Many Locations, France
Impact of an Early and Extended Rehabilitation Program Combining Individually Tailored Nutrition and Physical Activities on Patient Outcomes After Invasive Mechanical Ventilation and Vasopressor Therapy in the ICU
Phase
N/ASpan
157 weeksSponsor
Nantes University HospitalDieppe
Recruiting
Noninvasive 3D Mapping in Persistent Atrial Fibrillation, to Describe Modifications of the Arrhythmogenic Substrate After Pulmonary Vein Isolation and Identify Potential Predicting Factors of Ablation Success
Phase
N/ASpan
160 weeksSponsor
University Hospital, RouenDieppe
Recruiting
Efficacy of Early Intravenous High-dose Vitamin C in Post-cardiac Arrest Shock.
Phase
2Span
109 weeksSponsor
Centre Hospitalier de BethuneDieppe
Recruiting
Mean Arterial Pressure After Out-of-hospital Cardiac Arrest
Phase
N/ASpan
183 weeksSponsor
Centre Hospitalier le MansDieppe
Recruiting
Post Market Clinical Follow-up Study for Arthroplasty Shoulder System of FX Solutions at the Long Term
Inclusion Criteria - Adult patient (≥ 18 years old) who received one of FX Solutions Shoulder System for indication of hemi or total shoulder replacement. - Patient implanted between 2011 and 2015 with a minimum follow-up of 7 years - Patient has been informed of his participation in a clinical study and did not object to data collection - Patient insured with a social security system Exclusion Criteria - Patient who does not meet the inclusion criteria above - Protected adult - People deprived of their liberty Study Objectives - Primary Objective: To assess functional improvement according to the Constant score evolution compared to its preoperative value - Secondary Objectives, assessment of: To assess against the preoperative value: - the Subjective Shoulder Value score evolution - the American Shoulder and Elbow Surgeons shoulder score evolution To describe in real life - The complications rate - The long-term range of motion - The revision rates and the prosthesis survival curve Endpoints - Primary Endpoint will be the current Constant score (measured during the assessment). The functional improvement will be evaluated according to the evolution of this score compared to its preoperative value. - Secondary Endpoints: Current ASES and SSV scores Current range of Motion Revision rate at a long-term follow-up. Calculation of the survival rates The incidence of complications occurring since implantation Revision rates and survival rates of prostheses Study Groups Group 1: Subjects implanted with HUMELOCK I & II® Anatomic Shoulder System 2011 to 2013 Group 2: Subjects implanted with HUMELOCK II® Reversible System 2011 to 2013 Group 3: Subjects implanted with HUMELOCK Reversed® Shoulder System - 2012 - 2013 Group 4: Subjects implanted with EASYTECH® Anatomic Shoulder System - 2013 - 2014 Group 5: Subjects implanted with EASYTECH® Reversed Shoulder System (For Primary intention only) - 2013- 2014 Group 6: additional group for Subjects who were implanted with EASYTECH® Reversible Shoulder System (Exclusively for Revision of Easytech Anatomic) - 2013 -2014, if applicable Group 7: Subjects implanted with HUMERIS® Anatomic Shoulder System 2014 to 2015 Group 8: Subjects implanted with HUMERIS® Reversible Shoulder System 2014 to 2015
Phase
N/ASpan
30 weeksSponsor
FX SolutionsDieppe
Recruiting
Simulation-based Training for Nurses and Arteriovenous Fistula Puncture in Chronic Hemodialysis Patients
Currently, the technique of arteriovenous fistula puncture is transmitted by companionship within hemodialysis units. Although the main principles of the technique are well known and common to all hemodialysis units, strong rationales are still lacking to standardize fine practices such as the relative position of the needles, the angle of attack of the needle at puncture, the position of the bevel at the time of puncture and once the needle is in the vascular lumen. The training of professionals using a simulation-based training program on the approach to arteriovenous fistula puncture, in a process of optimizing practices and continuous improvement of care, while respecting the principles of andragogy, seems to be a suitable tool. This program is built in a multi-professional team from nephrology, nursing and health simulation. The aim of this study is to evaluate whether a simulation-based training program for nurses, concerning arteriovenous fistula puncture puncture, would allow to decrease the adverse events related to punctures. The investigators propose a prospective, comparative, randomized, multicenter study involving 8 hemodialysis centers. The primary objective is to compare the number of arteriovenous fistula puncture-related adverse events between: - A group receiving theoretical training + simulation-based training (4 centers) - A group receiving theoretical training only (4 centers) Will be included all adult patients who are to receive an arteriovenous fistula puncture puncture by a hemodialysis-trained IDE, during a scheduled chronic dialysis session. This study is innovative for several reasons: - simulation-based training in continuing education, among professionals is not widely used - simulation-based training in continuing education allows the conceptualization of the team approach to VF by its modeling in simulation - the evaluation of the direct benefit of the training on the patient, a Kirkpatrick level 4, is very little described in the literature. Thus, this study is of major interest to patients managed in nephrology with the simulation-based training tool.
Phase
N/ASpan
108 weeksSponsor
University Hospital, CaenDieppe
Recruiting
Role of PET Scan in the Evaluation of Early Response to Maintenance Treatment in Advanced Non-small-cell Lung Cancer
The purpose of the study is to optimize survival by an adapted metabolic imaging therapy in patients with advances non-small cell lung cancer. The primary objective of the study is to evaluate the role of SUV and metabolic volume measured by FDG PETScan in the early prediction of treatment response. 80 patients will be included in 2 years. They will be follow up for one year for monitoring the progression free survival.
Phase
2Span
278 weeksSponsor
Centre Henri BecquerelDieppe
Recruiting
Home Non Invasive Ventilation for COPD Patients
Phase
N/ASpan
735 weeksSponsor
University Hospital, RouenDieppe
Recruiting
Effectiveness of a Patient Therapeutic Education Program in Improving Pain Management
Phase
N/ASpan
315 weeksSponsor
Centre Francois BaclesseDieppe
Recruiting
Status Epilepticus in the Critically Ill Patients
Phase
N/ASpan
566 weeksSponsor
Ictal GroupDieppe
Recruiting
Healthy Volunteers