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NCT ID: NCT04548245 Recruiting - Clinical trials for Attention Deficit Disorder

Markers of Executive Attention Development in Preschoolers

MEDiATE
Start date: February 1, 2021
Phase:
Study type: Observational

This project aims to identify precursors of executive attention that can serve as early markers of ADD.

NCT ID: NCT04548141 Completed - Sedentary Behavior Clinical Trials

Quick Questionnaire to Evaluate Physical Activity

SAPHIR
Start date: November 26, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to test and validate a new questionnaire (SAPHIR) in order to get an evaluation of patients physical activity.

NCT ID: NCT04548050 Completed - Early Breastfeeding Clinical Trials

Impact of the Training of Nursing Staff on the Practice of Manual Expression of Early Colostrum in Neonatal Medicine

ORLIKID
Start date: September 14, 2020
Phase:
Study type: Observational

Colostrum is an irreplaceable nutrient rich in protein and antibodies. Its taste and smell are similar to those of amniotic fluid (therefore rich for the senses of the baby separated from his mother). It should be offered to every newborn baby, regardless of term and the type of breastfeeding their mom wants. The early expression of colostrum, within the first 2 hours after childbirth, is an essential way to start lactation of a mother separated from her baby. The sooner and more often the mother stimulates her breasts, the more milk she will have for her baby in the weeks to come. Manual expression of milk is therefore an essential gesture to initiate lactation, maintain it, and giving colostrum to babies as early as possible is beneficial. Two studies carried out in the neonatal medicine department of Felix Guyon Hospital in premature infants <33 week of amenorrhea (PRE'OLACT study in 2015-2016 by Dr RAJAOFERA and Diploma from university (DU) breastfeeding brief in 2018-2019 by Dr GRONDARD) found the same results: the desire for breastfeeding is 80% but manual expression of colostrum before H24 is only achieved by 30% of mothers and before H6 in only 6% of cases. .

NCT ID: NCT04548037 Terminated - Clinical trials for Amnesia, Transient Global

Assessment of Emotional Memory During Transient Global Amnesia

EMOTICTUS
Start date: May 30, 2022
Phase:
Study type: Observational

There are few studies on the role played by emotions in transient global amnesia (TGA), in particular with regard to their impact on the functioning of memory. The study investigators wish to better understand the link between episodic memory, emotional state and psychogenic factors during TGA. It would be interesting to see if the patients suffering from TGA triggered by a psychological shock process emotional information differently from those whose TGA was triggered by an "organic" shock (physical effort, trauma, etc.). Finally, amnesic stroke is a good model for better understanding the function of the hippocampus, in particular of the CA1 region, in episodic memory.

NCT ID: NCT04547959 Active, not recruiting - Clinical trials for Cervical Disc Disease

Prospective Clinical Study to Evaluate the Efficacy of the Stand-alone Cervical Interbody Cage C-CURVE ( Titanium) Manufactured by MEDICREA®

C-CURVE
Start date: November 20, 2020
Phase: N/A
Study type: Interventional

This study includes one type of product named C-CURVE which is a Stand-alone Cervical Interbody Cage. This product is available in two materials: PEEK and Titanium. The C-Curve Cervical Interbody Devices is one single implant used for insertion between two adjacent vertebrae (cervical spine). C-Curve has been designed to restore and/or maintain adequate interbody height, and thus help stabilize one or more cervical levels while fusion occurs. This system has also as objectives to increase of the quality of life, decrease patient's pain and decrease a potential dysphagia (clinical performances). This system must only be used in the cervical spine. This post-market clinical follow-up (PMCF) study aims to confirm the acceptable benefits/risk profile of the device for the patients and to fill essential requirements to maintain the CE mark through a clinical evaluation.

NCT ID: NCT04547751 Completed - Drug Abuse Clinical Trials

Hospitalisations of Teenagers and Young Adulthoods in Mayotte After Consumption of an Illegal Drug Called " Chimique ", Which Substances Are Incriminated ? : HOMACHI

HOMACHI
Start date: June 6, 2020
Phase:
Study type: Observational

The study aims (i) to identify which substances leading to hospitalizations at Mayotte are also called "chimique" and (ii) to correlate these substances with clinical pictures in order to favor a better approach of the treatments.

NCT ID: NCT04547712 Active, not recruiting - Parkinson Disease Clinical Trials

Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease

ADAPT-PD
Start date: December 14, 2020
Phase: N/A
Study type: Interventional

The purpose of the study is to demonstrate the safety and effectiveness of adaptive DBS (aDBS) for Parkinson's disease.

NCT ID: NCT04547595 Recruiting - Knee Osteoarthritis Clinical Trials

Hypnosis Intervention for the Management of Pain Perception During Joint Lavage

HypnoArt
Start date: October 6, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether hypnosis intervention added to usual care is more effective than usual care alone to control pain during lavage procedure in patients with knee osteoarthrosis

NCT ID: NCT04547569 Completed - Motor Activity Clinical Trials

Somesthesic Role of the Ventro-lateral Prefrontal Cortex in Speech Motor Learning

BRAVA²
Start date: October 20, 2020
Phase: N/A
Study type: Interventional

These studies test the hypothesis that frontal areas of the brain participate in the cortical networks involved in the somotosensory processing that happens during speech motor learning.

NCT ID: NCT04547543 Recruiting - Clinical trials for Obstructive Sleep Apnea

Follow-up of Apneic Patients by Visio-consultation

VISIOSAS
Start date: September 8, 2020
Phase: N/A
Study type: Interventional

Prospective multicenter open-label randomized clinical trial comparing videoconsultation to a face-to-face consultation during the follow-up of apneic patients treated by continuous positive pressure (CPAP) .