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Not yet recruitingNCT07883681Updated Oct 20, 2026

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

An interventional study of resection of superior rectus muscle in Dissociated Vertical Deviation, sponsored by Assiut University. Not yet recruiting. Open to participants aged 1 Day to 6 Months. Per ClinicalTrials.gov, last updated 2026-10-20.

Sponsored by Assiut University · Not applicable, Interventional, and Health services research

Updated Oct 20, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
1 Day to 6 Months
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Dissociated Vertical Deviation

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Keywords

  • DVD
03

In context

Strabismus

159 studies on the registry are indexed under Strabismus; 31 are open to participants now.

This study's planned enrollment of 30 is below the median of 60 across 98 interventional studies indexed under Strabismus.

Browse Strabismus studies →

Lead sponsor

Assiut University is the lead sponsor of 5,050 studies on the registry; 2,174 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 6 Months
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

    • Clinically manifest DVD of at least 15 prism diopters (PD) in the more affected eye, by prism and alternate cover test.

      • No previous surgery involving the vertical rectus or oblique muscles.
      • Parents or legal guardians willing to give written informed consent and to comply with scheduled follow-up.

Exclusion criteria

Exclusion Criteria:

    • Significant inferior oblique overaction or oblique dysfunction requiring simultaneous oblique muscle surgery.

      • Restrictive or paralytic strabismus, thyroid eye disease, or other orbital pathology affecting motility.
      • Craniofacial syndromes with abnormal extraocular muscle anatomy.
      • Systemic neuromuscular disease affecting extraocular muscle function.
      • Inability to obtain reliable preoperative or postoperative motility measurements due to poor cooperation.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Active comparator
    conventional SR recession

    graded recession of the superior rectus muscle alone, the amount graded to the preoperative DVD by the Tibrewal nomogram

    Other: resection of superior rectus muscle

  • Active comparator
    SR recession-resection

    a 2.5 mm segment of the SR resected, followed by recession of the muscle exceeding the resected length, graded to the preoperative DVD by the Tibrewal nomogram

    Other: resection of superior rectus muscle

  • Active comparator
    SR fenestration

    a central block of the SR muscle and its tendon removed close to the insertion, without disinsertion or scleral sutures, graded to the preoperative DVD

    Other: resection of superior rectus muscle

Interventions

  • Otherresection of superior rectus muscle

    resection of superior oplique muscle

06

What researchers measure

Primary outcomes

  1. Compare success rates in the 3 groups.

    Compare success rates in the 3 groups. Success is defined as absence of manifest DVD at final follow up

    Time frame: 6 months

Secondary outcomes

  1. recurrence at 6 months and reoperation rate.

    recurrence at 6 months and reoperation rate.

    Time frame: 6 months

  2. Torsional outcome

    fundus torsion (disc-fovea angle) before and after surgery.

    Time frame: 6 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 20, 2026
Show all 1 update
  1. Oct 20, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07883681
Lead sponsor
Assiut University
Responsible party
Abdelrahman Ahmed Shawki Roshdi (Assistant lecturer, Assiut University) — Principal investigator
First posted
Oct 20, 2026
Start date
Nov 1, 2026 (estimated)
Primary completion
Nov 1, 2028 (estimated)
Completion
Dec 1, 2028 (estimated)
Last update
Oct 20, 2026

Study contacts

Duaa Mohammed Ali Sayed zidan, Master degree
Contact
duaazidan75@gmail.com
01061541924

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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