25 results match your criteria: "Soladis Clinical Studies[Affiliation]"
Medicine (Baltimore)
December 2024
Physiotherapy Clinic, Antibes, France.
The first-line treatment for nonspecific low back pain (LBP) relief is physical exercise; however, there is no uniformity in recommendations regarding the type of exercise, and physicians predominantly prescribe pharmacological treatments. This creates a treatment gap in non-pharmacological management of LBP. Preliminary data suggest that manual therapy and acupressure could be relevant therapeutic options.
View Article and Find Full Text PDFInt Angiol
December 2023
Vascular Screening and Diagnostic Center, University of Nicosia Medical School, Nicosia, Cyprus -
Introduction: The prevalence of lower limb edema is high among patients with chronic venous disease (CVD). Several clinical studies with various designs have assessed the effect of micronized purified flavonoid fraction (MPFF) on edema. The aim of this work was to provide a comprehensive and accurate evaluation of the reduction in ankle and calf circumference as an indicator of lower limb edema reduction in patients with CVD treated with MPFF by combining studies that use different designs in a single group meta-analysis.
View Article and Find Full Text PDFJ Clin Pharmacol
November 2023
Octapharma France SAS, Boulogne-Billancourt, France.
Human fibrinogen concentrate (Fibryga) received temporary approval for fibrinogen replacement therapy in France (2017), with subsequent full approval for congenital and acquired hypofibrinogenemia. We evaluated real-world use for on-demand treatment of bleeding and prophylaxis to enhance our knowledge on fibrinogen concentrate as an option for fibrinogen replacement. Data were retrospectively collected from adult and pediatric patients with fibrinogen deficiency.
View Article and Find Full Text PDFAllergy Asthma Proc
September 2022
Department of Internal Medicine and Clinical Immunology, Lille University, Inserm, Lille University Hospital, CREAK, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, France.
Acta Paediatr
February 2022
Pediatric nutrition and gastroenterology department, Trousseau hospital, APHP, Paris, France.
Aim: To assess the impact of complementary feeding bottles given at maternity hospital and/or over the first month after discharge from the maternity ward on cow's milk allergy (CMA) risk in breastfed infants.
Methods: Case-control study involving infants aged 6-9 months and who were breastfed for at least 1 month.
Results: In 554 cases with a diagnosis of CMA and 211 controls, feeding bottles at maternity hospital, feeding bottles during the first month of life, avoidance of dairy products during pregnancy or breastfeeding, family history of allergy, intake of antibiotics and consumption of proton-pump inhibitors or antacids by the infant during the first month of life were associated with increased risk of CMA in a univariate model.
Joint Bone Spine
March 2022
Agence Sanitaire et Sociale, Nouméa, New Caledonia.
Objectives: New Caledonia is a Pacific island of 270,000 inhabitants with mixed ethnicities, including Polynesians (10.2%), people from European ancestry (27.2%), and Melanesians (39.
View Article and Find Full Text PDFClin Transl Allergy
August 2021
ALYATEC Environmental Exposure Chamber Strasbourg France.
Background: Environmental exposure chambers (EECs) have been used extensively to study allergic rhinoconjunctivitis. Few studies have been published using EECs in conjunctivitis only, and none have used conjunctival allergen challenge as a selection criterion. The present study validated ALYATEC EEC in allergic conjunctivitis to birch pollen.
View Article and Find Full Text PDFPatient Prefer Adherence
April 2021
University of Lille, Rheumatology Department, Hôpital Roger Salengro, Lille, France.
Purpose: The purpose of the APRIM study (for Adherence Polyarthrite Rhumatoïde Injection Methotrexate) was to investigate the change in treatment adherence of patients with rheumatic arthritis (RA) who switched from oral to subcutaneous methotrexate (MTX).
Patients And Methods: Prospective, observational study in RA patients treated with MTX and switching from oral to subcutaneous (SC) route in real-life conditions. Data on motivations for switch, disease activity (DAS28-CRP), quality of life (AISM-2 SF), disability (HAQ-DI), and adherence to MTX were collected at inclusion (M0) and 6 months later (M6).
