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Systolic Murmurs clinical trials

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NCT ID: NCT06105866 Enrolling by invitation - Clinical trials for The Relationship Between TAPSE Value and Volume

Relationship of Preoperative Fasting With Tricuspid Annular Plane Systolic Excursion

(TAPSE)
Start date: February 11, 2024
Phase:
Study type: Observational

The aim of our study is to try to establish a relationship between preoperative fasting-related volume changes and tricuspid annular plane systolic excursion (TAPSE), and to determine whether there are changes in right ventricular functions due to preoperative fasting.

NCT ID: NCT05874687 Enrolling by invitation - Hypotension Clinical Trials

Tricuspid Annular Plane Systolic Excursion to Predict Arterial Hypotension Caused by Spinal Anesthesia in Caesarean Section

CESERAN TAPSE
Start date: June 1, 2023
Phase:
Study type: Observational

This cross-sectional blinded study was planned to be conducted in Aydın Gynecology and Pediatrics Hospital between June 2023 and September 2023. The study was designed for adult pregnant female cases between the ages of 20 and 35. Patients with Class II American Society of Anesthesiologists (ASA) physical status, scheduled for elective cesarean section under subarachnoid block and who gave informed consent were planned to be included in the study. Patients with emergencies and uncontrolled systemic comorbidities (e.g., cardiovascular, respiratory or renal) and patients with expected massive intraoperative loss (i.e., placenta accreta or placenta previa) are planned to be excluded from the study. Also, cases receiving intravenous fluid preload will be excluded.

NCT ID: NCT03984591 Enrolling by invitation - Clinical trials for Systolic Heart Failure

A Registry-based Cluster Randomized Trial to Compare the Effect of Spironolactone vs. Eplerenone on Clinical Outcomes in Patients With Symptomatic Systolic Heart Failure

CROWD-ASPECT
Start date: November 1, 2020
Phase: Phase 4
Study type: Interventional

Objective The objective is to compare the efficacy of spironolactone and eplerenone on clinical outcome in patients with heart failure and a reduced ejection fraction. Method The study is a crossover cluster randomized trial. Each heart failure clinic in Denmark will be allocated to four periods (clusters): two periods with spironolactone and two periods with eplerenone as first drug. The planned total participation time for each department is 4 years and we estimate that data from 7200 patients will be accrued in this period. Endpoints will be assessed through Danish National Registries.