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NCT ID: NCT02652559 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Initiation of Long-term Non-invasive Ventilation in COPD

RECONSIDER
Start date: June 2016
Phase: N/A
Study type: Interventional

Rationale: Application of long-term non-invasive ventilation (NIV) in stable chronic obstructive pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure (CHRF) has recently been shown to improve survival and quality of life when applied with sufficiently high inspiratory pressures and adequate backup breathing frequencies (so called high-intensity NIV). However, for a broader implementation of this therapy in a potentially large group of patients, important issues have to be solved. First, the initiation of high-intensity NIV, currently performed in the hospital, is often time-consuming, expensive and inconvenient for patients. Secondly, although clinicians recognise that not all patients benefit, it is not known which factors predict a positive response. Objectives: 1. To investigate whether home initiation of chronic NIV in stable COPD patients with CHRF is non-inferior to inpatient initiation. 2. To investigate predictors of a favourable response to chronic NIV in COPD patients with CHRF. Study design: The study is 1:1 two-arm parallel group randomised controlled trial comparing the usual inpatient NIV initiation to home initiation. Study population: Seventy-two COPD patients with a NIV indication (COPD GOLD stage III or IV; partial arterial carbon dioxide pressure (PaCO2) > 6.0 kPa in stable condition, i.e. no COPD exacerbation for 4 weeks and a pH > 7.35), a sufficient social network at home, without severe cardiac comorbidities, will be included. Intervention: Home initiation of NIV will be compared with standard in-hospital initiation. NIV at home will be titrated by a specialised nurse of our home mechanical ventilation centre (HMV) on transcutaneously measured gas exchange and respiratory electromyography and will be adjusted with the use of telemedicine. Main study parameters/endpoints: 1. To investigate non-inferiority of home initiation, the change in arterial carbon dioxide pressure after 3 months treatment will be the primary outcome. Secondary outcomes are safety, change in lung function, health-related quality of life (HRQoL) and costs. 2. To investigate predictors of a favourable response, patient demographics, and baseline data on lung function as well as measures of respiratory muscle activity, arterial blood gases, comorbidities, inflammatory blood markers and anxiety and depressions scores will be collected of all patients.

NCT ID: NCT02652494 Completed - Psoriasis Clinical Trials

Observational Study of Apremilast in Patients With Psoriasis in The Netherlands

APRIL
Start date: February 22, 2016
Phase:
Study type: Observational

This is a multicenter, prospective, non-interventional, observational single arm study. Two-hundred patients will be recruited in the Netherlands over a one year period. In all cases, the decision to treat the patient with apremilast will be made prior to the decision to enter the subject into this study. Treatment will be according to routine clinical practice and based on recommendations as per the SPC of apremilast (Otezla®). Recruitment will continue until 200 patients have entered the study. Each patient will be followed for 12 months.

NCT ID: NCT02651987 Completed - Clinical trials for Midgut Neuroendocrine Tumours

Efficacy and Safety Study in Pancreatic or Midgut Neuroendocrine Tumours Having Progressed Radiologically While Previously Treated With Lanreotide Autogel® 120 mg

CLARINET FORTE
Start date: December 15, 2015
Phase: Phase 2
Study type: Interventional

This study aims to explore the efficacy and safety of lanreotide Autogel® 120 mg administered every 14 days in subjects with grade 1 or 2, metastatic or locally advanced, unresectable pancreatic or intestinal neuroendocrine tumours (NETs) once they have progressed on the standard dose of lanreotide Autogel® 120 mg every 28 days.

NCT ID: NCT02651779 Completed - Clinical trials for Displaced Complete Articular Distal Radius Fractures

Internal Plate Fixation vs. Plaster in Complete Articular Distal Radial Fractures

VIPAR
Start date: June 19, 2015
Phase: N/A
Study type: Interventional

There is no consensus about the best treatment for patients with displaced complete articular distal radius fractures (AO type C fractures). Despite this lack of consensus and the lack of available literature on comparative data to guide treatment for this patient population, operative treatment with plate fixation has gained popularity. The aim of this study is to compare the functional outcome of open reduction and plate fixation with closed reduction and plaster immobilisation in adult patients (18-75 years) with displaced complete articular distal radius fractures.

NCT ID: NCT02651675 Terminated - Clinical trials for Homozygous Familial Hypercholesterolemia (HoFH)

A Gene Therapy Study for Homozygous Familial Hypercholesterolemia (HoFH)

Start date: March 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This first-in-human study is intended to evaluate the safety and preliminary effectiveness of AAV (Adeno-associated virus)-based liver-directed gene therapy in the treatment of adults with Homozygous Familial Hypercholesterolemia (HoFH).

NCT ID: NCT02650817 Completed - Clinical trials for Metastatic Breast Cancer

Phase IB Study to Evaluate RAD1901 on the Availability of Estrogen Receptor Binding Sites in Metastatic Breast Cancer

Start date: April 1, 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to visualize and quantify ER-binding sites during treatment with Elacestrant (RAD1901)

NCT ID: NCT02650713 Completed - Solid Tumors Clinical Trials

A Study of the Safety, Pharmacokinetics, and Therapeutic Activity of RO6958688 in Combination With Atezolizumab in Participants With Locally Advanced and/or Metastatic Carcinoembryonic Antigen (CEA)-Positive Solid Tumors

Start date: January 7, 2016
Phase: Phase 1
Study type: Interventional

This is an open-label, multicenter, dose-escalation and expansion Phase Ib clinical study of RO6958688 in combination with atezolizumab. Part I of the study is subdivided into parts IA and IB. Part IA is dose escalation with a starting dose of 5 mg of RO6958688 given QW (once a week) and a fixed, flat dose of 1200 mg given Q3W (every 3 weeks) of atezolizumab, to evaluate the safety and determine the MTD of RO6958688 in combination with atezolizumab. Part IB is a dose/schedule finding part that will explore different administration schedules of RO6958688 in combination with atezolizumab (1200 mg Q3W) to establish the appropriate dose/schedule of RO6958688 in combination with atezolizumab.

NCT ID: NCT02650479 Completed - Clinical trials for Healthy Adult Male and Female Volunteers

Study of the Effects of Intravenous Exenatide on Cardiac Repolarization

Start date: January 2016
Phase: Phase 1
Study type: Interventional

Two-Part, Randomized, Placebo and Active-Controlled, Double-Blind, Thorough QT Study Evaluating the Effects of Intravenous Exenatide on Cardiac Repolarization in Healthy Male and Female Volunteers

NCT ID: NCT02650453 Recruiting - Venous Thrombosis Clinical Trials

Ongoing Registry of Deep Venous Reconstructions

Start date: September 2009
Phase: N/A
Study type: Observational

Ongoing registration of deep venous obstructive disease patients treated by means of percutaneous transluminal angioplasty (PTA) and stenting with or without endophlebectomy (surgical desobstruction, also termed endovenectomy) of the common femoral vein and/or arteriovenous fistula creation.

NCT ID: NCT02650128 Completed - Clinical trials for Coronary Artery Disease

Shockwave Coronary Rx Lithoplasty® Study (Disrupt CAD I)

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

Prospective, multi-center, single arm study designed to evaluate the safety and performance of the Shockwave Coronary Rx Lithoplasty® System to treat calcified lesions in the coronary arteries for the purpose of enhancing the placement of stents and reducing the ultimate residual stenosis. Patients will be followed through discharge and at 30 and 180 days.