Rev Mal Respir
December 2020
Service de pneumologie, hôpital Cochin, AP-HP, université de Paris, institut Cochin (UMR 1016), 75014 Paris, France.
The Pneumo-Quest self-questionnaire was developed to standardize the practice of recollection when welcoming a new patient. It consists of 82 main questions and 34 subsidiary questions to be completed at home by the patients before their first visit to a pulmonologist. This evaluation was carried out on the basis of 137 returned questionnaires.
View Article and Find Full Text PDFJoint Bone Spine
December 2020
Département de Médecine Interne et Immunologie Clinique, CHU Lille, Referral center for rare systemic autoimmune diseases North and Northwest of France, University Lille, Inserm U995 - LIRIC - Lille Inflammation Research International Center, 59000 Lille, France.
Objectives: Hydroxychloroquine (HCQ) is an anchor drug in the treatment of systemic lupus erythematosus (SLE). Adherence to HCQ is key for efficacy. Inaccurate evaluation of adherence could lead to non-justified switch to more expensive or less tolerated drugs.
View Article and Find Full Text PDFEur Respir J
September 2020
APHP, National Reference Centre for Pulmonary Hypertension, Dept of Respiratory and Intensive Care Medicine, Bicêtre Hospital, University Paris-Sud - University Paris Saclay, INSERM UMR_S999, Le Kremlin-Bicêtre, France.
https://bit.ly/3aWZagH
View Article and Find Full Text PDFMedicine (Baltimore)
February 2020
University Paris-Diderot, Patient-Centered Outcomes Research, Paris.
Clin Exp Rheumatol
September 2020
Soladis Clinical Studies, Roubaix, France.
Objectives: Systemic lupus erythematosus (SLE) is a chronic autoimmune multi-organ disease with an unpredictable course. SLE causes functional disability, changes in body appearance, and psychological distress. When faced with SLE, patients have to implement coping strategies.
View Article and Find Full Text PDFJ Vet Intern Med
July 2019
Department of Medical Oncology, Oncovet, Villeneuve d'Ascq, France.
Background: Serum thymidine kinase 1 (sTK1) activity is closely correlated with DNA synthesis.
Objectives: Evaluate sTK1 activity as a biomarker for treatment response and early detection of relapse in dogs with lymphoma.
Animals: Ninety-seven client-owned dogs with naive or relapsed lymphoma and 23 healthy dogs.
Hematology
December 2019
i URC/CRC Groupe Hospitalier Paris Seine Saint Denis, APHP , Hôpital Avicenne , France.
Purpose: Subcutaneous immunoglobulin replacement therapy (IgRT) may be administered once a week with a pump or every other day with a syringe (rapid push). The objective of the study was to compare the impact of pump and rapid push infusions on patient's life quality index (LQI).
Methods: This study was a randomized, crossover, multicenter, non-inferiority trial conducted in adults with primary immunodeficiency (PID) accustomed to weekly infusions at home by pump.
Arthritis Res Ther
May 2018
Inserm U1132, Rheumatology Department, Lariboisière Hospital, Paris Diderot University, 2 rue Ambroise Paré, 75010, Paris, France.
Background: The uric acid (UA) level in patients with gout is a key factor in disease management and is typically measured in the laboratory using plasma samples obtained after venous puncture. This study aimed to assess the reliability of immediate UA measurement with capillary blood samples obtained by fingertip puncture with the HumaSens point-of-care meter.
Methods: UA levels were measured using both the HumaSens meter in the clinic and the routine plasma UA method in the biochemistry laboratory of 238 consenting diabetic patients.
Eur J Haematol
July 2018
URC/CRC Groupe Hospitalier Paris Seine Saint Denis, APHP, Hôpital Avicenne, Bobigny, France.
Patient Prefer Adherence
March 2018
Octapharma France, Boulogne, France.
