Comparative Study Of Combined Recession-Resection And Fenestration of Superior Rectus Muscle for Treatment of Dissociated Vertical Deviation

StatusNot Yet Recruiting
PhaseNot applicable
Started

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Record History

  1. Study First Submitted
1,677 trials monitored
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Dissociated vertical deviation (DVD) is a slow, disconjugate upward drift of the non-fixating eye, usually with abduction and excyclotorsion, that does not obey Hering's law . It is uncommon in the general population but develops in about half to 90% of children with infantile esotropia . Its cause is uncertain, probably a supranuclear vertical vergence disturbance after early disruption of binocular fusion, which explains its association with infantile esotropia . Non-surgical treatment suits small or well-controlled deviations: refractive correction, amblyopia therapy . Surgery is indicated when the deviation is frequently manifest or cosmetically unacceptable . When inferior oblique overaction coexists, anterior transposition of the inferior oblique is the procedure of choice . In isolated DVD, surgery aims mainly to weaken the superior rectus (SR). Conventional graded SR recession is the most widely used , but large deviations may need 10 mm or more and undercorrection is common . Recession-resection resects part of the muscle then recesses it by a greater amount, raising the weakening effect , while fenestration removes a central block of muscle and tendon near the insertion without sutures and is simpler and faster . Other options are a posterior fixation (Faden) suture and Y-splitting . The evidence is weak: a Cochrane review found the published studies small and retrospective and asked for randomized trials , and the only comparison of three SR techniques allocated patients by deviation size rather than at random . No trial has compared fenestration with recession-resection in children with DVD.
Trial Details
NCT Number NCT07883681
Lead Sponsor Assiut University
Conditions
(from sponsor)
Dissociated Vertical Deviation
Related terms Strabismus
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov