

NCT ID: NCT03121092 Terminated - Hypertension Clinical Trials

ACEI/ARB Study in Ambulatory and Day of Surgery Admission Patients

ACE/ARB
Start date: May 16, 2012
Phase: N/A
Study type: Interventional

Angiotensin converting enzyme inhibitors (ACEI's) and Angiotensin receptor blockers (ARB's) are commonly used anti-hypertensive medications that may have implications on the management of a patient undergoing surgery. Limited research has looked at the effects of these medications on perioperative complications and mortality. Some studies conducted on small groups of inpatients with advanced vascular disease undergoing vascular surgery or coronary artery bypass grafting (CABG), suggest exacerbation of hypotension (low blood pressure) in patients who continued taking ACEI's or ARB's on the morning of their procedure. In addition, cases of low blood pressure (BP) that were refractory to standard treatment were reported. One recent retrospective study reported no difference in severe hypotension and only a modest difference in moderate hypotension managed by conventional treatment, but did not adequately address the risk of preoperative hypertension. A study recently published by the investigators (Twersky et al., 2014) in over 600 patients demonstrated no difference in preoperative hypertension in ambulatory surgery and same day admission patients. There has been limited data stratifying the degree of low BP based on severity but these were not done in ambulatory patients, and neither was the degree of high BP from discontinuing these medications addressed. As such, no uniform consensus has been reached and clinicians are unclear as to whether the reported inpatient findings are applicable to the outpatients, since they differ in many respects. The investigators propose to evaluate whether ACEI's and ARB's discontinued preoperatively have a negative impact on perioperative hemodynamics and patient outcome in a group of ambulatory and same day surgical patients. Similar to studies done on inpatients, the investigators will also evaluate patients receiving a standardized general anesthetic for hemodynamics following induction of anesthesia until surgical incision. The investigators hypothesize that continuing ACEI's and ARB's in the preoperative period does not result in an increased risk of severe hypotension (low blood pressure) following induction of general anesthesia.

NCT ID: NCT03113045 Recruiting - Clinical trials for Cesarean Section Complications

Seated Time for 90% Incidence of Hypotension

Start date: January 31, 2017
Phase: N/A
Study type: Interventional

The study will determine the 90% effective seated time after intrathecal injection of hyperbaric bupivacaine to avoid hypotension in patients undergoing cesarean delivery.

NCT ID: NCT03112070 Completed - Clinical trials for Postexercise Hypotension

Post-Exercise Hypotension After Water Exercise

Start date: April 4, 2016
Phase: N/A
Study type: Interventional

Hypertension is the most prevalent cardiovascular disease risk factor among individuals 60 years of age and older. Hypertension can be prevented and modified with lifestyle interventions that include regular exercise. Water exercise is widely recommended for older adults for a variety of health benefits, but few studies have assessed the immediate ambulatory blood pressure (BP) response to water exercise, a response termed postexercise hypotension (PEH). We will assess PEH after a session of water aerobics in physically active, older women with hypertension. Twenty-four women will be randomly assign to participate in a 45 min session of moderate intensity, water aerobics (WATER) and a 45 min land control session (CONTROL). All experimental sessions will start at 9 am sharply with 7 days between them. Subjects will left the experiments wearing an ambulatory BP monitor for the next 21 hr.

NCT ID: NCT03107598 Terminated - Hypotension Clinical Trials

Colloid Preload Versus Crystalloid Co-load in Cesarean Section Under Spinal Anesthesia

CPvsCC
Start date: March 2016
Phase: N/A
Study type: Interventional

Comparison between colloid preload and crystalloid co-load in cesarean section under spinal anesthesia. 1. The primary outcome was the incidence of hypotension 2. Secondary outcomes included the incidence of severe hypotension, total ephedrine dose, nausea and vomiting and neonatal outcome assessed by Apgar scores and umbilical artery blood gas analysis

NCT ID: NCT03106649 Recruiting - Hypotension Clinical Trials

Echocardiography Based Algorithm for Spinal Anaesthesia

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

The main aim of the study is to compare the proposed algorithm for preventing and treating spinal hypotension with normal anesthesia management of a spinal anesthesia. The proposed algorithm mainly will depend upon the left ventricular end diastolic area measurement by transthoracic echocardiography to assess the left ventricular preload status and its usefulness in preventing and treating spinal hypotension.

NCT ID: NCT03091881 Completed - Clinical trials for Spinal-induced Hypotension

Granisetron in Diabetic Parturients Decrease Spinal Induced Hypotension

Start date: March 1, 2018
Phase: Phase 4
Study type: Interventional

Diabetic Parturients are exposed to intraoperative hypotension after spinal anesthesia and we proposed that intravenous Granisterone 1 mg will attenuate the hypotension occurred with spinal block during Cesarean sections.

NCT ID: NCT03086694 Completed - Blood Pressure, Low Clinical Trials

Goal-Directed Fluid Therapy for Patients Undergoing Oro-Maxillofacial Surgery

Start date: April 5, 2017
Phase:
Study type: Observational

Orthognathic surgery, one kind of Oro-maxillofacial surgery, is a complicate surgery that undergoes several hours with nasotracheal intubation general anesthesia. To limit blood loss during operation, the patients are often under intentional hypotension. However, the intentional hypotension may confuse with hypovolemic induced low blood pressure. The hypothesis is using flotrac (to measure stroke volume variation) to keep the patients hemodynamics stable under Tridil and propofol infusion and avoid over-infusion of crystalloid or colloid and prevent hypovolemia induced postoperative nausea and vomiting.