Chest
January 2018
Université Paris-Sud, Faculté de Médecine, Université Paris-Saclay, Le Kremlin-Bicêtre; AP-HP, Centre de reference de l'Hypertension Pulmonaire, Service de Pneumologie, DHU Thorax Innovation, Hôpital Bicêtre, Le Kremlin-Bicêtre; INSERM UMR_S999, LabEx LERMIT, Centre Chirurgical Marie-Lannelongue, Le Plessis-Robinson, France.
Background: Pulmonary arterial hypertension (PAH) is a rare complication of systemic lupus erythematosus (SLE).
Methods: We identified all patients with SLE and PAH (SLE-PAH) who were enrolled in the French Pulmonary Hypertension Registry with a diagnosis confirmed by right heart catheterization (RHC). A control group of 101 patients with SLE without known PAH was selected from SLE expert centers participating in the Pulmonary Hypertension Registry.
Arthritis Care Res (Hoboken)
June 2018
Fédération de Rhumatologie, Hôpital Lariboisière, Assistance Publique-Hôpitaux de Paris, Université Paris 7, UFR médicale, and INSERM UMR1132, Hôpital Lariboisière, Paris, France.
Objective: In real life, in a substantial proportion of gouty patients receiving urate-lowering therapy (ULT), urate levels are not maintained below the target of 6.0 mg/dl. We aimed to search for factors associated with poor control of serum uric acid (UA) levels in a large population of patients with gout receiving ULT.
View Article and Find Full Text PDFPatient Prefer Adherence
July 2017
Renal Transplantation and Clinical immunology Department, University Hospital Centre of Tours, Tours, France.
Objective: To assess quality of life and satisfaction regarding immunoglobulin-replacement therapy (IgRT) treatment according to the route (intravenous Ig [IVIg] or subcutaneous Ig [SCIg]) and place of administration (home-based IgRT or hospital-based IgRT).
Subjects And Methods: Children 5-15 years old treated for primary immunodeficiency disease (PIDD) with IgRT for ≥3 months were included in a prospective, noninterventional cohort study and followed over 12 months. Quality of life was assessed with the Child Health Questionnaire - parent form (CHQ-PF)-50 questionnaire.
Arch Pediatr
January 2017
Soladis clinical studies, 84, boulevard du Général-Leclercq, 59100 Roubaix, France.
Background And Aims: The supine sleeping position with the head higher than the legs has no impact on regurgitations in infants. Inclined ventral decubitus decreases regurgitations but is associated with an increased risk of sudden infant death syndrome (SIDS). The LUNE study aimed to evaluate the impact of regurgitations on the choice of sleeping position by pediatricians and parents.
View Article and Find Full Text PDFOrphanet J Rare Dis
June 2016
Internal Medicine and Infectious Diseases Department, University Hospital Centre of Reims, avenue du Gal Koenig, 51092, Reims cedex, France.
Background: IgG replacement therapy (IgRT) in primary immunodeficiencies (PID) is a lifelong treatment which may be administered intravenously (IVIg) or subcutaneously (SCIg), at hospital or at home. The objective of the VISAGE study was to investigate if route and/or place for IgRT impact patients' satisfaction regarding IgRT and quality of life (QoL) in real-life conditions.
Methods: The study enrolled PID patients at least 15 years old receiving IgRT for at least 3 months.
Ann Rheum Dis
August 2016
Faculté de Médecine, Université Paris-Sud, Le Kremlin-Bicêtre, France AP-HP, Service de Pneumologie, DHU Thorax Innovation, Hôpital Bicêtre, Le Kremlin-Bicêtre, France INSERM U999, Centre Chirurgical Marie-Lannelongue, LabEx LERMIT, Le Plessis-Robinson, France.
Objectives: Despite the wide use of the 6 min walk distance (6MWD), no study has ever assessed its validity as a surrogate marker for haemodynamics and predictor of outcome in isolated pulmonary arterial hypertension associated with systemic sclerosis (SSc-PAH). We designed this work to address this issue.
Methods: Treatment-naïve patients with SSc-PAH were prospectively included from two sources: the French PAH Network (a prospective epidemiological cohort) (n=83) and randomised clinical trials submitted for drug approval (Food and Drug Administration) (n=332).