Mount Stewart, Canada
Prevention of Postpartum Venous Thromboembolism in Women at Intermediate Risk
Phase
4Span
170 weeksSponsor
University Hospital, BrestBrest
Recruiting
Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib
Phase
3Span
157 weeksSponsor
Incyte CorporationBrest
Recruiting
Characterization of "Bamboo" and Other Vocal Cord Lesions Responsible for Dysphonia in Patients With Systemic Autoimmune Diseases (BAMBOO)
Patients with a systemic autoimmune disease may face to the occurrence of a dysphonia during the course of their disease. Specific etiologies must be sought for, such as "bamboo nodes", previously reported on small series, especially in patients with systemic erythematosus lupus, but also in other connective tissue disease such as Sharp syndrome, primary Sjögren disease and anti-synthetase syndrome. These nodes are made of fibrosis and immune complexes have been described. The treatment relies on vocal reeducation, oral steroids and sometimes surgery. Other irritative factors must be avoided such as stopping tobacco or treating a gastroesophageal reflux. Increasing the immunosuppressive regimen of the autoimmune disease has also been suggested, but the management is not codified due to the rarity of this condition. Rheumatoid nodules of the vocal cords have also been described in rheumatoid arthritis as well as cricoarytenoid joint arthritis. Granuloma of the vocal cords have also been reported in granulomatosis with polyangiitis. Other non specific etiologies should also be sought for such as mucosal ulcerations, submucous edema or hematoma, or vocal cord palsy. Owing to the rare series of dysphonia reported in a context of systemic auto-immunity, the aim of this retrospective study is to provide an inventory of the specific and non specific lesions that can cause dysphonia in patients with systemic autoimmune diseases, with the assessment of potential diagnosis delays and therapeutics. Main objective : To characterize the cord vocal lesions responsible for dysphonia in patients with systemic autoimmune diseases. Secondary objectives : - To assess the proportion of "bamboo nodes" compared to non specific lesions in patients with a systemic autoimmune disease suffering from dysphonia. - To identify potential diagnosis delays. - To describe the management of these lesions. - To identify risk factors associated with these lesions.
Phase
N/ASpan
26 weeksSponsor
University Hospital, BrestBrest
Recruiting
Hepatic Doppler to Assess Venous Congestion During Invasive Mechanical Ventilation (DOHECOV)
Phase
N/ASpan
189 weeksSponsor
University Hospital, BrestBrest
Recruiting
Perioperative Dynamics of Energy Expenditure in Oesophagectomy Patients
The results of this study should enable current nutrition protocols to evolve and nutritional support to be incorporated into a more global project of individualised perioperative medicine.
Phase
N/ASpan
174 weeksSponsor
University Hospital, RouenBrest
Recruiting
Epidemiology of Gonococcal Arthritis (EpGAr)
Phase
N/ASpan
22 weeksSponsor
University Hospital, BrestBrest
Recruiting
Epidemiological Study of a Prospective Cohort of Patients Aged 60 and Over Managed for Acute Myeloid Leukemia (AML) and Receiving Intensive Induction Therapy
Phase
N/ASpan
835 weeksSponsor
French Innovative Leukemia OrganisationBrest
Recruiting
Children, Adolescents and Young Adults with Myeloproliferative Neoplasia: Study of Clinico-biological Characteristics and Complications (VYP)
Phase
N/ASpan
783 weeksSponsor
University Hospital, BrestBrest
Recruiting
A MULTICENTER, SEEKING SIGNAL, RANDOMISED, OPEN-LABEL PHASE II OF RELATLIMAB AND NIVOLUMAB VS NIVOLUMAB ALONE IN LOCALLY ADVANCED CERVICAL CANCERS
Primary Objective * To evaluate the clinical activity of relatlimab and nivolumab induction treatment before standard CCRT in locally advanced cervical cancer Secondary Objectives - To further document the clinical activity of relatlimab and nivolumab - To document the safety of the proposed combination in the target population Exploratory Objectives - To identify candidate biomarkers that may correlate with likelihood of clinical benefit/response using serial blood and tumor sample collection. - To explore the factors (including biomarkers) that may influence response (where response is defined broadly to comprise efficacy, tolerability or safety) or to explore mechanisms of resistance to study treatment.
Phase
2Span
316 weeksSponsor
ARCAGY/ GINECO GROUPBrest
Recruiting