CenterWatch
  • Search Clinical Trials
  • Clinical Trial Listings
  • Volunteer
  • Learn About Clinical Trials

Cherbourg-en-côte, France

< 2 Miles
Filters

Type

Distance
Age
0
0
Gender
Trial Phase
Sponsor
  • Research of the Consequences on the Digestive Tract Following the Proposed Treatments for a Urinary Infection in Children

    Phase

    N/A

    Span

    315 weeks

    Sponsor

    Centre Hospitalier Intercommunal Creteil

    Nogent-sur-Marne

    Recruiting

  • (DIS)AGreement of Relatives Regarding Ethical End-of-life Decisions in ICU.

    Context In the ICU, the vast majority of patients die following a life-sustaining therapies (LST) limitation decision. Most often, the patient is not able to express himself and has not made his wishes known beforehand, for example in the form of advance directives. The "relatives" are then the only recourse to state the patient's wishes, without any guarantee that they are aware of them. In France, the final decision is made by the physician (or the medical team) who is responsible for it. In this context, disagreements and even real legal conflicts on LST limitation decisions between relatives and physicians seem to be more and more frequent. To our knowledge, few data exist on the frequency of these disagreements over LST limitation decisions. Purpose The main objective of this study is to evaluate the frequency of disagreements between relatives and physicians over LST limitation decisions in adult intensive care. The secondary objectives are: - To assess the level of agreement/disagreement between family members and physicians regarding LST limitation decisions - To assess the proportion of disagreements experienced as conflictual - To assess the impact of the disagreement on the LST limitation decision (implementation of the decision, time between the decision and its implementation, length of hospitalization...) - To describe possible factors that contribute to disagreement and conflict - To describe national LST limitation decision-making practices.

    Phase

    N/A

    Span

    89 weeks

    Sponsor

    Société Française d'Anesthésie et de Réanimation

    Bry-sur-Marne

    Recruiting

  • Detection of Amyloid Deposits in the Wrist by MRI With Mapping and High Resolution Sequences in Systemic Amyloidosis (AMYLOCARP)

    Phase

    N/A

    Span

    118 weeks

    Sponsor

    Ramsay Générale de Santé

    Champigny-sur-Marne

    Recruiting

    Healthy Volunteers

  • Chemotherapy and Immunotherapy as Treatment for MSS Metastatic Colorectal Cancer With High Immune Infiltrate

    Phase

    2

    Span

    182 weeks

    Sponsor

    Federation Francophone de Cancerologie Digestive

    Champigny-sur-Marne

    Recruiting

  • Effectiveness of a Patient Therapeutic Education Program in Improving Pain Management

    Phase

    N/A

    Span

    315 weeks

    Sponsor

    Centre Francois Baclesse

    Champigny-sur-Marne

    Recruiting

  • Evaluating the Benefit of Hypnoanalgesia Versus Neuroleptanalgesia During Hand Surgery

    In a population of patients undergoing hand surgery and divided into two groups according to the anesthesia protocol administered in addition to locoregional anesthesia by truncal block: Group 1: neuroleptanalgesia Group 2: hypnoanalgesia Primary objective The main objective of the study is to compare changes in preoperative anxiety between the two groups, between two measurements taken preoperatively (before anxiety management) and at the end of surgery. This level will be evaluated using a VAS rated from 0 to 10. Secondary objectives Comparing groups: - Intraoperative pain - Total duration of surgical procedure, ICU stay and hospitalization - Amount of additional sedative treatment administered during surgery - Post-operative pain - Patient satisfaction - Intraoperative and immediate postoperative adverse events

    Phase

    N/A

    Span

    55 weeks

    Sponsor

    GCS Ramsay Santé pour l'Enseignement et la Recherche

    Champigny-sur-Marne

    Recruiting

  • Measurement of the Clinical and Radiological Performance Impact of the Root Canal Treatment With BioRootTM RCS.

    Phase

    N/A

    Span

    385 weeks

    Sponsor

    Septodont

    Villiers-sur-Marne

    Recruiting

  • Diagnostic Accuracy of Rapid Molecular Tests for Group A Streptococcal Pharyngitis Using Saliva Samples

    Group A streptococcus (GAS) is found in 20% to 40% of cases of childhood pharyngitis; the remaining cases are viral. Streptococcal pharyngitis ('strep throat') deserves antibiotics, while these are not indicated in viral cases. Because signs and symptoms of streptococcal and viral cases overlap, most guidelines recommend relying on a diagnostic test to identify Group A streptococcus to select who should receive antibiotics. In most settings, the first-line test to detect Group A Streptococcus is a rapid antigen detection test based on a throat swab, and the reference standard to identify streptococcal cases is throat culture. Recently, new rapid tests were developed. They use molecular techniques, such as rapid PCRs or LAMP, based on throat swabs. We hypothesize that these new molecular tests are sensitive enough to be performed on saliva swabs instead of throat swabs. Collecting saliva is less invasive and could be done by personnel with limited training.

    Phase

    N/A

    Span

    109 weeks

    Sponsor

    Centre Hospitalier Intercommunal Creteil

    Nogent-sur-Marne

    Recruiting

  • ECT in Ultra-resistant Schizophrenia

    Phase

    N/A

    Span

    274 weeks

    Sponsor

    Centre Hospitalier du Rouvray

    Neuilly-sur-Marne

    Recruiting

  • Assessment of Pain During Intramuscular Injection Delay in Adult Psychiatry

    Phase

    N/A

    Span

    206 weeks

    Sponsor

    Centre hospitalier de Ville-Evrard, France

    Neuilly-sur-Marne

    Recruiting

1-10 of 20
CenterWatch

5000 Centregreen Way, Suite 200
Cary, NC, 27513, USA

Phone: 703.538.7600
Toll Free: 888.838.5578

  • Disclaimer
  • Privacy Policy
  • Term of Use
  • Do Not Sell My Personal Information