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Diplopia clinical trials

View clinical trials related to Diplopia.

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NCT ID: NCT04957745 Completed - Diplopia Clinical Trials

Understanding Visual Confusion Using Stereoscopic Displays

Start date: November 9, 2021
Phase: N/A
Study type: Interventional

In this research study we want to test how people understand a visual scene when the same image is presented to both the eyes, but portions of these images are altered in terms of contrast, depth or in some cases motion.

NCT ID: NCT03660852 Completed - Stroke Clinical Trials

Impact of a Magnetic Resonance Imaging (MRI) Scanner Exclusively Dedicated to Emergency in the Clinical Management of Patients Presenting With Diplopia or Dizziness

IRM-DU
Start date: July 24, 2018
Phase:
Study type: Observational

IRM-DU is a prospective observational single center study conducted in an emergency department to evaluate the impact of a MRI scanner exclusively dedicated to emergency in the clinical management of patients presenting with dizziness or diplopia. The study will compare 2 strategies : after and before availability of a MRI scanner dedicated to emergency. The primary endpoint is the proportion of patients with a diagnosis of stroke confirmed by imaging (MRI or Computed tomography (CT)) in the group "before implementation of the emergency MRI scanner" and the group "after implementation of the emergency MRI scanner". The hypothesis is that the availability of a MRI scanner dedicated to emergency will improve the diagnosis of stroke in patients presenting with dizziness or diplopia, and will reduce Emergency Department stay, hospital stay and hospitalisation costs.

NCT ID: NCT02576925 Recruiting - Diplopia Clinical Trials

A Predictive Score for the Ischemic Etiology of a Transient Diplopia (VASCO-DIP)

VASCO-DIP
Start date: September 24, 2015
Phase:
Study type: Observational

The transient diplopias (TD) is defined by a short diplopia. Their etiology may be ophthalmological, neurological non-ischemic or of ischemic origin. The difficulty is to recognize an ischemic mechanism which imposes emergency cares. A clinical score could help the clinician to recognize the etiology of the TD .

NCT ID: NCT01119144 Recruiting - Fractures Clinical Trials

Polycaprolactone / Tricalcium Phosphate (PCL/TCP) v Titanium Orbital Implant : Randomised Trial

PCL/TCP
Start date: April 2010
Phase: Phase 2
Study type: Interventional

Hypothesis: Polycaprolactone / Tricalcium Phosphate Orbital (PCL / TCP) Implant is as effective in the reconstruction of the Orbital walls as Titanium Mesh implant. In this study we will be conducting a randomised trial to compare implants made of 2 materials for Orbital reconstruction - Polycaprolactone / Tricalcium Phosphate (PCL / TCP) - Titanium Patients to be recruited : - 80 randomised equally into the 2 groups - age range: 21 - 70 - includes orbital wall defects from trauma, after osteotomies - excludes patients with Diabetes Mellitus, known allergies to polycaprolactone & its analogues, know allergies to Tricalcium Phosphate & its analogues, infections generalised & around the orbital region Trial Duration: April 2010 - March 2015 Follow up: - postoperative 1 week, 1 month, 3 months, 6 months, and 12 months - Computer Tomographic (CT) scan of Orbits immediate postoperative and at 12 months appointment