Effect of Neuromuscular Blockade on the Oculomotor by Not Squinting Child
STRABO
2 other identifiers
observational
60
1 country
2
Brief Summary
Strabismus is a common condition (4-6% of the population) . The screening and treatment is a public health issue. Indeed, beyond the disfigurement, this disease is very supplier of amblyopia which is definitive if it is not detected and treated early (before 6 years old). Initial treatment of strabismus is medical with orthoptic reeducation through penalization of the better eye in case of amblyopia or wearing optical correction in case of associated refractive disorder. The second step is the treatment of strabismus is the surgery, when medical treatment has not resulted in a recovery of the visual axes. The principle of surgery is to weaken or strengthen one or more extraocular muscles of one (or two) eye to correct the eyes squint deviation. The main difficulty of surgical treatment is to assess the amount of strengthening or weakening muscles to do in order to obtain the best result and for a long time. The investigators know that the postmortem anatomical position of the eyes is generally a slight elevation and divergence, but is inferior to the angle of divergence of the orbital axes. Curare and similar products which inhibit the nervous transmission at the neuromuscular junction, can be used to reproduce this situation in normal subjects. The sign of general anesthesia is then to evaluate the angle of strabismus when the patient is under deep general anesthesia and with a complete muscle relaxation, obtained only when curarised it. If one or both eyes are recovering under general anesthesia, strabismus is mainly due to dynamic changes and surgery limiting muscle play (wire operation) and sometimes one eye is justified. A combination of both is possible (down + wireless), guided by the importance of the sign of general anesthesia on two prominent eyes or one eye. This sign of general anesthesia is however less known and most poorly quantified in healthy subjects. Yet it seems very important to determine what is deviation in normal subjects after neuromuscular blockade, as his eye movement is also subject to mechanical factors and spastic. This would indicate whether the state of rectitude (no strabismus) is the result of a deviation at complete rest (appearing under general anesthesia) and corrected by spastic elements wakefulness or, in another case this righteousness is already present in the state of general anesthesia (due to static factors) and slightly modified by enlightenment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Nov 2010
Longer than P75 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2010
CompletedFirst Submitted
Initial submission to the registry
February 3, 2015
CompletedFirst Posted
Study publicly available on registry
February 11, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2016
CompletedJanuary 25, 2017
January 1, 2017
6.1 years
February 3, 2015
January 24, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Horizontal deflection of the two eyes under deep general anesthesia and under curare
When the patient is under deep general anesthesia (Bispectral Index (BIS) \< 50) ,one photo is taken. A seconde one is taken after curare induction.
From the anesthesia to the end of the surgery
Secondary Outcomes (1)
Horizontal deflection of the two eyes under deep general anesthesia
From the anesthesia to the end of the surgery
Study Arms (1)
healthy subjects waiting for surgery
patients for whom surgery under general anesthesia with administration of curare is planned will be offered an examination of the eyes before and during surgery
Interventions
Before planed surgery, an ophthalmologist measures the patient's visual acuity and realise an oculomotor examination. Measurement the refraction and the axial length of the eye is performed. Photographs wakefulness are performed. During surgery, participation in this study does not involve any change in the course of anesthesia and surgery. Pictures of the eye will be performed under general anesthesia. Timing photos will be dictated by the values of BIS and train-of-four (TOF). Photos will be conducted at different times, with the "top" given by the anesthetist under the following conditions: Deep anesthesia: BIS \<50 Deep anesthesia and muscle relaxation: BIS \<50 and TOF 0/4
Eligibility Criteria
Patients for whom surgery under general anesthesia with administration of curare is planned
You may qualify if:
- normal visual acuity for age: 10/10 (Test of Cadet) Rossano 2 for 4-6 years old. 10/10 (scale Monoyer) Parnaud 1.5 for 7-15 years old.
- normal oculomotor examination: Examination under normal alternating display eliminating strabismus
- Binocular vision less than or equal to 60 sec/arc for the stereoscopic vision test
- Refraction WITHOUT cycloplegia within normal limits: below 2 dioptries myopia, hyperopia less than 1.5d, below 1 dioptry astigmatism, anisometropia less than 1 dioptry.
- Examination of the fundus without normal pupillary dilation
- Axial length 6 normal for age as measured by noncontact biometer to eliminate refractive offset anomaly axial length by abnormal
You may not qualify if:
- presence of anterior eye history
- children whose behavior suggests a poor cooperation when taking photo awakeness
- children with abnormal limb
- scheduled surgery without the use of curare
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Centre Hospitalier Universitaire de Saint Etienne
Saint-Étienne-de-Montluc, Pays de la Loire Region, 69003, France
CHU de Nantes
Nantes, 44000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Pierre PM MANOLI, M.D
Centre Hospitalier Universitaire de Saint Etienne
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 3, 2015
First Posted
February 11, 2015
Study Start
November 1, 2010
Primary Completion
December 1, 2016
Study Completion
December 1, 2016
Last Updated
January 25, 2017
Record last verified: 2017-01
Data Sharing
- IPD Sharing
- Will not share