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NCT ID: NCT04554927 Recruiting - Breast Cancer Clinical Trials

Impact of Web Application Support Versus Standard Management on Compliance With Adjuvant Hormone Therapy at 18 Months in Patients Treated for Breast Cancer

WEBAPPAC
Start date: September 3, 2020
Phase: N/A
Study type: Interventional

The investigators hypothesize that the implementation of a Web-application in patients initiating adjuvant hormone therapy for breast cancer brings a benefit on treatment adherence and quality of life.

NCT ID: NCT04554914 Recruiting - Clinical trials for Stem Cell Transplant Complications

A Study to Evaluate Tabelecleucel in Participants With Epstein-barr Virus-associated Diseases

Start date: July 14, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of tabelecleucel in participants with Epstein-Barr virus (EBV) associated diseases.

NCT ID: NCT04554849 Active, not recruiting - Gender Dysphoria Clinical Trials

Demographic Characteristics and Psychosocial Health of Transgender People

DyGeDem
Start date: July 24, 2020
Phase:
Study type: Observational

To study demographic characteristics of subjects referred to endocrine care for gender dysphoria and their psychosocial health

NCT ID: NCT04554602 Active, not recruiting - Endometriosis Clinical Trials

Fusion Ultrasound for Diagnosis and Monitoring of Endometriosis Lesions

ENDOFUSION
Start date: March 1, 2021
Phase:
Study type: Observational

The aim of the study is evaluate the fusion ultrasound performance compared to MRI and coelioscopy diagnosis when a surgical intervention is performed.

NCT ID: NCT04554290 Completed - Clinical trials for Giant Cell Arteritis

Giant Cell Arteritis and Differential Diagnoses Associated With Positive Temporal Artery Biopsy

Start date: August 1, 2020
Phase:
Study type: Observational

Temporal artery biopsy is a useful tool helping to the diagnosis of giant cell arteritis. However, other diagnoses might be associated with abnormal temporal artery biopsy. The purpose of this study is to describe the frequency of giant cell arteritis differential diagnoses with positive temporal artery biopsy.

NCT ID: NCT04554277 Recruiting - Heart Failure Clinical Trials

Medico-economic Evaluation of Therapeutic Adaptation Guided by the Soluble Suppression of Tumorigenicity 2 (sST-2) Biomarker in the Management of Patients With Acute Heart Failure

ICAME
Start date: April 27, 2021
Phase: N/A
Study type: Interventional

Management of patients with heart Failure remains a major health concern because of the high rate of rehospitalization, mortality and induced-cost. Biomarkers could help to guide the management of patients with heart failure (HF). Soluble suppression of tumorigenicity 2 (sST2) appears as a promising biomarker. As a working hypothesis, we postulate that sST2 values monitoring could be an helpful guide for medical management in an attempt to reduce hospital readmission.

NCT ID: NCT04554264 Withdrawn - Covid19 Clinical Trials

Complicated Grief in ICU in the Aftermath of COVID-19

DEPARTS
Start date: September 1, 2020
Phase: N/A
Study type: Interventional

An increased proportion of deaths occur in the intensive care unit (ICU). Some amenable factors such as end-of-life practices may contribute to complicated grief. Because of the COVID-19 pandemic, visitor restrictions in health care facilities have been implemented. Families were also unable to implement usual funerals. The investigators hypothesize that these policies and practices may impact grief during covid-19 pandemic. The aim of this study is to evaluate the prevalence of complicated grief after death of a relative in the ICU during the COVID-19 pandemic.

NCT ID: NCT04554173 Completed - Clinical trials for Neurogenic Thoracic Tumors

An Appraisal of Minimal Invasive Surgery for Thoracic Neurogenic Tumour

DIUOP
Start date: April 24, 2020
Phase:
Study type: Observational

Mediastinal neurogenic tumors are relatively rare in children. Surgical resection is essential. Minimal invasive surgery is more and more used in pediatric population, but his evaluation for resection of thoracic neurogenic tumors is little studied. Thoracotomy has specific long terms post operative complications. When compared to thoracotomy, thoracoscopy shows less operative blood loss, shorter duration of chest tube ans length of stay. Recently, the indications of thoracoscopic approach have been assessed according to the presence or absence of image-defined risk factors (IDRF) at diagnosis and after preoperative chemotherapy in a monocentric retrospective study. The investigators aimed to conduct a multicentric retrospective study to assess the role of thoracoscopy in neurogenic thoracic tumours according to the presence or absence of IDRF at diagnosis, the surgical complications and outcome.

NCT ID: NCT04554108 Recruiting - Osteomyelitis Clinical Trials

Acute Non-severe Osteomyelitis in Children - Outpatient Management Strategy With Oral Antibiotic Therapy Compared to a Standard Strategy With Conventional Hospitalization and Intravenous Antibiotic Therapy: a Randomized Open-label Non-inferiority Study With Bayesian and Medical-economic Analyses.

POOMA
Start date: May 31, 2021
Phase: N/A
Study type: Interventional

The incidence of bone and joint infections (BJI) in children (osteomyelitis, septic arthritis and spondylodiscitis) is 22 per 100,000 children in France. Every year, 3,000 children are hospitalized for BJI, 46% of whom are hospitalized for osteomyelitis. The clinical pictures of BJI are varied: some are severe from the outset; others are non-severe, such as BJIs in Kingella kingae, which are most common in children between the ages of 6 months and 5 years. Currently, the management of children's BJI, regardless of their severity, involves initial hospitalization to start intravenous antibiotic therapy. This non-inferiority trial evaluates, in children with acute osteomyelitis with no severity criteria, less invasive outpatient management with an oral antibiotic treatment given at the outset compared to standard management. Main objective : Demonstrate the non-inferiority of an ambulatory management strategy versus a standard strategy involving hospitalization on complete recovery without relapse at 6 months after an episode of acute osteomyelitis in children aged 1-4 years without severity criteria. Primary endpoint: Complete cure without relapse at 6 months defined by the absence of clinical signs of osteomyelitis at 6 months AND the absence of secondary septic complications (septic arthritis, periosteal abscess) before the end of antibiotic therapy AND the absence of relapse or rehospitalization for osteomyelitis related to the initial infection. This criterion will be assessed blindly by an adjudication committee. Randomized controlled trial of non inferiority, with active control, in open multi-center. The control or experimental arm allocation (1:1 ratio) will be open-label of the physician, patient and parents. This is a PROBE study: The evaluation of the main judgment criterion will be carried out blindly by an adjudication committee.

NCT ID: NCT04553692 Recruiting - Colorectal Cancer Clinical Trials

Phase 1a/1b Study of Aplitabart (IGM-8444) Alone or in Combination in Participants With Relapsed, Refractory, or Newly Diagnosed Cancers

Start date: September 23, 2020
Phase: Phase 1
Study type: Interventional

This study is a first-in-human, Phase 1a/1b, multicenter, open-label study to determine the safety, tolerability, and pharmacokinetics of aplitabart as a single agent and in combination in participants with relapsed and/or refractory solid or hematologic cancers, as well as newly diagnosed cancers, and an open-label, randomized study of aplitabart+FOLFIRI+bevacizumab.