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NCT ID: NCT02191436 Recruiting - Haemophilia Clinical Trials

Adherence to Treatment in Hemophilia

ADHERENCE
Start date: May 2015
Phase: N/A
Study type: Observational [Patient Registry]

Psychosocial factors and adherence to treatment in patients with hemophilia. A multicenter study. Multicenter cross sectional study of patients with hemophilia and their families

NCT ID: NCT02189369 Recruiting - Infertility Clinical Trials

Diagnostic Test for Endometrial Receptivity 24 Hours Before Embryo Transfer

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

This clinical validation study is being carried out to validate the efficacy of a test measuring the clinical application of prostaglandins present in the endometrial fluid in patients, 24 hours before the embryonic transfer. This test is capable of predicting endometrial receptivity without the need of performing a biopsy.

NCT ID: NCT02187874 Recruiting - Clinical trials for Postpartum Haemorrhage

Timing of Umbilical Cord Occlusion in Premature Babies( <33 w). Delayed vs Early.

CODE-P
Start date: July 2014
Phase: N/A
Study type: Interventional

Early cord clamping after delivery has been common practice for many decades as part of the active management of the third stage of labour. However in recent years, several studies have shown that delayed cord clamping may offer important benefits to the newborn. The data gathered indicate that delayed cord clamping may be particularly useful in premature babies, between 26 and 32 weeks of gestational age, reducing the need for blood transfusion and the incidence of intraventricular haemorrhage. However it is argued that the described potential benefits of delayed cord clamping could be negated by the increased risk of polycythaemia and jaundice in the newborn, as well as by potential interference with the postpartum haemorrhage management, initial care and reanimation of the premature newborn, and the possibility of cord blood donation. These factors, together with as the lack of homogeneity among existing studies regarding the delayed cord clamping technique create the need, in our opinion, for further research, to establish the proper place of this measure. Our hypothesis is that delayed cord clamping in the premature newborn significatively reduces the need for blood transfusions and intraventricular haemorrhage, compared with usual early cord clamping. Secondary outcomes: - To define the impact of delayed cord clamping on neonatal assessment parameters after delivery: APGAR score, cord pH, need for mechanical ventilation or reanimation. - Neonatal mortality and morbidity - Effect of the procedure on the incidence and severity of maternal postpartum haemorrhage - To study the correlation between Iron metabolism and reticulocitary haemoglobin levels in cord and infant blood.

NCT ID: NCT02187432 Recruiting - Clinical trials for Autosomal Dominant Polycystic Kidney Disease

The Eurocyst Initiative: Building a Network of ADPKD Reference Centers Across Europe

Start date: August 2013
Phase: N/A
Study type: Observational

EuroCYST initiative aims to build a large, well-characterized cohort of Autosomal Dominant polyCYSTic Kidney Disease (ADPKD) subjects who are followed in a longitudinal observational cohort study has the potential to identify progression factors and biomarkers, and to assess disease stage specific mortality, morbidity and health care costs.

NCT ID: NCT02186613 Recruiting - Breast Feeding Clinical Trials

Telephone Support From Primary Care for Breastfeeding Mothers

Start date: October 2014
Phase: N/A
Study type: Interventional

The investigators will conduct a telephone-based support to breastfeeding women with healthy newborns to improve breastfeeding outcomes.

NCT ID: NCT02163642 Recruiting - Bronchiectasis Clinical Trials

Role of Innate Immunity in Non-Cystic Fibrosis Bronchiectasis

Start date: April 2014
Phase: N/A
Study type: Observational

The purpose of this study is to demonstrate that 1) the secretion of mucins, antimicrobial peptides and Toll-like receptors is altered in certain patients with non-CF bronchiectasis, which makes them more susceptible to be infected by potentially pathogenic bacteria (PPB); and 2) the electronic nose is able to detect patterns of specific Volatile Organic Compounds (VOC) for patients with non-CF bronchiectasis colonized by PPB.

NCT ID: NCT02158923 Recruiting - Clinical trials for Moderated-high Risk of Postoperative Pulmonary Complication

Individualized Perioperative Open Lung Ventilatory Strategy

iPROVE
Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether individualized ventilatory management combining the use of low tidal volumes, alveolar recruitment maneuvers, individually titrated positive end-expiratory pressure and postoperative individualized ventilatory support will decrease postoperative complications, unplanned ICU readmissions, ICU and hospital length of stay and mortality compared to a standardized Lung Protective Ventilation (LPV) for all patients at risk.

NCT ID: NCT02144545 Recruiting - Obesity, Morbid Clinical Trials

Impact of Size of Gastric Sleeve on the Weight Loss. Correlation With Gastric Function and Endocrine-metabolic Changes.

Start date: October 2013
Phase: N/A
Study type: Interventional

Morbid Obesity (MO) is considered the most important epidemic in the developed world in the twenty-first century. After initial assessment of morbidly obese patients and the exclusion of potentially correctable causes, management involves a combination of dietary changes, cognitive therapy, physical activity, psychological support and pharmacological treatment. However, any combination of these factors has proven long-term effectiveness in achieving significant and sustained reduction of excess weight. Currently, surgery is the only treatment capable of achieving this goal, interacting also with significant improvement in quality of life and overall long-term mortality. In recent years, several authors have reported excellent short-term results with performing sleeve gastrectomy, but whether some aspects regarding the variability of gastric tubulization design could influence the results obtained in relation to weight loss and functional changes and gastric hormones. The main objective of this study is to assess the size of the gastric tubulization (based probe calibration and the distance from the pylorus to which initiate gastric section) that can provide a better clinical outcome (such as excess weight loss) in patients undergoing surgery for morbid obesity. Secondary objectives were to assess the morphological changes, physiological and hormonal obtained according to the size of the gastric tubulization and its effect on weight loss patients.

NCT ID: NCT02144116 Recruiting - Fibromyalgia Clinical Trials

Dance-movement Therapy Programme in Fibromyalgia.

Start date: May 2014
Phase: N/A
Study type: Interventional

Fibromyalgia is a chronic illness characterized by persistent widespread muscle pain with generalized hyperalgesia and allodynia. It can be accompanied by other concomitant symptoms like fatigue, sleep disturbances, musculoskeletal disorders, distress and psychological disorders. This condition is very prevalent. It has been reported to be about 2-5% of the general global population. Fibromyalgia is associated with balance problems and increased fall frequency. The objective of this study was to examine the effects of an 8 weeks dance-movement therapy programme on balance, strength, flexibility and quality of life in patients with fibromyalgia.

NCT ID: NCT02143336 Recruiting - Colorectal Surgery Clinical Trials

Subcuticular Continuous Suture Versus Skin Staples to Reduce Surgical Site Infections in Colorectal Surgery Patients

Start date: September 2013
Phase: N/A
Study type: Interventional

A comparison of skin closure techniques (standard skin closure with staples versus a continuous (subcuticular) absorbable suture), to determine if this changes the rate of post operative wound infections in elective colorectal surgery patients.