Ptosis Clinical Trial
Official title:
Quantitative Evaluation of Levator Palpebra Muscle Strength
The purpose of this study is to assess a new technique of measurement for the levator
muscle.
this measurement may be applied during a clinical evaluation of eyelid malposition.
our purpose is to quantify the levator muscle strength and to corelate it to standard
levator muscle strength assessment techniques routinley used in the oculoplastic clinic.
This study will include patients refered to our oculoplastic department for evaluation of
eyelid disorders (ptosis or eyelid malpositions due to various mechanical, muscular,
neurogenic factors).
all patients will be over 21 years old, with eligibility for signing an informed concent
form.
all patients will undergo a full clinical standard evaluation of eyelid malposition made as
part of the routine evaluation of eyelid malpositions. as part of this evaluation- the
levator muscles strength will be measured by monitoring the amount of millimeters of
difference between the uper lid closed and open position (a regular technique for levator
muscles assessment).
a second levator muscle strength evaluation will include the study device. this device is
used for weight evaluation of objects. an object is measured by attaching it to the device
with a metal hook and a string. the device is hand held.
for measurements of the upper lid force the device will be temporarily attached to the upper
eyelid using a specially designed base made in the shape of the eyelid. the attachment will
be using a sterile medical tape (plaster). this sterile base is attached to the outer eyelid
and does not involve in any point any harm to the continuity of the skin, injections , harm
or contact to the eyeball or any other parts of the eye. this base is attached from its back
to a string witch attaches to the measuring device. the investigator holds the measuring
device and asks the patient to open and close his eyes. the force that is generated while
opening the upper lid is measured (in grams) by the device.
this evaluation will allow a unique first proper estimation of the true levator palpebra
strength. it will be compared to the levators' strength as estimated using the routine
techniques for assessing their efficacy.
the assessment will be made one time for each patient. after the measurement- the sterile
tape will be removed and will be disposed. no further interventions will be made for each
patient.
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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