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NCT ID: NCT05615181 Completed - Trismus Clinical Trials

Evaluation of the French Translation of Gothenburg Trismus Questionnaire (GTQ)

TRISMUS
Start date: December 22, 2020
Phase:
Study type: Observational

A monocentric Study to evaluate the french translation of Gothenburg Trismus Questionnaire (GTQ).

NCT ID: NCT05614895 Completed - Clinical trials for Bacterial Infections

A Study to Investigate the Pharmacokinetics of RO7223280 in Critically Ill Participants With Bacterial Infections

Start date: December 3, 2022
Phase: Phase 1
Study type: Interventional

The main aim of the study is to investigate the plasma pharmacokinetics (PK) and safety of intravenous (IV) administration of a single dose of 400 milligrams (mg) or 600 mg RO7223280 in critically ill participants with bacterial infections.

NCT ID: NCT05614739 Recruiting - Neoplasm Metastasis Clinical Trials

A Study of LOXO-435 in Participants With Cancer With a Change in a Gene Called FGFR3

Start date: January 12, 2023
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to learn more about the safety, side effects, and effectiveness of LOXO-435. LOXO-435 may be used to treat cancer of the cells that line the urinary system and other solid tumor cancers that have a change in a particular gene (known as the FGFR3 gene). Participation could last up to 30 months (2.5 years) and possibly longer if the disease does not get worse.

NCT ID: NCT05614635 Completed - Edentulous Mouth Clinical Trials

Safety and Technical Performance of Plastalgin and Plastalgin Fast in Patients Requiring a Dental Impression

Start date: October 12, 2022
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to gather clinical data related to the use of Plastalgin and Plastalgin Fast, in order to comply with the new medical device regulation. The target population for this study is the same as the intended population specified in the study device's instructions for use: children from 5 years old and adults. Collection, recording, and reporting of data will be accurate and will ensure the privacy, health, and welfare of participating patients during and after the study

NCT ID: NCT05614336 Recruiting - COVID-19 Clinical Trials

COVID-19 Antibody Responses in Cystic Fibrosis

CAR-CF
Start date: June 15, 2022
Phase: N/A
Study type: Interventional

Coronavirus disease 2019 (COVID-19) which is caused by the virus SARS-CoV-2 has resulted in an ongoing global pandemic. It is unclear whether the relatively low number of reported cases of COVID-19 in people with CF (pwCF) is due to enhanced infection prevention practices or whether pwCF have protective genetic/immune factors. This study aims to prospectively assess the proportion of pwCF, including both adults and children with CF who have evidence of SARS-CoV-2 antibodies over a two-year period. This study will also examine whether pwCF who have antibodies for SARS-CoV-2 have a different clinical presentation and what impact this has on their CF disease. The proposed study will recruit pwCF from paediatric and adult CF centres in Europe. Serological testing to detect antibodies will be performed on blood samples taken at month 0, 6, 12, 18 and 24 with additional time-points if bloodwork is available via normal clinical care. Clinical data on, lung function, CF-related medical history, pulmonary exacerbations, antibiotic use, and microbiology and vaccination receipt, will be collected during routine clinical assessments. Associations will be examined between socio-demographic and clinical variables and serologic testing. The effects of SARS-CoV-2 infection on clinical outcomes and analyse end-points will be examined to explore any age-related or gender-based differences, as well as subgroup analysis of outcomes in lung-transplant recipients and pwCF receiving CFTR modulator therapies. As pwCF receive COVID-19 vaccination a comparison of the development and progression of anti-SARS-CoV-2 antibodies in pwCF following natural infection and vaccination SARS-CoV-2 over time will be performed

NCT ID: NCT05613868 Recruiting - Clinical trials for Aicardi-Goutières Syndrome (AGS)

TPN-101 in Aicardi-Goutières Syndrome (AGS)

Start date: March 15, 2023
Phase: Phase 2
Study type: Interventional

A phase 2a multi-center, open-label single dose level study of TPN-101 in Patients with Aicardi-Goutières Syndrome (AGS)

NCT ID: NCT05613712 Recruiting - Clinical trials for Chronic Inflammatory Disease

Chronic Inflammatory Rheumatism: Management of Comorbidities in Ambulatory Medicine

SCORIC-A
Start date: February 11, 2023
Phase:
Study type: Observational

Identification of factors limiting compliance with the recommendations established during the evaluation of the SCORIC population by the rheumatology department of the CHU Grenoble Alpes

NCT ID: NCT05613647 Recruiting - Shock Clinical Trials

Concordance Study of Therapeutic Decision-making in Patients With Shock Based on Hemodynamic Monitoring

PICC-ECHO
Start date: December 13, 2022
Phase:
Study type: Observational [Patient Registry]

Shock is a serious complication corresponding to acute circulatory failure resulting in multiorgan failure and death. In order to improve cellular oxygen utilization, several therapies can be used. To select one of them, the monitoring of cardiac output is helpful. However, there are several methods used in current practice in intensive care for evaluating hemodynamic. Currently, in patients with acute circulatory failure, no study has compared the concordance of therapeutic decision-making based on transpulmonary thermodilution or transthoracic echocardiography. The objective of the PICC-ECHO study is thus to assess the concordance of therapeutic decision-making by several experts, based on data from transpulmonary thermodilution or transthoracic echocardiography. Indeed, the investigators hypothesize that performing hemodynamic monitoring based on transpulmonary thermodilution or transthoracic echocardiography does not lead to the same therapeutic management in patients in shock.

NCT ID: NCT05613530 Completed - Simulation Clinical Trials

Mobile Application as a Clinical Decision Support Tool for Neonatal Resuscitation in the Delivery Room

MAXnéonat
Start date: May 19, 2021
Phase: N/A
Study type: Interventional

The need for neonatal cardiopulmonary resuscitation in the delivery room is rare with less than 1% of newborns requiring advanced resuscitation. The use of clinical decision support tools to guide practitioners on medical procedure steps is recognized by the medical community. In this randomized bi-centric controlled study, we investigate the effect of a mobile phone application on technical and non-technical performance of student trinomials managing simulated critical neonatal events

NCT ID: NCT05613517 Completed - No Eye Disorder Clinical Trials

Study of the Angle Lambda and Ocular Dominance

EPOLAF
Start date: November 25, 2022
Phase:
Study type: Observational

Anatomical ophthalmological connections and their dynamics are still debated in the scientific community. However, their considering is essential in many surgeries (strabismus, cataract, refractive...) or in clinical practice. The correlation between these biometric values would make it possible to refine the knowledge related to these landmarks and thus offer better ophthalmological management by integrating these variables into the clinical examination. The aim of the study is to analyze the correlation between the angle lambda and the ocular dominance depth in healthy individuals without ophthalmologic disorder. Then, seconds goals were defined as the study of the relation between the value of the angle lambda and the fixation disparity quantified with the Rousseau test. Relation between ocular dominance measured with the Guillon's test and the Hole-in-car test will also studied.