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NCT ID: NCT04185857 Completed - Clinical trials for Primary Aldosteronism Due to Aldosterone Producing Adenoma

MRA and ARB Treatment in Screening of Primary Aldosteronism

EMIRA
Start date: January 1, 2018
Phase:
Study type: Observational

Current guidelines recommend withdrawal of treatments that affect the aldosterone/renin ratio (ARR) when screening for primary aldosteronism (PA). However, abandonment of mineralocorti-coid-receptor antagonist (MRA) and/or blockers of the renin-angiotensin system can deteriorate control of blood pressure (BP) and hypokalemia. Thus, in consecutive patients with an unambiguous diagnosis of PA in wash-out from confounding treatments and subtyped by AVS, the investigators have compared within-patient the plasma aldosterone and active renin concentration, and the ARR values, measured at baseline, and after a one-month treatment with MRA alone and combined with an AT-1 receptor blocker (ARB). Patients on a regular salt intake have been treated with canrenone (50-100 mg orally) for 1 month, after which olmesartan (10 or 20 mg orally) has been added for another month with up-titration of both treatments over the first 2 weeks to control BP and hypokalemia, however maintaining background therapy. The biochemical variables and the ARR have been assessed in an identical manner at baseline values and after each month of treatment. The investigators calculated that with a sample size of 40 patients the study will have a 95% power to show a clinically significant 20% change in the ARR at an 5% alfa-value using a two-sided paired t-test. Hence, this study will allow to determine if an MRA alone, or added to an ARB at doses that control BP and hypokalemia, affect or not the ARR, thus allow to establish if these agents can be administered or must be forbidden during the screening of PA.

NCT ID: NCT04185324 Completed - Clinical trials for Typical Preschoolers Who Can Not Zipper

Efficacy of an Intervention to Teach Zippering: A Two-Group Control Study

Start date: September 1, 2019
Phase: N/A
Study type: Interventional

Preschoolers are assigned to a control group or a comparison group to examine the efficacy of a new intervention to teach the skill of engaging and pulling up a zipper.

NCT ID: NCT04185298 Completed - Clinical trials for Amnestic Mild Cognitive Impairment

mSIM: Mobile Simultaneous Aerobic Exercise and Memory Training Intervention for Amnestic Mild Cognitive Impairment

mSIM
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

The mSIM study involves developing and conducting feasibility testing of a web-based application that will deliver mobile-based simultaneous exercise and memory skills training program (mSIM) for amnesic Mild Cognitive Impairment (aMCI) patients. The randomized control trial (RCT) will evaluate the efficacy of mSIM on memory performance and everyday functioning using 2 study arms (Group 1 activity monitoring control (via Fitbit) (CON) vs Group 2 mSIM intervention plus activity monitoring via Fitbit). mSIM treatment response will be evaluated using neuropsychological and functional evaluation. Concentration levels of peripheral biomarkers Brain-derived neurotrophic factor (BDNF) and norepinephrine (NE) also be assessed.

NCT ID: NCT04184674 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Impact of the Transpulmonary Pressure on Right Ventricle Function in Acute Respiratory Distress Syndrome

VD-SDRA
Start date: June 11, 2020
Phase: N/A
Study type: Interventional

Pulmonary distension induced by mechanical ventilation physiologically alters right ventricle pre and after-load, hence might lead to right ventricle failure. The hypothesis is that in Acute Respiratory Distress Syndrome, the occurence of a right ventricle failure under lung protective ventilation might : i) be correlated to the transpulmonary pressure level, ii) lead to global heart failure, iii) and extremely result in poor outcome and death. The primary objective is to test the impact of transpulmonary pressure on right ventricular function in Acute Respiratory Distress Syndrome in adults and children. Secondary objectives are : i) to compare thresholds of transpulmonary pressure associated with right ventricle failure between children and adults. ii) to assess if there is an association between transpulmonary pressure and morbidity and mortality. - For pediatric patients, a specific monitoring with electrical impedance tomography (EIT) will allow: - To assess if the transpulmonary pressure is associated with the level of regional pulmonary overdistention (or collapse) on electrical impedance tomography.(EIT) - To assess if there is an association between the occurrence of right ventricular failure, and distribution of ventilation on EIT.

NCT ID: NCT04184427 Completed - Clinical trials for Varying Heights of Power Arm During en Masse Retraction

Effects on Maxillary Anterior Dentition Following En Masse Retraction Using Mini-implants and Various Heights of Anterior Power Arm.

Start date: June 25, 2019
Phase: N/A
Study type: Interventional

The controlled three dimensional movement of anterior dentition during orthodontic treatment is a desire of every orthodontist. Maxillary en masse retraction with mini implants has been reported to provide absolute anchorage thus utilizing the complete extraction spaces thereby enhancing patient's esthetics. Power arm or anterior retraction hook permits the application of force close to a desired direction thereby warranting better anterior dentition control. Various heights of power arms and proposed centre of resistance for six maxillary anterior teeth have been estimated through finite element model and also from a very limited number of clinical studies. For a set of teeth, the determination of centre of resistance is complex in actual clinical scenario and response of force applied from certain level for better anterior dentition control requires sufficient clinical evidence suggestive of further clinical studies to endow orthodontists to hasten treatment due to less time consumption during finishing stage of orthodontic treatment.

NCT ID: NCT04184401 Completed - Clinical trials for Living Donor Liver Transplantation

Effect of Ascites Replacement Strategy on Time to 1st Flatus After LDLT

Start date: January 1, 2020
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate difference in the rate of recovery of intestinal motility according to different ascites replacement strategy after living donor liver transplantation.

NCT ID: NCT04184297 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Comparative Effectiveness and Safety of Tiotropium and Olodaterol in Comparison to Triple Therapy

Start date: November 1, 2019
Phase:
Study type: Observational

To assess the comparative effectiveness of combination Tiotropium and Olodaterol (Tio+Olo) (FDC) compared to combination LAMA/LABA and ICS (fixed or open), and to explore whether this varies across COPD sub populations defined by exacerbation risk

NCT ID: NCT04183972 Completed - Clinical trials for Ultrasound Therapy; Complications

Identification of Interscalene Brachial Plexus on Ultrasonography Using a Deep Neural Network

IBRUNNET
Start date: December 1, 2019
Phase: N/A
Study type: Interventional

The purpose of the study is to develop and validate an algorithm based on deep neural networks (DNNs) to identify interscalene brachial plexus on ultrasonography automatically.

NCT ID: NCT04183881 Completed - Psoriatic Arthritis Clinical Trials

A Phase 4 Clinical Study of Brodalumab

Start date: July 4, 2016
Phase: Phase 4
Study type: Interventional

This study [4827-005 (post market)] is designed to evaluate the safety and efficacy of long-term exposure to brodalumab in subjects with plaque psoriasis (psoriasis vulgaris, psoriatic arthritis) who have completed Study 4827-003 (Study 003) and in subjects with pustular psoriasis (generalized) or psoriatic erythroderma who have completed the Study 4827-004 (Study 004). 4827-005 study was conducted as phase 3 clinical trial until July 4th 2016 (approval date in Japan). After that date 4827-005 study was switched to phase 4 study.

NCT ID: NCT04183140 Completed - Clinical trials for ST Elevated Myocardial Infarction

Comparison of Radial and Ulnar Artery Intervention in Patients With ST Elevated Myocardial Infarction

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

In the literature, there are no studies comparing these two pathways in ST elevation myocardial infarction (STEMI). In this patient group, it will be investigated whether transulnar intervention causes similar or less complications than transradial intervention, and whether it provides superiority or similarity in terms of outcomes.