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NCT ID: NCT02445222 Recruiting - Clinical trials for Long Term Safety of Patients Receiving CAR-T in an Eligible Clinical Trial or Managed Access Program

CAR-T Long Term Follow Up (LTFU) Study

PAVO
Start date: November 2, 2015
Phase: Phase 3
Study type: Interventional

Per Health Authorities guidelines for gene therapy medicinal products that utilize integrating vectors (e.g. lentiviral vectors), long term safety and efficacy follow up of treated patients is required. The purpose of this study is to monitor all patients exposed to CAR-T therapied for 15 years following their last CAR-T (e.g. CTL019) infusion to assess the risk of delayed adverse events (AEs), monitor for replication competent lentivirus (RCL) and assess long-term efficacy, including vector persistence.

NCT ID: NCT02440802 Recruiting - Prostate Cancer Clinical Trials

Evaluation and Predictive Value of Genetic Polymorphisms in the Management of Hormonal Treatment of Prostate Cancer

Feel+
Start date: April 2013
Phase: N/A
Study type: Observational

Androgen deprivation therapy (ADT) by surgical castration or administration of LHRH agonists or antagonists is the gold-standard systemic treatment of Prostate Cancer. The efficacy, severity and frequency of side effects of ADT vary from a patient to another. The exact cause of this variability is not known, however certain genetic polymorphisms affecting enzymes implicated in the synthesis and metabolism of sex-steroids seem to be involved in these processes. To perform a longitudinal study to evaluate the prevalence of various genetic polymorphisms affecting genes in the sex-steroid synthesis and metabolism pathway (CYP1A1, CYP1B1, CYP19A1, 17HSD, HSD3B1, AR, ESR1, ESRRG, IL6, TNF-alpha) in men with Prostate Cancer receiving ADT and the possible association between polymorphisms and frequency and severity of side-effects of ADT.

NCT ID: NCT02440763 Recruiting - Clinical trials for Spinocerebellar Ataxia

The EUROSCA Natural History Study

EUROSCA-NHS
Start date: July 2005
Phase: N/A
Study type: Observational

The key goals of EUROSCA-NHS is to determine and compare the rate of disease progression in SCA1, SCA2, SCA3 and SCA6 including determination of the order and occurrence of non-ataxia symptoms, assessment of activities of daily living (ADL) and quality of life (QoL), and identification of predictors of disease progression and survival.

NCT ID: NCT02434198 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Falling in Patients With COPD Referred to Pulmonary Rehabilitation: Incidence, Risk Factors and Prediction Tools

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

The primary aim of this study is to investigate the incidence of falling in a cohort of patients with chronic obstructive pulmonary disease (COPD) referred to a pulmonary rehabilitation program and to verify the risk factors. The secondary aim is to verify whether available balance assessment tools are feasible in clinical practice and which tools and values can best predict falls in people with COPD.

NCT ID: NCT02430740 Recruiting - Infertility Clinical Trials

Tailored Ovarian Stimulation Based on BMI, AMH, AFC

Start date: January 2016
Phase: Phase 4
Study type: Interventional

The study objective is to develop a tailored based strategy for ovarian stimulation in IVF patients using AMH, BMI, antral follicle count (AFC). 300 patients will be randomized in 2 arms: 1. control group: standard care rec FSH. 2. study group: modified dose of Rec FSH based on AFC with a correction factor based on BMI and basal AMH level. Primary endpoints: number of mature follicles and eggs collected at egg retrieval; amount of rec FSH used. Secondary endpoints: fertilization rate; cleavage rate; clinical pregnancy rate; inhibin B and AMH levels during ovarian stimulation.

NCT ID: NCT02429531 Recruiting - Clinical trials for Specific Polysaccharide Antibody Deficiency

Polysaccharide Antibody Response Study

PARS
Start date: October 2015
Phase: Phase 4
Study type: Interventional

Specific polysaccharide antibody deficiency (SPAD) is a primary immunodeficiency characterized by a deficient antibody production to capsular polysaccharides with normal total immunoglobulin levels. Patients suffer from recurrent ear-nose and throat infections and lung infections. SPAD can also occur as part of a primary immunodeficiency affecting other components of the immune system. Diagnosis of SPAD is hampered by difficulties with the interpretation of the Pneumovax 23 antibody response. The purpose of this study is to assess the diagnostic value of the Typhim Vi antibody response and allohemagglutinin titers as an alternative to the Pneumovax 23 response to detect polysaccharide specific antibody deficiency.

NCT ID: NCT02425774 Recruiting - Postoperative Ileus Clinical Trials

Anti-inflammatory Effect of Pre-operative Stimulation of the Cholinergic Anti-Inflammatory Pathway

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

Hypothesis: Prucalopride can mimic electrical stimulation of the abdominal vagus nerve and has an anti-inflammatory effect. Aims: In the present pilot study, the investigators want to evaluate the anti-inflammatory effect of prucalopride. The following aims are formulated: 1. to show that prucalopride has a similar inflammatory effect as abdominal vagus nerve stimulation (VNS) 2. to evaluate whether prucalopride leads to accelerated post-operative recovery

NCT ID: NCT02425540 Recruiting - Clinical trials for Undetermined Ovarian Mass

Characterization of Ovarian Masses Unable to Classify With Gynecological Ultrasonography: Value of Pelvic MRI With Perfusion- and Diffusion-weighted Imaging

IOTAMRI
Start date: March 2015
Phase: N/A
Study type: Observational

The aim of the study is to prospectively evaluate the value of pelvic MRI including diffusion- and perfusion-weighted sequences in the selected group of patients that have an undetermined ovarian mass at ultrasound.

NCT ID: NCT02424981 Recruiting - Healthy Clinical Trials

Efficiency of Inspiratory Muscle Training in Elderly People

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

Efficiency of inspiratory muscle training in elderly people. Outcomes are lung function, muscle strength and chest expansion.

NCT ID: NCT02421705 Recruiting - Healthy Controls Clinical Trials

Visceral Sensitivity in IBD (Irritable Bowel Disease) and IBS (Irritable Bowel Syndrome)

Start date: February 2010
Phase: N/A
Study type: Interventional

Aim: More insight in pathogenesis of IBS and IBD. Samples are collected in context of an European research project.