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NCT ID: NCT04357899 Completed - Ischemic Stroke Clinical Trials

Stroke Research Consortium in Northern Bavaria (STAMINA)

STAMINA
Start date: January 1, 2006
Phase:
Study type: Observational

Each year, approximately 15 million people suffer a stroke worldwide of which 80% are due to ischemic cerebral infarction. Based on the results of randomized controlled trials, treatment options and patient outcomes in acute ischemic stroke have dramatically improved in recent years. However, these advances in thrombolysis and endovascular therapy need to be established outside controlled trials to optimize stroke management, treatment procedures, patient selection and inter-hospital transfer in clinical practice. This multicenter longitudinal cohort study is based on a large stroke care network in Northern Bavaria, Germany (region of more than 3.5 million inhabitants) to evaluate and improve treatment in ischemic stroke.

NCT ID: NCT04356040 Completed - Clinical trials for Paroxysmal Atrial Fibrillation

TactiFlex Paroxysmal Atrial Fibrillation IDE Trial

Start date: June 29, 2020
Phase: N/A
Study type: Interventional

Prospective non-randomized parallel-assignment multi-center clinical investigation. The study design includes two subject cohorts: 1) Paroxysmal Atrial Fibrillation Main Study, and 2) Paroxysmal Atrial Fibrillation High Standard Power Substudy. Subjects in the main study cohorts are to be treated using the full range of ablation power settings in the Instructions For Use. Subjects in the High Standard Power Substudy are to be treated in the upper end of the recommended ablation power settings (40-50 Watts).

NCT ID: NCT04354883 Completed - Cardiac Arrest Clinical Trials

The Schmitz-Hinkelbein Method. A New Technique for CPR in Space.

Start date: January 2, 2020
Phase: N/A
Study type: Interventional

The risk of a severe medical event during long-duration spaceflight is significant and can endanger both the whole mission and crew. There is a certain risk for a cardiac arrest in space requiring cardiopulmonary resuscitation (CPR). So far, 5 known techniques to perform CPR in microgravity have been reported. The aim of the present study was to describe and gather data for two new CPR techniques useful in microgravity.

NCT ID: NCT04353817 Completed - Cystic Fibrosis Clinical Trials

A Study Evaluating Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Subjects 6 Through 11 Years of Age With Cystic Fibrosis and F/MF Genotypes

Start date: June 19, 2020
Phase: Phase 3
Study type: Interventional

This study will evaluate the efficacy and safety of elexacaftor (ELX) / tezacaftor (TEZ) / ivacaftor (IVA) triple combination (TC) in subjects 6 through 11 years of age with cystic fibrosis (CF) who are heterozygous for F508del and a minimal function (MF) mutation (F/MF genotypes).

NCT ID: NCT04353596 Completed - COVID-19 Clinical Trials

Stopping ACE-inhibitors in COVID-19

ACEI-COVID
Start date: April 20, 2020
Phase: Phase 4
Study type: Interventional

ACEI-COVID-19 is a multicenter, randomized trial testing the hypothesis that stopping/replacing chronic treatment with ACE-inhibitors (ACEI) or angiotensin receptor blockers (ARB) improves outcomes in symptomatic SARS-CoV2-infected patients

NCT ID: NCT04352452 Completed - Clinical trials for Excessive Musculoskeletal Stress

Save Our Surgeons - Differences in Stress of Robot-assisted Laparoscopic Surgery vs. Conventional Laparoscopic Surgery

SOSII
Start date: June 1, 2019
Phase:
Study type: Observational

Monocentric trial to evaluate differences in musculoskeletal and cognitive stress of robot-assisted laparoscopic surgery (RALS) vs. conventional laparoscopic surgery (CLS). Demographic and personal data are collected and pseudonymized as well as video recordings are performed during surgery. Simultaneously, surface electromyography (EMG) and electrocardiography (ECG), motion tracking data are collected. Additionally, saliva cortisol, perceived discomfort and mental load will be assessed within certain time intervals. The surgeon is not disturbed in his activity and movement by the equipment. Afterwards, the surgeon will be interviewed in a 15-minute standardized interview about the surgery process and the subjective stress sensitivity. Only routine interventions will be recorded, in case of unforeseen complications, the recording will be stopped immediately

NCT ID: NCT04351854 Completed - Clinical trials for Corona Virus Infection

Registry for Clinical Presentation and Management of Patients With COVID-19 in the Emergency Room

ReCovER
Start date: April 20, 2020
Phase:
Study type: Observational

Patients with COVID-19 usually present in the ED and receive their initial medical check-up here. We will try to gather information of comorbidities and other conditions at the time of presentation of COVID-19 patients to the ED. The course of the disease prior to admission as well as the momentary health status at presentation to the ED are of interest because they influence risk stratification and decision-making of treating physicians. The ratio of patients with mild or moderate to severe symptoms will help to calculate the need for hospital beds including beds on Intensive Care Units (ICU) and Intermediate Care Units (IMC), as well as the need for other hospital resources.

NCT ID: NCT04349813 Completed - Transfusion Clinical Trials

Perioperative Pediatric Blood Transfusion Therapy

Start date: April 15, 2020
Phase:
Study type: Observational

The present retrospective study analyses perioperative haemotherapy in children and adolescents at the University Hospital Frankfurt.

NCT ID: NCT04347824 Completed - Covid-19 Clinical Trials

Predict Adverse Events by Covid-19 Nephritis

Start date: April 27, 2020
Phase:
Study type: Observational

This non-interventional, observational study retrospectively (and in parts prospectively) investigates, if a Covid-19 associated Nephritis, diagnosed by Urine-dipstick and further Urine-analyses on addmission, can help to predict later complications, adverse outcomes and later need for ICU-capacity in Covid-19 patients as well as can guide preventive strategies.

NCT ID: NCT04347564 Completed - Vision Disorders Clinical Trials

Usability of the Software MacuFix for the Categorization of Metamorphopsia

MacuFix
Start date: May 4, 2020
Phase:
Study type: Observational

The usability of a novel test to categorize a distorted visual impression (metamorphopsia) is examined with the questionnaire "SUS"