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NCT ID: NCT03776656 Completed - Clinical trials for Adenylosuccinate Lyase Deficiency

Evaluation of a Treatment With Allopurinol in Adenylosuccinate Lyase Deficiency

ADSL
Start date: October 14, 2019
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate the effectiveness of allopurinol treatment at 12 months on the adaptive and cognitive functioning of patients with adenylosuccinate lyase deficiency (ADSL). The psychiatric evaluation will involve the use of standardized tools prior to initiation of treatment, and will be repeated 6 months and 12 months after the start of treatment. The decrease in the concentration of SAICAR and S-Ado metabolites, which are markers of adenylosuccinate lyase (ADSL) deficiency, will also be quantified. Similarly, the efficacy of allopurinol on epileptic seizures for epileptic patients and on electrocardiogram abnormalities will be evaluated secondarily

NCT ID: NCT03776643 Completed - Clinical trials for With a Positive Skin Prick Test to Birch Pollen

Safety and Efficacy of Low-dose IL-2 in Birch Pollen Allergy

Rhinil-2
Start date: February 1, 2019
Phase: Phase 2
Study type: Interventional

Several studies have reported a deficit and/or a defect in regulatory T cells in allergic subjects, which can be correlated with the allergic responses, especially for respiratory allergies. Low-dose IL-2 (ld-IL2) specifically targets and activates regulatory T cells (Tregs), which are cells that regulate immune responses. Thus by stimulating Tregs, ld-IL2 would control allergic responses. This study is designed to evaluate the efficacy of ILT-101 (ld-IL-2), compared to placebo, on the nasal response assessed by Total Nasal Symptom Score (TNSS) during a controlled birch allergen exposure.

NCT ID: NCT03776565 Completed - Pregnancy Related Clinical Trials

Comparison of Antrum Surface Between Women With Operative Hysteroscopy or Planned Caesarean Section

ECHOCESAR
Start date: November 26, 2018
Phase:
Study type: Observational

Realization of a gastric ultrasound just before surgery, to measure the surface of antrum of stomach and compare if divergence sizes can be observed between women with a operative hysteroscopy and women with a planned caesarean section. To know if anaesthesia need to be adapted to the population.

NCT ID: NCT03776214 Completed - Clinical trials for Optimal Treatment of Lymphedema

Surgery in Addition to the Medical Treatment of Lymphedema

LYMPHOSPIR
Start date: April 1, 2018
Phase:
Study type: Observational

Lymphedema is a chronic pathology with a real impact on the quality of life of patients. Despite optimal medical management of patients, some patients still have no pitting edema on which the medical treatment has no effect. It is adipose tissue secondary to the evolution of lymphedema. It is often painful and important in terms of volume with the resulting functional consequences. The investigators propose to these patients a surgical management complementary to the optimal medical treatment by microlipoaspiration associated or not with a dermolipectomy. This surgical management began in 2014 in our service. The investigators want to evaluate the impact on quality of life of patients in this surgical management in addition to medical care.

NCT ID: NCT03775863 Completed - Clinical trials for Liver Transplant Disorder

AFP Model and Liver Transplantation.

Start date: November 11, 2017
Phase:
Study type: Observational

Background & Aim: Presence of microvascular invasion (mvi) in the explanted liver defines a higher risk of recurrence of hepatocellular carcinoma (HCC) after liver transplantation (LT). The aim of this study is to evaluate pre LT selection models of HCC recurrence specifically in patients without mvi in the explanted liver. Methods: Three multicenter cohorts are going to be included: a Latin American, a French and an Italian cohort of consecutive adult patients with HCC a first LT performed during two different periods: 2005-2011 and 2012-2016. AFP model is going to be compared against Milan and San Francisco criteria according to each models accuracy and prediction of HCC recurrence among patients without microvascular invasion in the explanted liver considering these candidates as "Low-risk patients". Multivariate Cox regression analysis, with hazard ratios (HR) and 95% confidence intervals (CI) for 5-year recurrence is going to be done with Competing Risk Regression analysis and corresponding Subhazard Ratios (SHR).

NCT ID: NCT03775564 Completed - Schizophrenia Clinical Trials

Effectiveness of the RemedRugby Program

RemedRugby
Start date: November 2014
Phase: N/A
Study type: Interventional

REMEDRUGBY's objective is to strengthen the capacity of users to interact with others in an assertive way and to fight against stigma. It proposes to specifically target the processes of "social cognition". "Social cognition" brings together the mental mechanisms that allow everyone to decipher the social situations, emotions and intentions of others and interact with others in the different contexts of everyday life. People with a psychic handicap frequently have difficulties in this area, which has often important consequences for their social and professional integration. The REMEDRUGBY program proposes to work specifically on these processes in the context of sport (+ role Play and blog) to strengthen the ability to interact with others and to deal with the stigma that can be encountered on a daily basis.

NCT ID: NCT03775304 Completed - Quality of Life Clinical Trials

Evaluation of End of Life Quality of Care

EFIQUAVIE
Start date: January 1, 2011
Phase:
Study type: Observational

The study uses a mixed method study to evaluate wether the use of the indicators of the Quality of end-of-life cancer care, developed by Earle et al [Earle JCO 2003; DOI: 10.1200/JCO.2003.03.059] would be relevant and measurable in France. The qualitative part of study was designed to investigate the representations of quality by face-to face interviews with family carer of recently deceased cancer patients, and with their oncologists, and nurses. The quantitative part of the study, consisted in a decedents case series analysis, diagnosed with advanced cancer and followed up in 5 centers. Data on trajectory of care were collected from different complementary sources associating national mortality data, hospital activity data, and health records. The study was approved by the French data protection authority (CNIL) number 611273.

NCT ID: NCT03774875 Completed - Psoriasis Clinical Trials

A Study of the Impact of Apremilast (CC-10004) on Quality of Life, Efficacy, and Safety in Adults With Manifestations of Plaque Psoriasis and Impaired Quality of Life

EMBRACE
Start date: March 28, 2019
Phase: Phase 4
Study type: Interventional

The primary objective of the study is to assess the impact of treatment with apremilast 30 mg twice daily for 16 weeks, compared to placebo, on health-related quality of life (QOL) in adults with manifestations of plaque psoriasis and impaired quality of life.

NCT ID: NCT03774576 Completed - Healthy Volunteers Clinical Trials

A Study to Investigate the Effect of CYP3A Inhibition on the Pharmacokinetics of RO7017773 in Healthy Participants

Start date: December 17, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the effect of multiple oral doses of itraconazole on the pharmacokinetics of RO7017773 in healthy volunteers.

NCT ID: NCT03774550 Completed - Atrial Fibrillation Clinical Trials

Atrial Fibrillation Ablation: Radiofrequency or Cryoablation?

ARCFA
Start date: January 25, 2019
Phase:
Study type: Observational

The study aims to compare 3 techniques routinely used for paroxysmal atrial fibrillation ablation: radiofrequency catheter ablation without contact-force, radiofrequency catheter ablation with contact-force and cryoablation. The hypothesis is the non-inferiority between the 3 techniques in terms of free-from atrial fibrillation survival (primary criteria). It will also compare lenght of procedure, radioscopy time and immediate complications (secondary criteria).