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NCT ID: NCT05311865 Completed - Healthy Participant Clinical Trials

Transmission of Covid-19 During Clubbing Events in Closed Places

ITOC
Start date: September 4, 2021
Phase: N/A
Study type: Interventional

The ITOC study is a cluster randomised, controlled, multicentre trial in Paris region, France. The intervention is an 8-hour indoor clubbing event with no mask wearing, no social distancing, at maximum room capacity. 1,200 healthy volunteers aged 18-49 years and fully vaccinated will be included. Participants are recruited by group of up to 10, to be randomized 2:1 to experimental group (800 volunteers in a venue ) or control group (400 volunteers asked to stay at home). All participants will provide a salivary sample the day of experiment and seven days later. Participants will also answer surveys on the social and psychological impact of lockdown and indoor club closing, attitude towards vaccination, behaviour at risk of COVID-19 transmission during the day of the event (for both groups) as well as follow-up surveys on symptoms that participant may experience. Virological analyses include polymerase chain reaction (PCR) of salivary samples and air of the venue, investigating SARS-CoV-2 PCR.

NCT ID: NCT05311800 Completed - Clinical trials for Overweight and Obesity

High-Intensity Interval Training and Fat Mass Losses

RIESLING
Start date: September 1, 2021
Phase: N/A
Study type: Interventional

The aims of this study was to compare two isoenergetic HIIT (High-intensity Interval training) programs (cycling vs. running) on body composition, substrate oxidation at rest and during a moderate exercise, muscle functionality, glycaemic control, lipid profile, inflammation, maximal aerobic capacity (VO2max) and gut microbiota composition in men with overweight or obesity. The investigators hypothesized that both programs could decrease total, abdominal and visceral fat mass but due to differences in muscle solicitation, metabolism adaptation and blood flow, and that running could favors greater fat mass losses.

NCT ID: NCT05311241 Completed - Telemedicine Clinical Trials

Teleconsultation in Ambulatory Care in France

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

Teleconsultation is a telemedicine medical act carried out remotely via information and communication technologies. This medical procedure has been legal in France since 2010 and reimbursed by the National Health Insurance under certain conditions since 2018. In 2020, following the COVID-19 epidemic, the lockdowns and the extension of the scope of financial coverage, 17 million teleconsultations have been reimbursed. To date, few scientific studies have been published in France to precisely describe the use of the service giving access to outpatient teleconsultation, in particular since the major increase in activity linked to the COVID-19 epidemic. The objective is to describe the use of the service giving access to outpatient teleconsultation carried out in France by teleconsultation companies and compare the use of the teleconsultation service according to the medical density of the territory.

NCT ID: NCT05310617 Completed - Infertility Clinical Trials

Parental Project and Premature Ovarian Insufficiency

ParentIOP
Start date: June 20, 2022
Phase:
Study type: Observational

One of the main repercussions of POI is infertility. When the diagnosis of POI is announced, the question of fertility is addressed and the patient is often directed towards egg donation or adoption when she has a parental project. However, there are cases of spontaneous pregnancies after diagnosis. This study was conducted to determine the proportion of patients with POI who were able to realize a parental project after diagnosis in the long term and by what means.

NCT ID: NCT05309980 Completed - Cardiogenic Shock Clinical Trials

Outcomes in CArdiogenic SHock Patients Treated by MEchanical Circulatory suppoRt devicE : Impact of Shock Team

CASHMERE
Start date: April 1, 2021
Phase:
Study type: Observational

In this before-after monocenter study, the authors teste the hypothesis that the implementation of a dedicated shock team could improve the outcome of patients with refractory cardiogenic shock assisted by mechanical circulatory support.

NCT ID: NCT05308433 Completed - Healthy Clinical Trials

Cybersickness imAgiNg Olfactory Evocation

CANOE
Start date: April 13, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to, using fMRI, compare brain activations during olfactory imagery induced by different visual supports (words, pictures, colors and colored arrangements) in healthy subjects. This will allow us to choose the best olfactory imagery facilitator and to assess its effect on cybersickness.

NCT ID: NCT05308355 Completed - Thoracic Surgery Clinical Trials

Opioid-free Anesthesia and Thoracoscopy Surgery

OFAT
Start date: April 4, 2022
Phase:
Study type: Observational

Evaluation of a service OFA (Opioid-free Anesthesia) protocol on post-operative pain of patients operated on by video-thoracoscopic carcinologic surgery by counting them to a group of patients receiving standard general anesthesia with opioid.

NCT ID: NCT05307601 Completed - COVID-19 Clinical Trials

Immune Response Following COVID-19 in Hemodialysis Patients

IMMUNOVIDIAL
Start date: September 1, 2020
Phase:
Study type: Observational

Patients with chronic kidney disease (CKD), particularly those undergoing hemodialysis (HD), are at high risk of a severe form of COVID-19. This study aims to characterize the inflammatory and antiviral response during SarsCov2 infection in adult

NCT ID: NCT05306717 Completed - Clinical trials for Psychiatric Disorder

Impact of the Preventive Emotions Management Questionnaire on the Rates of Isolation and Mechanical Restraint Measures in the Psychiatric Admission Unit

PACT
Start date: April 1, 2022
Phase:
Study type: Observational

This observational study assesses whether the use of the QPGE has an impact on the rates of isolation and mechanical restraint in adult psychiatric admission units. It is supplemented by a qualitative survey that will collect the experience of caregivers using the QPGE.

NCT ID: NCT05306262 Completed - Hypnosis Clinical Trials

Interest of Catalepsy in the Hypnotic Trance

CATALHYPNOANI
Start date: May 26, 2022
Phase: N/A
Study type: Interventional

Catalepsy seems to facilitate hypnotic induction and deepen hypnotic trance, although no work confirms the usefulness of this technique which is in common use in hypnosis. Furthermore, it has been shown that the hypnotic trance state is accompanied by an increase in parasympathetic tone, the non-invasive measurement of which is easy by the ANI monitor (Analgesia Nociception Index). The research hypothesis is that, by adding a body dissociation, catalepsy could facilitate and intensify the hypnotic trance, the intensity of which can be monitored and is proportional to the parasympathetic tone.