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NCT ID: NCT04829565 Recruiting - Rhizarthrosis Clinical Trials

Assessment of Pain After Intra-articular Botulinum Toxin Injections in Carpometacarpal Osteoarthritis of the Thumb

Start date: September 9, 2021
Phase: Phase 4
Study type: Interventional

Only 4 randomized controlled clinical trials have been published to date to assess the short-term effectiveness of intra-articular Botulinum Toxin injection on pain, function and quality of life in patients suffering from chronic knee pain related or not to knee osteoarthritis and also in the context of ankle osteoarthritis. The analgesic properties and the reported safety make intra-articular Botulinum toxin a strong candidate in the treatment of symptomatic manifestations of osteoarthritis disease and more particularly in certain locations such as the trapezo-metacarpal joint. Investigators hypothesize that injection of intra-articular Botulinum toxin into the trapezo-metacarpal joint will be of benefit in reducing pain and improving function in patients with rhizarthrosis. Investigators will begin a monocentric randomized controlled trial comparing intra-articular injections of Botulinum toxin and placebo.

NCT ID: NCT04829474 Terminated - Spouse Abuse Clinical Trials

Severe Women Injury Factors Test (SWIFT)

SWIFT
Start date: March 8, 2021
Phase:
Study type: Observational

Intimate partner violence is a real public health problem, and affects all socio-cultural backgrounds It is defined by behavior within an intimate relationship that causes physical, psychological or sexual harm or suffering to the people in that relationship. Several risk factors exist such as young age, low level of education, exposing to violence during childhood, pregnancy or addictions.

NCT ID: NCT04829175 Recruiting - Clinical trials for Pelvic Organ Prolapse

Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry

Start date: April 13, 2022
Phase:
Study type: Observational

The objective of this post market, clinical registry is to evaluate the performance of the products of the TVT family of products or vaginal vault or uterine prolapse repair (with laparotomic or laparoscopic approach including robotic assisted) using either Gynemesh PS Mesh or Artisyn Mesh in women undergoing surgery for SUI and POP.

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: NCT04828460 Recruiting - Covid19 Clinical Trials

Monitoring of COVID-19 Vaccine Response in Organ Transplant Patients

COVATRANS
Start date: February 9, 2021
Phase:
Study type: Observational

Vaccination against SARS CoV-2 appears to be the best strategy today to control the COVID-19 pandemic. The first published studies with Pfizer, Moderna and Astra-Zeneca vaccines show very good vaccine protection in the general population and good short-term tolerance. The efficacy of these vaccines ranges from 62 to 95%, which is particularly remarkable, especially for mRNA vaccines. Nevertheless, these studies do not report the vaccine response in organ transplant patients. It is known that transplant patients have lower vaccine responses than immunocompetent patients due to some degree of immunosuppression. Therefore, the investigators are interested in evaluating the vaccine response of organ transplant recipients after vaccination against SARS- CoV-2. For non-responder patients, new strategies can be proposed: 3rd or 4th boost of vaccine or perfusion/injection of antiS monoclonal antibodies. These strategies must be evaluated.

NCT ID: NCT04827758 Terminated - Sarcopenia Clinical Trials

Evaluation of a Screening Strategy for Sarcopenia: a Monocentric Prospective Cohort Study (STRAS)

STRAS
Start date: April 22, 2021
Phase: N/A
Study type: Interventional

The main objective of this study is to determine the prevalence of sarcopenia in patients hospitalized in the follow-up care and rehabilitation units of the geriatrics department of the Mulhouse French hospital.

NCT ID: NCT04827719 Active, not recruiting - Clinical trials for Acute Myeloid Leukemia

BST-236 as a Single Agent in Adults With Relapsed or Refractory AML or HR-MDS

Start date: May 1, 2021
Phase: Phase 2
Study type: Interventional

To assess the efficacy, and safety of BST-236 in patients unfit for intensive chemotherapy with AML or HR MDS that failed or relapsed following first line therapy

NCT ID: NCT04827576 Active, not recruiting - Solid Tumor Clinical Trials

Study of Magrolimab in Patients With Solid Tumors

ELEVATELung&UC
Start date: October 1, 2021
Phase: Phase 2
Study type: Interventional

The goals of this clinical study are to learn about the safety, tolerability, dosing and effectiveness of magrolimab in combination with docetaxel in patients with solid tumors.

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.