Efficacy of Aurosling in Frontalis Sling Suspension Surgery
NCT ID: NCT00753831
Last Updated: 2012-07-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
16 participants
INTERVENTIONAL
2009-01-31
2009-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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1
Aurosling
Aurosling
Silicon rod to be used in frontalis suspension surgery
Interventions
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Aurosling
Silicon rod to be used in frontalis suspension surgery
Eligibility Criteria
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Inclusion Criteria
* Severe Ptosis (MRD\<0)
* Poor levator function (\<4mm by Berke's method)
* Myogenic Ptosis (Myasthenia gravis)
* Chronic progressive external ophthalmoplegia
* Neurogenic Ptosis (Third cranial palsy)
* Blepharospasm
* Ptosis caused by trauma
Exclusion Criteria
* Horners syndrome
* Blepharochalasis/Dermatochalasis
* Mechanical Ptosis
* Mild or Moderate Ptosis (MRD 1\>1)
* Good or fair levator function (\>4 mm by Berke's method)
* Previous Ptosis surgery
* Ptosis associated syndromes/Other anomalies including
* Marcus Gunn jaw winking syndrome
* Blepharophimosis syndrome
* Dry eye syndromes
* Corneal anesthesia
* Medical/Pediatric/Anesthesia condition contraindicating to surgery or anesthesia
* Nystagmus where adequate measurements could not be done
* Uncorrected vertical squint of any sort
ALL
No
Sponsors
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Aurolab
OTHER
Responsible Party
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Principal Investigators
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Usha Kim, DO, Dip NB
Role: PRINCIPAL_INVESTIGATOR
Aravind Eye Hospital, Madurai
Locations
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Aravind Eye Hospital
Madurai, Tamil Nadu, India
Countries
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Other Identifiers
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2PR1220827
Identifier Type: -
Identifier Source: org_study_id
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