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NCT ID: NCT02323971 Recruiting - Clinical trials for Coronary Artery Disease

Impact of Renal Function on Ticagrelor-Induced Antiplatelet Effects in Coronary Artery Disease Patients

Ticagrelor
Start date: December 2014
Phase: N/A
Study type: Observational

Dual antiplatelet therapy consisting in aspirin and clopidogrel is the cornerstone of the treatment of the prevention of the thrombotic events in patients with coronary artery disease (CAD), showing a reduction in adverse events.

NCT ID: NCT02312583 Recruiting - Depression Clinical Trials

Efficacy of an Online Program for the Treatment of Mild and Moderate Depression

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

iFighDepression is an online self-help programme based on cognitive-behavioral therapy that could be useful for the treatment of mild to moderate depression

NCT ID: NCT02310555 Recruiting - Obesity Clinical Trials

Surgical Techniques in Diabetes Mellitus-II and Obesity. Metabolic Surgery Study (MSS)

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

The aim of this study is to compare clinical and laboratory findings of three surgical techniques in metabolic surgery in patients with type II diabetes mellitus and obesity (BMI> 30).

NCT ID: NCT02307383 Recruiting - Clinical trials for Bacterial Colonization

Pilot Study of the Effectiveness of Probiotics and Lactitol for the Decolonization of OXA-48 (Carbapenemase) Producing Klebsiella Pneumoniae Among Rectal Carriers

Start date: October 2014
Phase: Phase 2
Study type: Interventional

The combination of Lactitol and Probiotics (Lactobacillus acidophilus and Lactobacillus Biphidus) administered orally is an effective strategy of intestinal decolonization of Enterobacter produced OXA-48-type carbapenemase. The purpose of this study is to determine the effectiveness of Lactitol and Probiotics for the intestinal decolonization of people who carried Klebsiella pneumoniae produced OXA-48-type Carbapenemase.

NCT ID: NCT02306317 Recruiting - Clinical trials for Premature Birth of Newborn

The Adding Value of Parents to Nursing Care in the Control of FiO2

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

The purpose of this study is to determine whether saturation control by parents in children younger than 32 weeks or under 1500 g versus conventional care performed by nursing increases the time in which these patients remain at optimal saturation range. If the hypothesis of this study is confirmed premature infants could prevent episodes of hypoxia-hyperoxia and also give more relevance to the role of parents in caring for their children admitted in a neonatal intensive care unit.

NCT ID: NCT02297724 Recruiting - Clinical trials for Intrauterine Growth Restriction

MRI Assessment of Placental Health

Start date: April 2014
Phase:
Study type: Observational

The ultimate goal of this project is to develop methods that allow informed decision-making on the delivery time of fetuses that are at increased risk of stillbirth due to IUGR. In placenta related IUGR pregnancies, there can be multiple concurrent placental pathologies. Although there is no specific correspondence between a single type of pathology and IUGR, the common result of these pathologies is placental insufficiency, which limits the maternal-fetal exchange. Oxygen and nutrition transport is known to be hindered in IUGR placentas due to obstructed or abrupt vasculature, massive fibrin deposition, and inflammation in the villous and intervillous space (villitis). Thus one potential approach to distinguish IUGR pregnancies from normal ones is to assess the efficiency of placental transport. Based on the hypothesis that efficiency of oxygen transport is representative for overall oxygen and nutrition transport in placenta, the investigators propose to characterize the blood oxygenation and blood perfusion in placenta in vivo via MRI, and use it as an index for better stratification in the IUGR risk group. The investigators will also consider alternative MRI approaches such as structural, diffusion and spectroscopy measurements inside the placenta, which might reflect the state of placental transport and reveal the status of placental health. Specific aims: 1) To correlate the MRI metrics that differentiate placental insufficiency from normal placenta transport with histopathology data of the placenta. 2) To correlate the MRI metrics that reflects placental insufficiency with fetal outcome

NCT ID: NCT02291120 Recruiting - Clinical trials for Evaluate the Effects of MEDCEM PC and MTA in Pulpotomies of Primary Molars.

MEDCEM PC and MTA in Pulpotomies of Primary Molars

Start date: March 2014
Phase: Phase 4
Study type: Interventional

The objective of the study is to evaluate and compare, clinically and radiographically,the effects of MEDCEM PC and MTA when used as pulp dressings following pulpotomy in human primary molars.

NCT ID: NCT02284035 Recruiting - AIDS Clinical Trials

Safety & Efficacy of Dual Therapy With Raltegravir/Lamivudine

RALAM
Start date: January 2015
Phase: Phase 3
Study type: Interventional

A pilot 24-week open-label, randomized, controlled clinical trial to assess the safety, tolerability and efficacy of dual therapy with Raltegravir/Lamivudine combination when replacing standard combination therapy in HIV-infected patients with prolonged virological suppression

NCT ID: NCT02275286 Recruiting - Leiomyosarcoma Clinical Trials

Trabectedin Plus Radiotherapy in Soft Tissue Sarcoma Patients

TRASTS
Start date: November 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Phase I-II trial that combines trabectedin plus radiotherapy for tumor reduction response measure in four cohorts of patients: Cohort A: Patients with diagnosis of non-operable or unresectable or not oncologically recommended metastasectomy of limited to lung metastases soft tissue sarcoma. Cohort B: Patients with locally advanced resectable Myxoid Liposarcoma. Cohort C: Patients with retroperitoneal and resectable soft tissue sarcoma (liposarcoma and leiomyosarcoma). Cohort D (Phase II only): Patients with well differentiated liposarcoma and G2 dedifferentiated liposarcoma (with less than 30% dedifferentiated component). Phase I: escalating dose of 1.3 or 1.5 mg/m2. Phase I for cohort C: de-escalating dose of 1.5 or 1.3mg/m2 Radiotherapy for cohort A: 30Gy in 10 fractions (3Gy/fraction). Radiotherapy for cohort B: 45Gy in 25 fractions (1.8Gy/fraction). Radiotherapy for cohort C: 45Gy in 25 fractions (1.8Gy/fraction). Radiotherapy for cohort D: 45Gy in 25 fractions (1.8Gy/fraction). A translational substudy is developed to analyse different biomarkers predictive value. Cohorts A and B are closed to recruitment in 2023.

NCT ID: NCT02267239 Recruiting - Periodontitis Clinical Trials

Methodology Antiseptic Application, Influence on Oral Biofilm.

Start date: October 2014
Phase: Phase 4
Study type: Interventional

The study has the objective to compare two different methodology of application the antiseptic on the oral biofilm will be formed during 48h in situ on a specific device. The first one using the immersion in the antiseptic solution, as much of the authors did in the past. And the second way doing a active mouthwash, as the manufacturer recommends. The study will compare two different antiseptic solutions, the chlorhexidine (0.2% Oraldine Perio) and the essential oils (Listerine Mentol) with the two different application and compared the bacterial vitality, thickness and covering grade between solutions and with a basal sample.