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NCT ID: NCT02008305 Terminated - Clinical trials for Occlusion or Malformation of a Cerebral Vessel

Comparison of Two Protocols of Optimization of X Ray Radiations in Pediatric Interventional Neuroradiology

MINIRAD
Start date: November 2013
Phase: N/A
Study type: Interventional

Interventional Neuroradiology replaces surgery. This technology requires various exposition to X rays : number of X rays photographs, radioscopy, distance between patient and detector, speed of acquisition of X-rays photographs, high tension and intensity. The manipulator must find the right balance between quality of photographs and dose delivered to the patient (optimization). Children are particularly exposed to these risks of irradiation (sensitivity to X-rays and long life expectancy with risks. So, it is fundamental to optimize the dose delivered during the procedures. The investigators propose to analyse a study comparing two protocols of optimization of doses. The investigators' hypothesis is that the protocol experimented in this trial allows less radiation of the children, compared to the usual protocol.

NCT ID: NCT02005133 Terminated - Clinical trials for Wet Age-related Macular Degeneration

A Prospective, Observational, Multicentre, 2 Year Study Evaluating the Use of Eylea (Aflibercept) for the Treatment of Neovascular (Wet) Age-related Macular Degeneration in UK NHS Opthalmology Clinics

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

To assess the use of aflibercept over a 2 year period in VEGF inhibitor naive and prior treated wet AMD patients managed in 'real wold' clinic settings.

NCT ID: NCT02003326 Terminated - Clinical trials for Acute Respiratory Distress Syndrome

Strain and Blood Inflammatory Markers as Prognostic Tools for ARDS AMIS (ARDS - Markers of Inflammation - Strain)

AMIS
Start date: November 2013
Phase: N/A
Study type: Interventional

The objective is determine the strain measured at the bedside could be a dynamic prognostic marker of during Acute respiratory Distress Syndrome (ARDS).

NCT ID: NCT02002689 Terminated - Clinical trials for PTCH1 or SMO Activated Solid and Hematologic Tumors

LDE225 for Patients With PTCH1 or SMO Mutated Tumors

SIGNATURE
Start date: February 2014
Phase: Phase 2
Study type: Interventional

The purpose of this signal seeking study is to determine whether treatment with LDE225 demonstrates sufficient efficacy in hedgehog pathway-mutated solid tumors and/or hematologic malignancies to warrant further study

NCT ID: NCT02000375 Terminated - Clinical trials for Estrogen Receptor Positive Breast Cancer

A Phase II Study Evaluating the Role of Androgen Receptors as Targets for Therapy of Pre-treated Post-menopausal Patients With ER/PgR-negative/AR-positive or ER and/or PgRpositive/ AR-positive Metastatic Breast Cancer (ARTT)

ARTT
Start date: March 2013
Phase: Phase 2
Study type: Interventional

A phase II non randomized study evaluating the role of Androgen Receptors as Targets for therapy of pre-treated postmenopausal patients with ER/PgR-negative/AR-positive or ER and/or PgR-positive/AR-positive metastatic breast cancer. Study Design: Multicentric, Open-label not randomized trial. Description of Study Treatment: Daily oral administration of DHEA (Dehydroepiandrosterone) at the dosage of 100 mg/die in combination with a daily oral administration of anastrozole at dosage of 1 mg/die or letrozole at the dosage of 2.5 mg/die or exemestane at the dosage of 25 mg/die without interruption until discontinuation for progression of disease, unacceptable toxicity or discontinuation/withdrawal of participants from study treatment. Number of Subjects: 12 patients per group in the first step; if the number of responders is greater or equal to 2, recruitment will continue up to a total of 35 patients (per group). For the biological part, we will evaluate: 1. Correlation between AR expression and clinical and biological features (tumor size, nodal status, histotype, grading, proliferative index, ER, PgR, HER2) 2. Evaluation of AR expression on primitive and/or metastatic site in the two distinct populations of patients: ER/PgR- negative/ARpositive and ER-positive and/or PgR-positive/AR-positive 3. Evaluation of ER, PgR, HER2 expression on tumor cells of metastatic site (when it is possible) and comparison with the same features of primitive tumor. 4. CTCs analysis in term of molecular characteristics (gene expression and mutations) and functionality (vitality and tumorigenicity). 5. Prognostic and predictive role of Circulating Tumor Cells (CTC) evaluated at baseline before study treatment and at the moment of discontinuation of treatment.

NCT ID: NCT02000037 Terminated - Clinical trials for Assess the Effect of an IR Reflexotherapy on Overweight and Class I Obese People

Interest in the Medium Term of an Infrared Reflexotherapy on Overweight or Class I Obese People

REFLEX-IR
Start date: October 18, 2013
Phase: N/A
Study type: Interventional

The study aim is to Assess the Effect of an IR Reflexotherapy on Overweight and Class I Obese People.

NCT ID: NCT01999855 Terminated - Clinical trials for Asthmatic Patients and Control Group

Frequency of Dysphonia in Asthmatic Patients

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

For many years, it is known that asthmatics have more often dysphonia. However, no study has so far analyzed the reality of dysphonia in asthmatic by making phoniatric tests. The etiology of dysphonia in asthmatic remains controversial. Indeed, for a long time, inhaled corticosteroids have been considered as responsible for organic abnormalities of the vocal cords. We hypothesized that women with asthma have more often dysphonia, and that dysphonia is rather functional origin.

NCT ID: NCT01999660 Terminated - Clinical trials for Prostate Cancer Patients Treated by Radiotherapy

Post-marketing Surveillance Regarding Efficacy and Safety of SpaceOARâ„¢

Start date: November 2013
Phase:
Study type: Observational

A treatment with SpaceOARâ„¢ hydrogel does reduce late toxicity Grad 2 and Grad 3 of radiation therapy in prostate cancer patients

NCT ID: NCT01998399 Terminated - Clinical trials for Community Acquired Pneumonia, Severe

Ticagrelor in Severe Community Acquired Pneumonia

TCAP
Start date: August 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the drug ticagrelor will be an effective treatment for patients with severe community acquired pneumonia. The primary objective is to reduce all-cause mortality in the ticagrelor group compared to the placebo group.

NCT ID: NCT01996852 Terminated - Prostate Cancer Clinical Trials

Improving Erectile Function and Quality of Life After Prostate Cancer Treatment

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

This is a research study of erectile dysfunction (ED) in men diagnosed with prostate cancer. 144 patients and partners will participate in the study. The purpose of this study is to test a new treatment that combines a cognitive-behavioral intervention with medication and a vacuum constrictive device to treat ED. This new treatment consists of multiple therapeutic elements that enhance compliance with medical treatment and increase sexual activity through enhancement of the sensual pleasure of sex and partner support.