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NCT ID: NCT05231668 Recruiting - Clinical trials for Osteogenesis Imperfecta

Single Ascending Dose Study of SAR439459 in Adults With Osteogenesis Imperfecta (OI)

Start date: August 25, 2022
Phase: Phase 1
Study type: Interventional

SAR439459 is a human anti-Transforming growth factor β (TGFβ) monoclonal antibody. This phase 1 clinical study investigates the safety, tolerability, and activity of a single dose of SAR439459 in adult participants with OI. Participants will receive a single IV dose of SAR439459 with safety, pharmacokinetic (PK), and pharmacodynamic (PD) assessments over 24 weeks. There will be up to 3 dose cohorts. In addition to safety, tolerability, and PK assessments, bone mineral density (BMD) will be evaluated by dual-energy Xray absorptimetry (DXA) scan and a series of blood biomarkers will be monitored to document pharmacodynamic effects of the single dose of SAR439459.

NCT ID: NCT05231551 Recruiting - Infertility Clinical Trials

Using Embryo Organoids to Discover Human-specific Mechanisms of Preimplantation Embryo Development and Early Pregnancy

EMBRYOx
Start date: February 1, 2022
Phase:
Study type: Observational

EMBRYOx study aims to establish and validate the use of trophoblast organoids (embryoids) from trophoblast placental stem cells as a 3D research model in understanding further preimplantation embryo development in vitro. The organoids are capable of proliferation, differentiation, and implantation in a matrix, reproducing early human embryo development.

NCT ID: NCT05231525 Completed - Clinical trials for Neuromuscular Residual Curarization

Comparison of the TOFScan and the WiTOF During Recovery of Neuromuscular Function

Start date: March 9, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to compare two neuromuscular blockade monitors on recovery from an ATRACURIUM intra veinous injection for surgery. The TOFscan, a wired connected monitors and the WiTOF, a wireless connected monitor.

NCT ID: NCT05231486 Recruiting - Clinical trials for Developmental Coordination Disorder

Effectiveness of the COOP Group Approach for Children With Developmental Coordination Disorder (DCD)

ECOOPG
Start date: January 4, 2023
Phase: N/A
Study type: Interventional

Developmental Coordination Disorder (DCD) is a neurodevelopmental disorder that causes difficulty in motor coordination both in their learning and in their execution. This disorder affects about 5% of school-age children. The Cognitive Orientation to daily Occupational Performance (CO-OP) approach is a non-drug intervention technique, focused on solving motor problems where the patient is taught cognitive strategies (in small groups) with a view to acquire and execute motor coordination effectively. It is part of Cognitive-Behavioral techniques (CBT). This is one of the approaches recommended internationally and in France for patients with Developmental Coordination Disorder. In addition, for DCD patients, non-drug interventions in small groups are recommended internationally for this condition. However, few studies are available to validate the CO-OP approach in this format. Since 2013, the Department of Child and Adolescent Psychological Medicine sector 2 (MPEA2) of the University Hospital of Montpellier has offered group interventions for children diagnosed with DCD who are referred to them in current care practice with the CO-OP approach. In view of the major repercussions of DCD on self-esteem, academic and academic success and the development of social ties, this group therapy will restore a life trajectory and improve the quality of life of these patients.

NCT ID: NCT05231447 Not yet recruiting - Clinical trials for Congenital Abnormalities

Birth Defect Registry in South West Region of France

ATENA
Start date: March 1, 2022
Phase:
Study type: Observational [Patient Registry]

Regional population-based registry for the epidemiological surveillance of congenital anomalies

NCT ID: NCT05231265 Recruiting - Low Back Pain Clinical Trials

Effect of Lumbar Surgery on Complexity During a Walking Task in Chronic Low Back Pain

LOBAFRACS
Start date: October 16, 2023
Phase:
Study type: Observational

Lumbar surgery is the most common treatment for chronic disabling low back pain with degenerative disc disease. There are few elements to objectively evaluate the improvement of the motor control after surgery and the motor adaptation capacities of the patients. The impact of lumbar surgery on complexity in this painful context has never been studied. Theoretically, the restriction of mobility imposed by lumbar surgery should limit the subject's adaptive capacities (of one or more lumbar segments) and thus reduce complexity. Nevertheless, improvement in pain intensity levels could allow the patient to find better motor adaptation capacities, necessary for a positive evolution in the long-term. The aim of this study was to investigate the evolution of gait complexity in chronic low back pain patients pre- and post-surgery. If surgery improves the adaptability of walking through an antalgic benefit exceeding the induced stiffness, the complexity of walking should be superior after surgery. This is a proof-of-concept study in which the study investigators hypothesize that measuring complexity by fractal analysis during a walking task will show the increase in gait complexity induced by lumbar surgery at 3 and 6 months after surgery.

NCT ID: NCT05230992 Completed - Nodule Clinical Trials

Optimization of the Sensitivity of Histological Diagnosis of Pulmonary Nodules

CRYOPROBE
Start date: November 5, 2022
Phase: N/A
Study type: Interventional

In pulmonary oncology, the diagnosis of medium-sized pulmonary nodules (10 to 20 mm), too distal to be reached by standard bronchial fibroscopy but remaining proximal, is difficult. There are 2 techniques: transthoracic puncture-biopsy under CT scan, usually performed by radiologists, and distal sampling guided by radial ultrasound mini-probe. The limitations of the last technique could be overcome by the use of cryoprobes for sampling, as they would take more tissue by freezing.

NCT ID: NCT05230875 Recruiting - Ulcerative Colitis Clinical Trials

Sexual Dysfunction Among Inflammatory Bowel Disease Adults-Clinical Trial

SexIA-CT
Start date: April 7, 2022
Phase:
Study type: Observational

Patients with Inflammatory Bowel Disease (IBD) have higher rates of sexual dysfunction than the general population. We offer an educational program on IBD including a specific discussion on intimacy and sexuality for IBD patients. Our objective is to investigate the benefit of this intervention on sexual function in patients with IBD.

NCT ID: NCT05230524 Recruiting - Clinical trials for Paroxysmal Atrial Fibrillation

DIAMOND AF Post-Approval Study

DAF PAS
Start date: February 28, 2022
Phase:
Study type: Observational

The DIAMOND AF Post Approval study is a prospective, global, multi-center, non-randomized, single-arm observational trial

NCT ID: NCT05230498 Recruiting - Clinical trials for Sensorineural Hearing Loss, Bilateral

Study of Sound and Speech Perception in New Cochlear Implanted Subjects Using or Not an Anatomy-based Fitting

Start date: February 15, 2022
Phase: N/A
Study type: Interventional

Main objective: Compare the recognition of environmental sounds with an anatomy-based fitting and with a default fitting adult patients newly implanted with a MED-EL cochlear implant. Secondary objectives: Compare speech recognition in quiet with an anatomy-based fitting and with a default fitting in adult patients newly implanted with a MED-EL cochlear implant. Compare speech recognition in noise with an anatomy-based fitting and with a default fitting in adult patients newly implanted with a MED-EL cochlear implant.