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NCT ID: NCT04155879 Not yet recruiting - Atrial Fibrillation Clinical Trials

Atrial Fibrillation Recurrence Following Cardioversion: the Role of Clinical Factors and Alpha Defensin Levels

Start date: November 2019
Phase: N/A
Study type: Interventional

Atrial fibrillation and inflammation are strongly correlated. The aim of this study is to evaluate whether inflammation markers (alpha Defensin) predict maintenance of sinus rhythm following cardioversion. A secondary aim is to evaluate the role of Colchicine, an anti-inflammatory medication, in reducing the recurrence rate of atrial fibrillation.

NCT ID: NCT04151303 Not yet recruiting - Clinical trials for Respiratory Disease of A Newborn

The Optimal Timing for Cerclage Removal

Start date: December 1, 2019
Phase:
Study type: Observational [Patient Registry]

Women with a history of cervical insufficiency can be managed with elective cervical cerclage placed at the beginning of the second trimester. The McDonald technique is the most commonly used. Though lack a robust scientific evidence, the cerclage is removed electively at 36-37 weeks of gestation in order to avoid maternal cervical laceration. In addition, the incidence of spontaneous delivery is nearly 20% within 72 hours after ceclage removal, thus elective cerclage removal at 36-37 weeks may also put the newborns at complications associated with iatrogenic late preterm/early term delivery

NCT ID: NCT04150588 Not yet recruiting - Clinical trials for the Correlation Between Erin Test and Müller's Muscle-Conjunctival Resection

The Correlation Between MMCR and Phenylephrine Test

Start date: November 30, 2019
Phase:
Study type: Observational

The propose of the study is the examine the association between the amount that the eyelid rise 3 months after surgery and the reaction to Efrin test before surgery

NCT ID: NCT04140565 Not yet recruiting - Clinical trials for PET Images and Deep Neural Networks Algorithms

Positron Emission Tomography (PET) Images Using Deep Neural Networks

Start date: November 1, 2019
Phase:
Study type: Observational [Patient Registry]

PET images are based on detecting two annihilation 511 KeV photons that are produced by positron emitting isotopes. The longer the acquisition time, the more photons are detected and processed, resulting in better image quality. However, long scan times (typically 20-40 minutes per scan) are less convenient to patients, and may result in patient motion and misalignment. several studies have used machine learning to produce diagnostic images from low quality images.The goal of our study is to produce diagnostic PET images with 10 seconds acquisition time per bed position using DNN algorithms

NCT ID: NCT04101019 Not yet recruiting - Nerve Block Clinical Trials

Sphenopalatine Ganglion Block to Treat Shoulder Pain After Laparoscopic Surgery

Start date: September 2019
Phase: N/A
Study type: Interventional

This is a prospective double blinded randomized pilot trial to evaluate the efficacy of phenopalatine ganglion block (SPGB) block to manage shoulder tip pain (STP) after laparoscopic surgery. Patients undergoing laparoscopic surgery will be approached by a member of the research team and those found eligible for participating will be enrolled after signing an informed consent form. Patients will be randomized to have the SPGB block with saline versus active drug which contains 10% lidocaine diluted to 5%. The block will be performed , by an experienced member of the research team, and the patient will then be followed up by the investigator for any adverse events and levels of shoulder pain.

NCT ID: NCT04084821 Not yet recruiting - Delirium Clinical Trials

Estimation of Delirium Data Completeness

Start date: October 2019
Phase:
Study type: Observational

Currently physicians and nurses rely on their own clinical skills and experience to diagnose and record 'delirium' in the Electronic Health Records (EHR). This study aims to determine how delirium as a diagnosis is documented by clinicians in the EHR at Hadassah Hospital. The knowledge gained from this study will support the design of a better surveillance approach to monitoring delirium events in postoperative patients using electronic healthcare recorded data. There is considerable uncertainty surrounding the quality of 'delirium' records in the Electronic Health Records (EHR). The reliability of this chart estimation has become questionable in the absence of an objective definition of 'delirium' and a lack of highly accurate diagnostic tools in the hospital setting. Given the difficulty of accurately identifying delirium and the deficiency in the quality of EHR documentation, it is not surprising that delirium is grossly underestimated, undertreated, not properly recorded in the EHR or misreported. Data concordance plays a major role in documentation quality, especially for data-mining and knowledge extraction analysis, and therefore it is essential to address the reliability of 'delirium' labeled data within the EHR system.

NCT ID: NCT04080973 Not yet recruiting - Osteopenia Clinical Trials

Metabolic Workup in Patients Suffering From Kidney Stone Disease and Osteopenia

Start date: October 2019
Phase: N/A
Study type: Interventional

Patients suffering from acute renal colic are evaluated by non contrast computerized tomography with excellent identification rates of urinary stones. The scan also covers the bones of the ribs, spine and pelvis, allowing measurements of the bone density and identifying early osteopenic changes. Bone demineralization is associated with metabolic changes such as hypercalcemia or hypercalcuria. In this study the investigators will look for correlation between kidney stones, osteopenic bone changes and metabolic abnormalities.

NCT ID: NCT04080388 Not yet recruiting - Heart Failure Acute Clinical Trials

How to Prevent Heart Failure Readmission by Using Lung Impedance Device (HOPE-HF Study)

HOPE-HF
Start date: September 2019
Phase: Phase 3
Study type: Interventional

The readmission of Heart Failure (HF) patients for exacerbation HF within 30-day is unmet goal. The mail reason for readmission is excessive accumulation of fluid in patient's lung. According our data (1,2) around 40% of HF patient have excessive lung fluid at discharge from HF hospitalization ("unacceptable" residual congestion on discharge). In other words, around 40% patients are discharged from HF hospitalization prematurely when they are not ready to be discharged. Only 60% of HF patients are discharged from HF admission with "acceptable" level of residual pulmonary congestion (2). There are some techniques to assess "readiness" of HF patients for discharge. Pulmonary congestion (lung fluid accumulation) may be assessed non-invasively by measurement Brain Natriuretic Peptide (BNP), (3,4), by lung ultrasound (LUS), (5-7) and by Lung Impedance (LI) method (1,2). LUS is operator depended technique. LI and BNP techniques are most reliable methods (2) and easy to use.

NCT ID: NCT04074694 Not yet recruiting - Clinical trials for Parotitis, Juvenile Recurrent

Treatment of Juvenile Recurrent Parotitis: the Yield of Minimally Invasive Intervention

JRP
Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Juvenile recurrent parotitis (JRP) is an inflammatory disease characterized by recurrent painful swelling of the Parotid gland in the pediatric age. A watchful waiting treatment strategy was acceptable for most children; however, recent studies claimed that a sialoendoscopic intervention may stop the recurrent flare-ups. The Objective of our study: To determine the effectiveness of sialoendoscopy vs. conservative therapy ('watch and wait') alone for Juvenile Recurrent Parotitis Research Endpoints: The study's endpoints will evaluate frequency and severity of flare-ups before and after treatment and Quality of Life parameters as evaluated according to life-quality questionnaires.

NCT ID: NCT04032431 Not yet recruiting - Multiple Sclerosis Clinical Trials

Upper Limb Telerehabilitation With Virtual Reality in Multiple Sclerosis

TEAMS
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

This study aims to investigate the effectiveness of a home-based telerehabilitation program specifically designed for upper limbs, based on Virtual Reality (VR) in individuals affected by Multiple Sclerosis.