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NCT ID: NCT04652700 Completed - Clinical trials for HIV Preexposure Prophylaxis

Oral Islatravir (MK-8591) Once-Monthly as Preexposure Prophylaxis (PrEP) in Men and Transgender Women Who Are at High Risk for HIV-1 Infection (MK-8591-024)

Impower-024
Start date: March 15, 2021
Phase: Phase 3
Study type: Interventional

The main purpose of the study is to evaluate the safety and tolerability of oral Islatravir (ISL) once monthly (QM) as Preexposure Prophylaxis (PrEP) in cisgender men who have sex with men (MSM) and transgender women (TGW) who have sex with men and who are at high risk of HIV-1 infection with 48 or 96 weeks of treatment and a minimum follow-up of 42 days.

NCT ID: NCT04652518 Terminated - Covid19 Clinical Trials

LYT-100 in Post-acute COVID-19 Respiratory Disease

Start date: December 11, 2020
Phase: Phase 2
Study type: Interventional

This study is being conducted in two parts, A and B. Part A is a randomized, double-blind, parallel arm study to evaluate the safety and efficacy of LYT-100 compared to placebo in adults with post-acute COVID-19 respiratory complications. Part B is an Open Label Extension (OLE) study for patients who complete Part A.

NCT ID: NCT04650399 Completed - Chikungunya Clinical Trials

A Multicenter Study to Evaluate Safety and Immunogenicity of a Live-attenuated Chikungunya Vaccine in Adolescents

Start date: January 31, 2022
Phase: Phase 3
Study type: Interventional

This is a prospective, randomized, double-blinded, multicenter, pivotal study evaluating the final dose of VLA1553 (1 x10E4 TCID50 per dose) in comparison to a placebo control. The final dose of VLA1553 or control will be administered as single immunization on Day 1. Overall, approximately 750 male and female subjects aged 12 years to <18 years will be enrolled into the study.

NCT ID: NCT04649892 Not yet recruiting - Gaming Disorder Clinical Trials

Predicting Response to Naltrexone With Eye Tracking in Videogame Disorder

Start date: January 2021
Phase: Phase 2
Study type: Interventional

It is a double blind controlled study to test the hypothesis that it's possible to predict the response to naltrexone in Videogame Disorder with the use of Eye Tracking device, during a period of 12 weeks

NCT ID: NCT04649827 Recruiting - COVID-19 Clinical Trials

A Clinical Trial for Hospitalized Patients With COVID-19 in Ceará: ResCOVID Study

ResCOVID
Start date: April 2, 2020
Phase:
Study type: Observational

This is a case series of patients with COVID-19 admitted to the northeast Brazil region, in a referenced hospital for COVID-19, during the 2020 COVID-19 pandemic. Data will be collected prospectively and retrospectively. The main objective is to describe the characteristics of critically ill patients with COVID-19 and their clinical outcomes, and to identify risk factors associated with survival, to guide the strategy to mitigate the epidemic, both within each hospital and ICU and in public health management.

NCT ID: NCT04649619 Recruiting - Obesity Clinical Trials

Roux-en-Y Gastric Bypass: Clinical Trial

ERAPT
Start date: January 18, 2020
Phase: N/A
Study type: Interventional

The present study aims to describe the results of a modified gastric bypass surgery to ensure endoscopic access to the excluded remaining stomach, as well as to monitor the clinical conditions of comorbidities and the patient's quality of life, since associated complications can be found to the excluded stomach, such as: bile reflux, gastritis and / or gastric and duodenal ulcer, H. pylori infection, bleeding, gastric polyps and the possibility of gastric cancer in patients undergoing RYGB (Roux-en-Y gastric bypass), with one of the probable factors being the occurrence reflux of the duodenal content into the excluded portion of the stomach. In this sense, based on technical concepts of an established surgical procedure, the RYGB, the present project is not a proposal for a new procedure, but an adaptation of an existing technique. The proposal of the present study is about adaptations in RYGB surgery, which will enable endoscopic access to the remaining stomach, through the creation of a gastric communication.

NCT ID: NCT04648579 Completed - Clinical trials for Inpatient Facililty Diagnoses

Automated Documentation of Vital Parameters Using Mobile Stations and Activation of the Rapid Response Team

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

The documentation of vital signs is traditionally performed manually when the patient is not admitted in intensive care units, which can lead to documentary errors, long time for data acquisition and, consequently, impairment in the early identification of possible clinical deterioration. In-bed technology solutions are available to automate the collection of vital data and transfer information to a medical record or central electronic monitoring and its role in the health value chain needs further investigation. The investigators propose to evaluate the impact of the Connex Spot Monitor solution Welch Allyn (CSM / Hillrom) in conjunction with the Hillrom Connecta solution in a real world situation, conducting a cluster randomized trilal in wards of a tertiary hospital. In addition, this study aims to estimate the clinical effectiveness of a technological solution that performs an analysis of vital signs and automatically activates the rapid response team (RRT) when the pre-defined criteria are met, comparing it with the traditional manual method. The primary outcome is the number of times that the RRT fires in a timely manner.

NCT ID: NCT04648384 Completed - Sports Nutrition Clinical Trials

Acute Whey Protein And Casein Supplementation: Effect On Protein Metabolism After Resistance Exercise

Start date: March 20, 2016
Phase: N/A
Study type: Interventional

The proteins of human breast milk are the most important endocrine signaling system that promotes neonatal growth by increasing the release of insulin, insulin-like growth factor-1 (IGF-1), and the leucine-mediated mammalian target of rapamycin complex 1- (mTORC1) signaling of pancreatic β-cells. Remarkably, the branched-chain amino acids (BCAAs) leucine, isoleucine, and valine are involved in the growth-promoting effects of milk, protein biosynthesis, and metabolism because they physiologically stimulate insulin secretion The present study sought to investigate the effects of the combination of whey protein and casein in the ratio of 80:20 ("whey protein: casein" or "casein: whey protein") as breast milk proportion on the peak and the period of the permanence of branched-chain amino acids in the blood circulation, final metabolites of protein metabolism and delayed onset muscle soreness (DOMS) after a single bout of fasting or a resistance exercise session.

NCT ID: NCT04647994 Recruiting - Covid19 Clinical Trials

Exploratory Study: COVID-19 and Pregnancy

Start date: April 11, 2020
Phase:
Study type: Observational

The SARS-CoV-2 infection may behave differently in pregnant and postpartum women in the short and long term. Several risk factors or medication use can interfere on disease' evolution and vertical transmission. Thus, due the current pandemic and the scarcity of scientific studies involving pregnant women with covid-19 or positive serology, combined with the need to elucidate the behavior of this viral infection in pregnant women in our population, this study aims to evaluate the clinical and laboratory evolution, transplacental passage, gestational and neonatal outcomes in pregnancies with positive SARS-CoV-2.

NCT ID: NCT04647435 Recruiting - Postsurgical Pain Clinical Trials

Efficacy and Safety of APSCTC for the Treatment of Postsurgical Pain Due to Third Molar Extraction

CARLOTA
Start date: May 13, 2023
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of APSCTC compared to two active drugs in acute pain relief.