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Chest Pain clinical trials

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NCT ID: NCT04313465 Withdrawn - Clinical trials for Acute Coronary Syndrome

T-MACS Decision Aid: a Randomized, Controlled Point of Care Trial

Start date: January 2021
Phase: N/A
Study type: Interventional

The aim of the study is to establish whether the safety of the T-MACS decision aid to immediately 'rule out' acute coronary syndromes with one blood sample for the cardiac damage marker troponin, is non-inferior to an approach requiring serial troponin sampling over three hours.

NCT ID: NCT03961048 Withdrawn - Pain, Postoperative Clinical Trials

Ideal Initial Bolus and Infusion Rate for Erector Spinae Plane Block Catheters

Start date: July 23, 2019
Phase: Phase 4
Study type: Interventional

This study would like to identify the best starting dose and infusion rate for nerve blocks and nerve catheters related to the erector spinae plane block that can improve functional status and pain control on cardiac surgery patients and minimize the necessity for opioid pain control using a continuous reassessment model.

NCT ID: NCT03906812 Withdrawn - Chest Pain Clinical Trials

A Randomized Trial of Telemetry Compared With Unmonitored Floor Admissions in ED Patients With Low-Risk Chest Pain

Start date: September 2020
Phase: N/A
Study type: Interventional

This study aims to determine, relative to telemetry admission, if admission to an unmonitored floor bed saves resources without an increased rate of adverse events in emergency department (ED) patients admitted with chest pain and low-risk features.

NCT ID: NCT03874806 Withdrawn - Pain, Postoperative Clinical Trials

Pharmacokinetic Profile and Dermatomal Coverage of the Erector Spinae Plane Block

Start date: July 1, 2019
Phase: Phase 4
Study type: Interventional

The goals of this study are as follows: 1. to confirm the safe dosing of ropivacaine for the erector spinae plane block 2. develop a pharmacokinetic profile of the erector spinae plane block, which will help demonstrate how quickly and how closely toxic levels are reached when a routine dose of ropivacaine is given for this nerve block 3. assess numbness created by the erector spinae block when routine doses are administered

NCT ID: NCT02828761 Withdrawn - Chest Pain Clinical Trials

Coronary Calcium Scoring Versus Standard Care for Emergency Department Chest Pain Patients

Start date: July 2023
Phase: N/A
Study type: Interventional

This research asks whether coronary calcium scoring, a non-invasive test based on computed tomography scanning, is a better way to diagnose chest pain patients than other currently used methods. Three of four patients will undergo calcium scoring and the remaining patients will receive standard care.

NCT ID: NCT02569073 Withdrawn - Esophageal Diseases Clinical Trials

Investigation of Cannabinoid Receptor Agonist Dronabinol in Patients With Functional Chest Pain

ICAMP
Start date: June 21, 2017
Phase: Phase 4
Study type: Interventional

In a recent study, Dronabinol was shown to reduce symptoms in patients with Functional Chest Pain (non-cardiac chest pain). Additionally, metabolic measures and patients' weights were not adversely affected by this regiment. In fact, some cholesterol measures trended in a favorable direction with Dronabinol. The study lasted 28 days and patients took Dronabinol twice daily. The goal of this current study focuses on reducing the dose of Dronabinol to see if the same goals can be achieved. More so, the study will be extended to 12 weeks to gain a more longitudinal picture of therapy with Dronabinol. It is hypothesized that reducing the dose and extending the duration will continue to show an improvement in symptoms as well as no adverse metabolic outcomes.

NCT ID: NCT02330328 Withdrawn - Clinical trials for Acute Coronary Syndrome

Telemetry for Chest Pain of Low Risk for Acute Coronary Syndrome Pts

Start date: April 2015
Phase: N/A
Study type: Interventional

This is a randomized controlled, multi-center, non-blinded non-inferiority study examining the utility of telemetry monitoring in patients admitted who are low risk for acute coronary syndrome. Each of the six sites will prospectively enroll 250 patients in each arm of the study randomized to either a med-surg bed (no telemetry) or a telemetry bed during their admission. Research study coordinators will enroll patients and then follow them throughout their hospital course and record primary and secondary end point events.

NCT ID: NCT02158754 Withdrawn - Clinical trials for Coronary Artery Disease

Clinician Utilization of Corus CAD (or ASGES) in Primary Care Provider Decision Making

CU-PCP
Start date: May 2014
Phase:
Study type: Observational

This retrospective study will investigate clinician behavior in diagnosing patients with possible obstructive coronary artery disease who received a Corus CAD (Age/Sex/Gene Expression score - ASGES) result compared to patients who did not have the test performed (matched control patients).

NCT ID: NCT01637571 Withdrawn - Chest Pain Clinical Trials

Dexilant Treatment in Gastrointestinal Reflux Disease (GERD Related Non Cardiac Chest Pain

Dexilant
Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate a new treatment for non-cardiac chest pain (NCCP) related to gastrointestinal reflux disease (GERD), called Dexilant. The investigators would like to test its effectiveness in treating NCCP. The patient will undergo esophageal balloon distention testing (EBDT) before and after taking the new treatment for one month (Dexilant). EBDT evaluates the sensation and mechanical properties of the esophagus. A catheter with a deflated balloon is placed through the mouth and into the esophagus and the balloon is inflated with water. ECG and labs will be done throughout the study as a measurement of safety.

NCT ID: NCT01562964 Withdrawn - Chest Pain Clinical Trials

Hypnotherapy in Patients With Chest Pain & Unobstructed Coronaries

Start date: February 1, 2012
Phase: N/A
Study type: Interventional

This study will investigate whether clinical hypnotherapy can effectively treat chest pain symptoms, improve emotional wellbeing and quality of life in postmenopausal women with chest pain and coronary arteries without any narrowings. The diagnosis of chest pain with 'normal' coronary arteries is found in 25% of patients undergoing investigation of chest pain using coronary angiography (when dye is injected into the coronary arteries whilst xray pictures are taken), and the majority of these patients are postmenopausal women. Often there is no obvious physical cause. Despite symptoms being treated using conventional drugs, and life expectancy is not affected, many patients continue to suffer from debilitating chest pain symptoms, frequently resulting in visits to hospital, increased psychological illness and poor quality of life. The investigators are interested in finding ways of improving not only chest pain symptoms but also psychological wellbeing and quality of life in these patients. Previous studies of ours have found improvement in these patients after taking part in a support group, and using a relaxation technique called Autogenic training. Recently the investigators conducted a pilot study which showed a favourable effect of hypnotherapy on physical ability, well-being and quality of life. The investigators would now like to extend this study, performing a larger randomised, controlled trial. The investigators hypothesise that hypnotherapy will beneficially affect symptoms and quality of life in patients with cardiac Syndrome X.