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NCT ID: NCT04833855 Completed - Clinical trials for Chronic Spontaneous Urticaria

Study to Evaluate Tezepelumab in Adults With Chronic Spontaneous Urticaria

INCEPTION
Start date: April 15, 2021
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the effect of tezepelumab on improvement in the Urticaria Activity Score over 7 days (UAS7).

NCT ID: NCT04832490 Completed - Clinical trials for Wounds and Injuries, Feet

ULD-E (Ultra Low Dose Extremities)

ULD E
Start date: February 1, 2018
Phase:
Study type: Observational

extremity trauma is a frequent reason for emergency room visits. There is an increase in the use of CT scanners in extremity trauma, due to a greater sensitivity of detection than X-rays, particularly for "occult fractures" and for the organization of treatment, particularly surgical treatment. As the number of CT scans increases, the reduction of the delivered dose has become a subject of interest. Among the many methods used, the use of iterative reconstruction has enabled a substantial reduction in the delivered dose without compromising image quality: low-dose and ultra-low-dose protocols (effective dose equivalent to the effective dose of the Diagnostic Reference Levels of radiographs from the same region of interest) have been developped, but have not yet been evaluated in extremity trauma. The subject of our feasibility study is to evaluate the diagnostic performance of ultra-low dose CT compared to radiographs in patients consulting for extremity trauma in the emergency room. The recent implementation in our department of a scanner dedicated to low-dose explorations as well as the optimization of protocols has allowed the realization of ultra-low-dose scans since June 2017.

NCT ID: NCT04832373 Completed - Clinical trials for Cochlear Implantation

Assessment of the Acceptability of a Humanoid Robot at Home for Children With Cochlear Implants - H2R2

H2R2
Start date: September 17, 2021
Phase: N/A
Study type: Interventional

The quality of the rehabilitation of deafness in children with cochlear implantation is a major prognostic factor for the outcome on speech comprehension and oral expression. This rehabilitation is carried out cooperatively by the hospital cochlear implantation team, and by a speech therapist located near the child's home. The multi-weekly sessions represent a constraint for the child and his parents. Complementary training work at home would make it possible to balance the equity in the distribution of care in the territory, and should promote the progress of the child, who is more inclined to use a tool available at home.

NCT ID: NCT04832022 Completed - COVID-19 Clinical Trials

Longitudinal Follow-up of Patients With Chronic Inflammatory Rheumatisms (CIRs) Vaccinated Against COVID-19 Compared to Patients Refusing Vaccination

COVID-RIC3
Start date: April 7, 2021
Phase:
Study type: Observational

To date, studies on SARS-CoV2and vaccines have been mostly from the general population not exposed to immunosuppressants. The efficacy and safety of COVID-19 vaccines need to be evaluated in these populations.

NCT ID: NCT04829812 Completed - Clinical trials for Peripheral Arterial Disease

Medical Compression in Patients With Chronic Wound and Peripheral Arterial Disease

COMPAD2
Start date: March 15, 2021
Phase:
Study type: Observational

Real-life practice survey of vascular specialist in France caring for patients with chronic wound for which compression treatment would be indicated and arterial disease of the lower limbs

NCT ID: NCT04829578 Completed - Clinical trials for Chronic Idiopathic Pruritus

Hypnosis for Chronic Idiopathic Pruritus

Start date: April 13, 2021
Phase: N/A
Study type: Interventional

Chronic idiopathic pruritus (CIP) is a frequent and disabling condition, for which there is no specific treatment. It was shown previously that hypnosis can relieve painful sensations. Pain and pruritus share many similarities regarding sensory receptors and pathways, suggesting that hypnosis might help relief CIP.

NCT ID: NCT04828928 Completed - Clinical trials for Wild-type Amyloid Cardiopathy

Neuropathy in Patients Monitored for Wild-type TTR Cardiac Amyloidosis (Non-mutated)

N-SAC
Start date: March 23, 2021
Phase: N/A
Study type: Interventional

Transthyretin (TTR) amyloidosis is a rare disabling disorder that can be hereditary or sporadic. Depending on the form, various tissues are affected. While in hereditary cases, neuropathy is predominant, cardiac impairment is the main manifestation in the sporadic form. The main objective of this project is to evaluate the proportion of patients with neuropathy in a population of patients with a non-mutated TTR amyloid cardiopathy condition.

NCT ID: NCT04828590 Completed - Clinical trials for Coronary Artery Disease

The ADAPT Study: Assessment of the DiAgnostic Performance of DeepVessel FFR in SuspecTed Coronary Artery Disease

ADAPT
Start date: August 10, 2020
Phase:
Study type: Observational

DEEPVESSEL FFR is a medical device that is designed to extract three- dimensional coronary tree structures and generate computed tomography-derived fraction flow reserve (FFR) values from coronary CT angiogram images. The primary objective of this multi-center clinical validation study is to validate the clinical performance of DEEPVESSEL FFR in identifying patients with myocardial ischemia due to significant obstructive coronary artery diseases.

NCT ID: NCT04827329 Completed - Clinical trials for Restless Legs Syndrome

Anesthetic Management of Patients With Chronic Sleep Disorders

ANEST-SLEEP
Start date: March 1, 2021
Phase:
Study type: Observational

The aim of this study is to describe and compare the anaesthesia history and possible problems encountered in 3 groups of patients with 3 chronic sleep diseases: narcolepsy, idiopathic hypersomnia, and restless legs syndrome followed at the Montpellier Sleep Unit. For each participant, existing data from the medical record will be used, with their consent. All participants will complete a standardized questionnaire, concerning their history of anaesthesia, the course and possible complications, and questions about their treatment for their sleep disorder.

NCT ID: NCT04827160 Completed - Covid19 Clinical Trials

Prediction of Thrombosis Using D-dimer Trends in COVID-19

TRENDS
Start date: March 2, 2020
Phase:
Study type: Observational

A high incidence of venous thromboembolic events (VTE) has been demonstrated in COVID-19. This incidence correlates with disease severity. Activation of coagulation secondary to sepsis combined with classical thrombotic risk factors may contribute to this prothrombotic state. Since the beginning of March 2020, the issue of venous thrombosis during SARS-CoV-2 infection has rapidly emerged as a major medical challenge since a significant rate of patients were thrombosing, some of them in spite of a well conducted preventive anticoagulation. Although D-dimers have been shown to be useful in identifying patients at risk of severe COVID-19 and even mortality, they cannot be used for diagnostic exclusion of pulmonary embolism. Indeed, since D-dimer levels rise non-specifically during infectious states, the exclusion threshold of 500 ng/ml cannot be used. It would therefore be useful to study the predictive value of D-dimers for thrombosis in COVID-19 patients.