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NCT ID: NCT04833166 Completed - Clinical trials for Intubation; Difficult or Failed

Comparing Full vs. Partial Glottis View Using CMAC D-Blade Video Laryngoscope in Simulated Cervical Injury Patient

Start date: May 25, 2021
Phase: N/A
Study type: Interventional

Direct laryngoscope requires proper alignment of the oro-pharyngeal-laryngeal axis to provide an optimal glottic view for intubation. However, in cervical spine patients, this alignment is not possible thus resulting in an increased risk of fail intubations. D-blade comes with an elliptically tapered blade shape rising at the distal end to provide better glottic visualization in comparison with direct laryngoscopes. Hence, CMAC D-blade is preferred in simulated cervical spine injury where intubator needs to maintain a neutral neck position. However, intubation time may be significantly longer due to difficulty in negotiating the endotracheal tube pass vocal cord and impingement of endotracheal tube to the anterior wall of trachea. There is a study published Glidescope which is also a hyperangulated videolaryngoscope suggested that obtaining a partial glottic view of larynx may facilitate a faster and easier tracheal intubation when compare to a full glottis view. The aim of this study is to clinically evaluate the time of tracheal intubation in relation to the full glottic view vs. partial glottic view which is deliberately obtained when using CMAC D-blade video laryngoscopy in simulated cervical spine injury.

NCT ID: NCT04832737 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Strength-based Treatment Approach for Adults With ADHD

Start date: September 6, 2021
Phase: N/A
Study type: Interventional

The aim of the research is to develop a treatment program with positive self-awareness and self-determination outcomes for adults with Attention Deficit Hyperactivity Disorder (ADHD). Current treatments are based in a characterisation of ADHD oriented on deficits impairing everyday functioning, with primary goals of symptom control and reduction. However, treatment approaches are not standardised and only evidence short-term effectiveness. This project proposes an alternative approach to understanding ADHD behaviours, supported by Self Determination Theory (SDT). Research shows SDT based treatment approaches can support engagement of intrinsic motivation and longterm integration of behavioural change. ADHD research shows individuals are impaired in some contexts but not in others and can manage well, indicating potential for ADHD neurodiverse "strengths" which could be developed and supported. Recent psychology research recommends cultivating positive psychological factors and emotions to improve mental health and wellbeing. Adults aged 18+ with a confirmed ADHD diagnosis will be invited to participate in two projects: Intensive online interviews of 1 hour will be conducted to identify, explore, and construct a theory about the factors, or "natural strengths" in lived experience of ADHD that help individuals to overcome everyday impairments. These factors will be incorporated into a pilot feasibility study of an SDT based 12-week treatment programme focusing on understanding the lived experience of ADHD and building on these strengths. The treatment will be designed for individual participants and delivered online. This study will have two sets of participants: one group will go directly to treatment, the other will go on a 12-week waiting list to create a comparison group. The second group will then be offered the 12-week treatment. Measures of experience of the participants will be looking for the feasibility, acceptability and efficacy of this treatment, as well as indicators of symptom improvement, and changes in self-awareness and self-regulation skills.

NCT ID: NCT04832724 Completed - Clinical trials for Neovascular Age-related Macular Degeneration

RGX-314 Gene Therapy Pharmacodynamic Study for Neovascular Age-related Macular Degeneration (nAMD)

Start date: February 22, 2021
Phase: Phase 2
Study type: Interventional

RGX-314 is being developed as a novel one-time gene therapy for the treatment of neovascular (wet) age-related macular degeneration (nAMD) also referred to as Wet AMD. Wet AMD is characterized by loss of vision due to new, leaky blood vessel formation in the retina. The purpose of this phase 2, open label study is to evaluate whether different doses of RGX-314 from two different formulations (clinical versus eventual commercial formulation) perform the same in humans when delivered by subretinal administration

NCT ID: NCT04832672 Completed - Clinical trials for The Optimal Sequence of Radiotherapy and Systematic Tyrosine Kinase Inhibitors in Treating Brain Metastases

Sequence of Radiation and Targeted Therapy in Brain Metastases

Start date: October 1, 2010
Phase:
Study type: Observational

The investigators conducted a single institutional, retrospective cohort study to demonstrate the appropriate treatment strategy of upfront intracranial radiotherapy or upfront targeted therapy in patients with brain metastases, including an assessment of its feasibility and toxicity.

NCT ID: NCT04832633 Completed - Radiation Exposure Clinical Trials

The Best Parameters for Imaging Agent Injection and Scanning Methods in Computed Tomography Angiography

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

Background: The contrast time-enhancement profiles of pulmonary artery (PA) and the aorta differ by using computed tomography (CT) angiography. Our purpose is to identify the optimal CT protocol for assessment of both vessels in one-time CT scan. Methods: The investigators prospectively enrolled 101 cases of CT angiography with suspicion of pulmonary embolism or aortic dissection in our center from 2018 to 2020. Forty cases receiving traditional two-time CT scans were collected retrospectively from 2015 to 2018. The investigators designed four groups: test bolus (TB) I, II and bolus-tracking (BT) I, II. The enhancement of the both vessels and the radiation dose of these four groups were collected. Traditional group was separated into traditional PA scan and traditional aorta scan. Data analyzed among the BT groups and the traditional groups were performed.

NCT ID: NCT04832581 Completed - Clinical trials for Urinary Tract Infection During Pregnancy

Developing Self-care Behaviors for Urinary Tract Infections

Start date: January 20, 2020
Phase: N/A
Study type: Interventional

The research was designed in a randomized controlled quasi-experimental type in order to reveal the effect of "Self-Care Behaviors Development Program for Urinary Tract Infections" prepared according to Orem's Self Care Model on the behavioral change in pregnant women.

NCT ID: NCT04832399 Completed - Clinical trials for Relapsing Remitting Multiple Sclerosis

Study of Tysabri in Early Relapsing Remitting Multiple Sclerosis Participants

TYPIFI
Start date: November 12, 2013
Phase:
Study type: Observational

The purpose of this study is to evaluate the impact of an early treatment with Natalizumab on the management of the progressive nature of Relapsing Remitting Multiple Sclerosis (RRMS).

NCT ID: NCT04831268 Completed - Appetitive Behavior Clinical Trials

Effects of Traditional Greek Meals on Glycemic Responses

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

This study investigated the effects of Greek traditional meals in dehydrated form consumed after reconstitution with water on glycemic responses

NCT ID: NCT04831177 Completed - Clinical trials for Myopic LASIK Candidates With Spherical Equivalent up to - 10 Diopters

Thin-Flap Laser in Situ Keratomileusis Associated Dry Eye

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

Laser in situ keratomileusis (LASIK) eye surgery continues to be the most common refractive procedure used to correct different forms of ametropia. Although the introduction of femtosecond technology has markedly reduced the incidence of intraoperative flap complications and allowed a better control on flap parameters, dry eye remains one of the most challenging postoperative complications.

NCT ID: NCT04830917 Completed - Clinical trials for Conservatively Treated Mallet Finger Injury

Conservative Treatment of Mallet Finger Injury

Start date: April 24, 2017
Phase: N/A
Study type: Interventional

Comparing outcomes of individuals treated with Kinesiotape and oval 8 versus quick cast for a conservatively managed mallet finger injury. Outcomes include DIP joint extension lag, patient satisfaction and function via the MHQ.