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Strabismus clinical trials

View clinical trials related to Strabismus.

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NCT ID: NCT03895632 Completed - Strabismus Clinical Trials

Eye Muscle Needle Electromyogram (EMu) Study

EMu
Start date: February 20, 2019
Phase:
Study type: Observational

In some cases, strabismus, or squint, is treated with injections of Botulinum toxin (BTX) to temporarily relax the eye muscle responsible for causing the eye to be pulled to one side. Due to the deep location of the muscles, electromyogram (EMG) needle guidance is used to help ensure the toxin is delivered accurately. EMG needle guidance involves listening to the EMG signal from the tip of the delivery needle - when the needle is in the right place a sound akin to "rain on a tin roof" is heard and the BTX can be injected. From previous research, clearly clinicians want to improve the technology of this procedure and increase the treatment efficacy and repeatability. After all, the current procedure is imprecise and subjective for what is a small target, with the eye muscles being around 2.5 mm to 4.7 mm in diameter. There may also be an increase in the likelihood of side effects such as droopy eyelids when the toxin spreads beyond the target muscle. There is a strong need for new knowledge to improve EMG needle guidance in this context. It is hypothesised that the EMG signal could be cleaned and mined for information in real time during the procedure, thus providing the clinician with better information to guide the positioning of the needle before injecting. This pilot study will deliver the knowledge essential to indicate the feasibility of doing this. If feasible, this study will inform a full study with the aim of benefitting patients by allowing new technology to be developed to improve the treatment of strabismus with BTX.

NCT ID: NCT03807011 Completed - Emergence Agitation Clinical Trials

Emergence Agitation in Pediatric Strabismus Surgery

Start date: July 7, 2017
Phase: N/A
Study type: Interventional

This study was performed to assess the effects of continuous remifentanil infusion and single bolus administration of fentanyl on the incidence of emergence agitation in pediatrics undergoing strabismus surgery.

NCT ID: NCT03806400 Completed - Strabismus Clinical Trials

Postoperative Nausea and Vomit in Strabismus Surgery

PONVISS
Start date: December 27, 2018
Phase:
Study type: Observational

Postoperative nausea and vomiting (PONV) is a major concern in paediatric inpatient surgery and may increase patient discomfort, delay patient discharge, and increase the cost of patient care. The incidence of PONV after strabismus surgery is relatively high, compared with other inpatient surgeries, particularly in children. Oculocardiac reflex (OCR) is a phenomenon defined by bradycardia or dysrhythmia during strabismus surgery. Oculocardiac reflex is commonly caused by the traction on the extraocular muscle (EOM), which, through the ophthalmic branch of trigeminal nerve, stimulates the vagal center. The afferent arm of the reflex is the ophthalmic branch of the trigeminal nerve, and the efferent arm is the vagus nerve, which diminishes sinoatrial node impulses and leads to bradycardia.While there is a general consensus regarding the role of unmodifiable risk factors for PONV, including the number of muscle and the occurrence of Oculocardiac reflex or not, the role of modifiable risk factors, such as duration of surgery and anesthesia and perioperatively administered medications, is still disputed. In the present study, the investigators evaluated whether these factors may be associated with postoperative nausea and vomiting after paediatric strabismus surgery while controlling for a range of covariates.

NCT ID: NCT03806270 Completed - Strabismus Clinical Trials

Hydroxyzine Dihydrochloride Premedication is a Necessity for Strabismus Surgery

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

Oculocardiac reflex (OCR) is usually happening in pediatric strabismus surgery and observed just when the surgent pulls the ocular muscles. The reflex is one of the trigemino-vagal reflexes, and causes bradycardia, arrhythmia, and even cardiac arrest during eye surgery. Premedication for relaxation with drugs like hydroxyzine dihydrochloride or midazolam before surgery of the pediatric population is often used in Turkey, although it is not recommended in foreign countries. Some recent studies showed that when midazolam and hydroxyzine dihydrochloride used together not only, they lessen agitation before surgery but also they prevent emergence agitation. The primary aim of this prospective observational study is to show the effect of hydroxyzine dihydrochloride on preventing the pediatric patient from Oculocardiac reflex related to strabismus surgery.

NCT ID: NCT03779282 Completed - Strabismus Clinical Trials

KETODEX for Emergence Delirium in Children Undergoing Outpatient Strabismus Surgery

Start date: February 15, 2018
Phase:
Study type: Observational

Strabismus surgery for children is a very common procedure, with a high incidence of emergence delerium in the recovery room. A combination of intravenous ketamine/dexmedetomidine, or ketodex, has been previously shown to reduce emergence delerium in children undergoing adenotonsillectomy. Here, we study its application in strabismus surgery.

NCT ID: NCT03778372 Completed - Strabismus Clinical Trials

Methadone for Emergence Delirium in Children Undergoing Outpatient Strabismus Surgery

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

Strabismus surgery for children is a very common procedure, with a high incidence of emergence delirium in the recovery room. Pain is often implicated in delirium. The primary aim of this study is to determine whether a single, intraoperative dose of methadone for outpatient ambulatory pediatric strabismus surgery reduces postoperative delirium.

NCT ID: NCT03713268 Recruiting - Healthy Clinical Trials

Intraoperative OCT Guidance of Intraocular Surgery II

MIOCT
Start date: September 30, 2018
Phase:
Study type: Observational

The overall five-year goals of the project are to develop novel technology to provide actionable new information through provision of live volumetric imaging during surgery, improving surgical practice and outcomes. The investigators believe this technology will enable novel ophthalmic and other microsurgeries not possible due to current limitations in surgical visualization.

NCT ID: NCT03672435 Completed - Pain Clinical Trials

Strabismus Recovery With Proparacaine and Oculocardiac Reflex

OCRprop
Start date: July 29, 2010
Phase:
Study type: Observational [Patient Registry]

Observational study to determine if topical anesthetic and intraoperative oculocardiac reflex influence post strabismus surgery recovery.

NCT ID: NCT03668067 Completed - Refractive Errors Clinical Trials

Performance of 2WIN Photoscreener With Corneal Reflex Compared to School Bus Retinoscopy by AAPOS Guidelines

2WINbus
Start date: April 2, 2018
Phase:
Study type: Observational [Patient Registry]

Pediatric eye patients receive infrared photoscreener screening and skiascopy as a part of routine examination to compare ability to detect amblyopia risk factors.

NCT ID: NCT03663413 Completed - Bradycardia Clinical Trials

Oculocardiac Reflex Brain Wave Monitor

OCRBIS
Start date: August 27, 2009
Phase:
Study type: Observational

Oculocardiac reflex during routine strabismus surgery was prospectively observed in association with routine brain wave monitoring. Providence Hospital institutional review board (IRB) approved this observational study without need for consent.