Clinical Trials Logo

Other clinical trials

View clinical trials related to Other.

Filter by:

NCT ID: NCT04613427 Completed - Clinical trials for Intracranial Aneurysm

Predictors of Rupture Risk of Intracranial Aneurysms

RAPID
Start date: April 1, 2018
Phase:
Study type: Observational [Patient Registry]

Patients admitted to Haukeland University Hospital with either UIA or aSAH underwent a measurement of bioelectrical impedance and body mass composition using InBody 10. Lipids and lipoproteins were collected from plasma. 60 patients in total were included in the study.

NCT ID: NCT04613375 Completed - Clinical trials for Community Acquired Pneumonia (CAP)

PCV13 Effectiveness Study Against Hospitalised VT Pneumococcal CAP in Adults 60 Years and Older

Start date: March 12, 2021
Phase:
Study type: Observational

Low interventional, prospective, multicentre, hospital-based study involving adults 60 years of age and older hospitalised with CAP at participating sites.

NCT ID: NCT04613063 Completed - Cystic Fibrosis Clinical Trials

Proximal Intestinal Obstruction Syndrome (PIOS) in a Patient With Cystic Fibrosis: A New Syndrome

Start date: October 19, 2020
Phase:
Study type: Observational

A case of a patient with cystic fibrosis with bowel obstruction due to a proximal intestinal obstruction syndrome (PIOS) is presented.This syndrome can be diagnosed with the DIOS definition, with the only distinction of a more proximal location in the gastrointestinal tract, such as the stomach, the duodenum, or the jejunum.

NCT ID: NCT04612998 Completed - Obesity Clinical Trials

Combined Spinal Epidural Anesthesia in Obese Patients Undergoing Cesarean Surgery

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

This study investigated the maternal and fetal effects during performance of CSEA in the left lateral decubitus and sitting positions in obese pregnant women undergoing elective cesarean section.

NCT ID: NCT04612777 Completed - Bipolar Disorder Clinical Trials

A Trial of "Opening Doors to Recovery" for Persons With Serious Mental Illnesses

ODR
Start date: June 15, 2014
Phase: N/A
Study type: Interventional

Insufficient community-based support after inpatient discharge for persons with serious mental illnesses (SMI) may lead to re-hospitalization, excessive criminal justice involvement, homelessness, and an inability to embrace recovery. In fact, many of these especially vulnerable persons find themselves in a cycle of repeated hospital stays, arrests, and even homelessness, with little support for real recovery. Public mental health systems are struggling to address these problems. Evidence-based, comparatively inexpensive, time-limited community support models are needed to reduce institutional recidivism and facilitate recovery. The Georgia chapter of the National Alliance on Mental Illness (NAMI-GA) developed Opening Doors to Recovery (ODR), and we have collected extensive preliminary data on it. ODR is now being tested in a randomized controlled trial (RCT) taking place in southeast Georgia where ODR was first developed. The primary goals of ODR are to prevent institutional recidivism (i.e., going back into the hospital) and to promote recovery among persons with SMI like schizophrenia and bipolar disorder. The ODR intervention is comprised of several components that work together to address barriers to successful integration into the community among individuals with SMI and repeated inpatient hospitalizations. A team of 3 specially trained "Community Navigation Specialists" (CNSs, also called Navigators) provides intensive, mobile, community support to persons with SMI with a defined history of inpatient recidivism (i.e., repeated hospital stays). We are carrying out a fully powered trial of ODR in a 7-county catchment area in southeast Georgia, which is an ideal real-world location to carry out the study. During the 5-year study period, we will randomize 240 persons with SMI and a history of ≥2 inpatient stays in the past 12 months to ODR (n=120, followed for 12 months, with a maximum CNS caseload of 40) versus community care in traditional intensive case management or case management (ICM/CM, n=120). Assessments are conducted at baseline (just before hospital discharge), and at 4, 8, 12, and 18 months.

NCT ID: NCT04612543 Completed - Clinical trials for Dental Caries Extending Into Dentin

Clinical Evaluation of Extensive Direct Composite Restorations With Polyethylene Fiber

Start date: February 10, 2019
Phase: N/A
Study type: Interventional

The aim of this clinical trial was to compare the clinical performances of composite resin restorations with/without the polyethylene fiber to the first permanent molar teeth with extensively carious pediatric patients. A total of 75 restorations with (FC; n=38)or without (C; n=37) fiber were placed in the first permanent molar teeth. Restorations were evaluated at baseline-6-12-18 months according to the modified-USPHS criteria. Data were analyzed with Chi-Square and Cochran's Q (p<0.05).

NCT ID: NCT04612153 Completed - Clinical trials for Describe Musculoskeletal Disorders of Workers

Musculoskeletal Disorders of Workers in a Production and Distribution Company in Argentina

Start date: March 15, 2019
Phase:
Study type: Observational

Describe musculoskeletal disorders of workers in a company in Argentina regarding working areas and demographic carachteristics of the workers.

NCT ID: NCT04612101 Completed - Clinical trials for the Focus of the Clinical Trial is on the Brain Temperatures in Normal Human Subjects

Check Brain Temp Trial

Start date: October 1, 2018
Phase:
Study type: Observational

Despite some controversial results, many patients and animal studies have suggested significant benefit of using hypothermia treatment in stroke patient population. However, certain questions for how to applying this therapy properly such as when to start, what is the optimal temperature, how long is the duration, and what is the best hypothermia technology that may avoid the complications including focal soft tissue injuries are still remain questioned. In this study, we will utilize the linear relationship of temperature vs. chemical shift in MR Spectroscopy to measure the brain temperatures in normal men.

NCT ID: NCT04611386 Completed - Clinical trials for Contrast Agents and Oral Factor Xa Inhibitor

The Effect of Contrast Agents on the Anticoagulant Properties of Oral Factor Xa Inhibitors

Start date: January 1, 2019
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to evaluate the effect of iohexol as a contrast agent on the anticoagulant activity of oral factor Xa inhibitors.

NCT ID: NCT04611230 Completed - Clinical trials for Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2)

A Study to Assess Infection Rate of Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2) and It's Affect on Quality of Life in Adult Volunteers in Lake County, Illinois

CONTACT
Start date: November 5, 2020
Phase:
Study type: Observational

Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Lung failure is the main cause of death related to COVID-19 infection. The main objective of this study is to assess infection of SARS-CoV-2 and how quality of life is affected in adult volunteers in Lake County, Illinois. Volunteers will be recruited through digital advertisements and participants will be required to fill an online questionnaire. Upon consent, participants will be required to provide nasal swab and blood sample. Approximately 1250 adult volunteers living or working in Lake County, IL will be enrolled. Participants will be followed for approximately 9 months and will be required to provide nasal swab and blood samples every 3 months and complete questionnaires every 2 weeks. There may be higher treatment burden for participants in this trial. Participants will be monitored by medical assessments, blood tests and questionnaires.