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NCT ID: NCT03053193 Recruiting - Breast Cancer Clinical Trials

MammaPrint, BluePrint, and Full-genome Data Linked With Clinical Data to Evaluate New Gene EXpression Profiles

FLEX
Start date: April 28, 2017
Phase:
Study type: Observational [Patient Registry]

The FLEX Registry will be implemented to operate as a large-scale, population based, prospective registry. All patients with stage I to III breast cancer who receive MammaPrint® and BluePrint testing on a primary breast tumor are eligible for entry into the FLEX Registry, which is intended to enable additional study arms at low incremental effort and cost. FLEX Registry will utilize an adaptive design, where additional targeted substudies and arms can be added after the initial study is opened.

NCT ID: NCT03047681 Recruiting - Clinical trials for Transcatheter Aortic Valve Implantation Prosnosis and Complications

Tryptase Level as a Marker of Complications in Transcatheter Aortic Valve Replacement

TAVR
Start date: February 2017
Phase: N/A
Study type: Observational

An association between mast cells and outcomes of patients undergoing transcatheter aortic valve replacement (TAVR) has not been studied to our knowledge. We aim to characterize tryptase levels dynamics during TAVR; Demonstrate whether tryptase level post-TAVR can be used as a prognostic marker.

NCT ID: NCT03047122 Recruiting - Ultrasonography Clinical Trials

Detection of Breast Lesions by Automatic Breast US

Start date: March 1, 2017
Phase: N/A
Study type: Observational

Mammography is considered the standard imaging method for breast cancer screening, and is known to result in reduced mortality from breast cancer. However, the diagnostic yield of mammography depends particularly on breast tissue density, with sensitivity as low as 30-48% in dense-breast women. Ultrasound is an attractive adjunct imaging method to mammography as it is widely accessible, relatively inexpensive and well-tolerated by patients. The addition of hand-held ultrasound to mammography has been demonstrated to significantly increase breast cancer detection in women with dense breasts. It is however dependent on the expertise and skill of the operator. In recent years, the FDA has approved the use of the automated breast ultrasound (ABUS) for use in screening of women with dense breast. Unlike handheld ultrasound, the ABUS is relatively simple to use, necessitating less technical training, and results in higher reproducibility. The research aim is to evaluation of automated breast ultrasound (ABUS) regarding the detection and classification of breast lesions, compared to hand-held ultrasound, according to the American College of Radiology Breast Imaging-Reporting and Data System (BI-RADS) classification. The investigator will also evaluate parameters regarding patients' comfort, workflow, and duration of image interpretation.

NCT ID: NCT03046511 Recruiting - Clinical trials for Peritoneal Dialysis Complication

Peritonitis Prevention After Insertion of Peritoneal Dialysis Catheter.

Start date: March 8, 2017
Phase: Phase 3
Study type: Interventional

An intraperitoneal implanted catheter is always necessary to perform Peritoneal Dialysis. Catheter insertion has been associated with infectious complication such as Exit Site Infection (ESI), Tunnel Infection and Peritonitis. The last one may lead to loss of the technique because the need of catheter removal. Most of international guidelines recommends the use of prophylactic antibiotics. Different protocols has been used, mostly intravenous single injection before the procedure. For the last 25 years our unit gives a single intraperitoneal dose of Cefazolin immediately after the catheter insertion. The aim of this study is compare the effect of a pre- operative IV dose os Cefazolin with a post- procedure intraperitoneal single dose administration of the same drug.

NCT ID: NCT03045939 Recruiting - Induction of Labor Clinical Trials

Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours

DoubleCRIB
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

This study will evaluate the insertion of double balloon device (DBD) for cervical ripening for 12 h vs 6 hours.

NCT ID: NCT03044093 Recruiting - Clinical trials for Second Trimester Abortion

Mifepristone and Misoprostol Compared With Misoprostol Alone for Second Trimester Abortion

Start date: January 2017
Phase: Phase 4
Study type: Interventional

Mifepristone and Misoprostol Compared With Misoprostol Alone for Second Trimester Abortion - a Double Blinded Randomized Controlled Trial

NCT ID: NCT03041922 Recruiting - Clinical trials for Changes in Elasticity Duo to Pressure Ulcers in Buttocks

Estimation of Changes in Soft Tissue Rigidity of the Buttocks in Sitting Under Weight Bearing Compared to Sitting Without Weight Bearing

Start date: March 1, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Estimation of Changes in Soft Tissues Elasticity in Buttocks in lying down and sitting positions by using ultrasound device. the elasticity of fat and muscle tissues will be measured. May ultrasound exam helps to predict the development of pressure ulcers in buttocks due to continuous sitting.

NCT ID: NCT03037801 Recruiting - Bronchiolitis Clinical Trials

Intrapulmonary Percussive Ventilation for Children With Bronchiolitis on Non-Invasive Ventilation Support

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Prospective randomized study of patients admitted to the Pediatric Intensive Care Unit suffering from Bronchiolitis and are supported on Non Invasive Positive Pressure Ventilation. The patient population will be divided into two groups, one group will receive conventional treatment and the other group will receive conventional treatment and three times a day of physiotherapy using Intrapulmonary Percussive Ventilation.

NCT ID: NCT03036254 Recruiting - Diabetes Mellitus Clinical Trials

Hyperbaric Oxygen Therapy for Cognition in Diabetic Elderly at High Dementia Risk

Start date: October 8, 2017
Phase: N/A
Study type: Interventional

An urgent need exists to identify effective interventions to arrest or reverse dementia and cognitive loss at its earliest stages. The proposed pilot randomized clinical trial will investigate the short and long-term effects of hyperbaric oxygen therapy on cognitive functioning, cerebral blood flow, and glucose uptake in diabetic elderly with mild cognitive impairment. and provide the basis for a large-scale multi-center study of hyperbaric oxygen therapy effects on cognition in diabetes. The potential to preserve, or even enhance, cognition in elderly at high risk of cognitive decline and dementia has major implications for the affected individuals and their support systems that bear the social and financial burdens of long-term caregiving.

NCT ID: NCT03034031 Recruiting - Clinical trials for TBI (Traumatic Brain Injury)

MR Imaging Study of TBI in Children

MISTIC
Start date: June 24, 2018
Phase:
Study type: Observational

This project will combine the data collected from structural and functional MRI scans and neuropsychology performance post-TBI in children. Patients will be followed for a year, in order to examine the brain and cognitive recovery post head injury.