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NCT ID: NCT04688827 Not yet recruiting - Heart Failure Clinical Trials

Impact of Additional Resistance Training During Rehabilitation Therapy in Patients With Heart Failure

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

The impact of moderate- or low-intensity resistance training will be investigated additional to endurance training in heart failure patients following rehabilitation. The aim is to optimize intensity of resistance training in this patient population.

NCT ID: NCT04701840 Not yet recruiting - Clinical trials for Major Depressive Disorder

Accelerated TBS for Adolescent Suicidal Ideation

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

The purpose of this study is to gather information regarding the use of a new type of transcranial magnetic stimulation (TMS) called theta burst stimulation (TBS) for suicidal ideation in adolescents with Major Depressive Disorder (MDD). The investigators hope to learn if this TMS treatment improves suicidal ideation over 10 days and clinical outcomes over 1 year of follow-up.

NCT ID: NCT04716543 Not yet recruiting - Covid19 Clinical Trials

Epidemiological Investigation of COVID-19 in Laos Using a One-Health Approach in Human and Animals

LACOVISS
Start date: August 1, 2021
Phase:
Study type: Observational

The Respiratory infection COVID-19, due to a new coronavirus, SARS-CoV2, appeared in December 2019 in several people who attended the wildlife market in Wuhan, Hubei Province, China. While COVID-19 has spread to nearly 200 countries and caused two millions infections, Lao PDR detected its first confirmed case very recently, on March 20, three months after the start of the outbreak in China. As of April 12th, 2020, Lao PDR has only recorded 18 confirmed cases, a very low number compared to other countries around the world. However, several key factors suggest that Lao PDR could be much more affected by COVID-19 because of the following reasons: (i) The multiple and massive trans-border movements between Lao PDR and China. (ii) The similar biogeographical and socio-ecological characteristics with South-Western China. (iii) The detection of a high diversity of Betacoronavirus sequences in several species of bats in Lao PDR. (iv) The numerous markets selling high volumes of local wildlife including bats and pangolins. LACOVISS project aim at investigating, using a ONE-HEALTH approach, this unexpected epidemiological pattern of SARS-CoV-2 in Lao PDR by bringing together an interdisciplinary team of experts in the field from IRD, the University of Caen, the Center of Infectiology Lao-Christophe Mérieux (CILM) and the National animal Health Laboratory (NAHL) in Vientiane. The study will focus on a community-based cohort of 1092 households, including 5400 study participants, followed-up between March 2015 and February 2019 for influenza-like illness investigation and causative agents detection (LACORIS project), located in the Vientiane metropolitan area. The COVID-19 progression in Lao PDR, and track SARS-CoV-2, will be followed retrospectively and prospectively, in all potential actors in SARS-CoV-2 circulation, including humans, domestic animals, and wildlife. The LACOVISS project will undoubtedly bring new insight in SARS-Cov-2 and SARS-CoV-like circulation in Lao PDR as well as valuable information on the natural history of COVID-19, and on the modalities of the spillover into humans, which are still largely unknown.

NCT ID: NCT04725019 Not yet recruiting - Cerebral Palsy Clinical Trials

Enhancing Motor Learning in Children With Cerebral Palsy Using Transcranial Direct-current Stimulation

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

The goal of this study is to test the effects of transcranial direct current stimulation (tDCS) on motor learning and brain plasticity in children with unilateral spastic cerebral palsy (USCP).

NCT ID: NCT04765904 Not yet recruiting - Clinical trials for Early Childhood Caries

Clinical Efficiency and Treatment Failure of Hall Versus SDF Techniques in the Management of Carious Primary Molar.

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

This study will compare two non- invasive treatment options: Hall technique and 38% Silver diamine fluoride. Both are methods used to create a more favorable environment without removal of caries leading to the arrest of the progression of demineralization process and restoring the function of the diseased molars.

NCT ID: NCT04779034 Not yet recruiting - Clinical trials for Heart Rate Variability

The Relationship Between Heart Rate Variation and Athletic Performance in Basketball Players

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

This study was planned to explain the relationship between heart rate variability and their sportive performance in basketball players.

NCT ID: NCT04786678 Not yet recruiting - Stress Clinical Trials

Sensible Sleep: Measuring Alarm and Snooze Behavior in Teens Using Wearables and Smartphones

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

Pilot data suggests that working professionals and college students routinely use alarms and snooze. Alarm usage and snoozing is associated with several negative health biomarkers including lighter sleep, higher resting heart rate, and reduced sleep duration. It is unclear when this behavior is established, but it is likely in the teenage years when chronic sleep restriction begins to effect a large percentage of Americans. We will ask teens about psychological traits (e.g. personality) and snoozing behavior in a repeated measures design. In addition, we will implement a smartphone based intervention which notifies teens when they are awake past their minimum bedtime for adequate sleep. throughout the study, we will monitor sleep and heart-rate via wearable. From this data, we will establish the prevalence of alarm and snoozing behaviors in teens. We will determine what demographic, psychological, and behavioral traits predict snoozing, and if there are any differences in health biomarkers (e.g. sleep duration, resting heart rate)between snooze and/or alarm users. We will use data from the wearables and smartphones to generate features that can detect snoozing, and will validate them against self-report. Finally, we seek to determine if alarm and snoozing behavior can be reduced via a smartphone intervention aimed at increasing sleep duration.

NCT ID: NCT04807010 Not yet recruiting - Clinical trials for Benign Prostatic Hyperplasia

PROARTE -PROstate ARTery to Reduce the Symptoms of Benign Prostatic Hyperplasia

PROARTE
Start date: August 1, 2021
Phase: Phase 3
Study type: Interventional

This is a trial to demonstrate the superiority of prostate artery embolization (PAE) over sham procedure in men with benign prostatic hyperplasia (BPH) induced lower urinary tract symptoms (LUTS). The trial will aim to enroll 108 patients at a 2:1 allocation over a 2 year period.

NCT ID: NCT04818567 Not yet recruiting - Clinical trials for ERCP, Failure, Complications, Cannulation

Frequency and Causes of Failed Endoscopic Retrograde Cholangio-Pancreatography in AL-Rajhi Endoscopy Unit

Start date: August 1, 2021
Phase:
Study type: Observational

The failure can be traced backed to operator causes, technical causes and patient causes. the most common etiology is cannulation failure. ERCP complications includes post-ERCP pancreatitis, perforation, bleeding, cholangitis and cholecystitis.

NCT ID: NCT04837599 Not yet recruiting - Colonic Polyp Clinical Trials

Artificial Intelligence Performance in Colonoscopy in Daily Practice

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

randomized, controlled single center, single investigator study mainly in colorectal screening population in daily practice with and without artificial intelliegence (AI) named DiscoveryTM from Pentax medical. Patient randomly are allocated to one of four groups: Pentax i10 colonoscopes without any additional device, Pentax i 10 with DiscoveryTM (AI), Pentax i 10 with EndocuffTM and Pentax i10 with EndocuffTM and DiscoveryTM (AI). The different groups are compared in terms of the different parameters: e.g. time of endoscopy, polyps (PDR) and adenoma detected (ADR).