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IOBT Versus IO-Rec for Hypertropia With IOOA (IIHIOOA)

Inferior Oblique Muscle Belly Transposition (IOBT) Versus Inferior Oblique Muscle Recession (IO-rec) on Versions and Vertical Alignment for Primary Position Hypertropia With Inferior Oblique Overaction

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05415553
Enrollment
190
Registered
2022-06-13
Start date
2022-07-01
Completion date
2025-06-30
Last updated
2022-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertropia, Inferior Oblique Overaction

Keywords

Inferior oblique muscle belly transposition, Inferior oblique muscle recession, Inferior oblique overaction

Brief summary

This is a multi-center, randomized double-blind controlled trial to compare the effectiveness of IOBT with IO-Rec for the treatment of hypertropia with IOOA. Specific Aim 1 (Primary): To study the suboptimal surgical rates between IOBT and IO-Rec for the treatment of hypertropia with IOOA. Specific Aim 2 (Secondary): To compare the surgical successful rate of IOBT with IO-Rec for the treatment of hypertropia with IOOA.

Detailed description

Using conventional surgical procedures, such as myectomy or recession of inferior oblique muscle, higher postoperative vertical overcorrection due to contralateral concealed IOOA were observed in mild primary position hypertropia with unilateral IOOA. To achieve better outcome, IOBT was introduced. Yang et al. firstly reported that IOBT might be a useful alternative surgical treatment for patients with primary position hypertropia of less than 5△ that was associated with IOOA. Recently, our study has reported that IOBT achieved satisfactory outcomes in patients with mild primary position vertical deviation (≤10△) with unilateral IOOA, without any risk of overcorrection of vertical deviation and contralateral IOOA. Although our results are promising, there is no enough evidence to recommend IOBT for primary position hypertropia with inferior oblique overaction. A large randomized trial is needed to compare the surgical successful rate and suboptimal surgical outcomes of IOBT with IO-Rec for primary position hypertropia with inferior oblique overaction. The proposed trial will be conducted in 9 different study sites working in the field of pediatric ophthalmology and strabismus. Each site will have one certified surgeon to do all surgeries. For IOBT, the whole belly of inferior oblique muscle is secured with a 6-0 absorbable suture, and then anchors to the sclera 5 mm behind the temporal insertion of the inferior rectus muscle. For IO-Rec, the insertion of inferior oblique muscle is excised and secured with a 6-0 absorbable suture, and then anchors to the sclera 4 mm behind and 2 mm beside the temporal insertion of the inferior rectus muscle.

Interventions

PROCEDUREIOBT

Surgery of inferior oblique muscle belly transposition for treatment of primary position hypertropia with inferior oblique overaction

PROCEDUREIO-Rec

Surgery of inferior oblique muscle recession for treatment of primary position hypertropia with inferior oblique overaction

Sponsors

Children's Hospital of Fudan University
CollaboratorOTHER
Shandong Provincial Hospital
CollaboratorOTHER_GOV
Shanxi Eye Hospital
CollaboratorOTHER
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Tianjin Eye Hospital
CollaboratorOTHER
Renmin Hospital of Wuhan University
CollaboratorOTHER
Xiamen Eye Center of Xiamen University
CollaboratorUNKNOWN
Kunming Aier Eye Hospital
CollaboratorUNKNOWN
Eye & ENT Hospital of Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
4 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 4 years at the time of surgery; * Vertical deviation (VD) in primary position (5△ ≤ VD ≤ 10△) * IOOA for three following situations: 1. IOOA +1 for the operative eye and IOOA - for the follow eye; 2. IOOA +2 for the operative eye and IOOA ± for the follow eye; 3. IOOA +2 for the operative eye and IOOA +1 for the follow eye; * Without amblyopia

Exclusion criteria

* Histories of strabismus surgery or botulinum toxin injection; * Histories of intraocular surgery or refractive surgery; * Restrictive or paralytic strabismus; * Ocular disease other than strabismus or refractive error; * Craniofacial malformations affecting the orbits; * Significant neurological disorders

Design outcomes

Primary

MeasureTime frameDescription
Suboptimal surgical rateat 12 monthsSuboptimal surgical cases/total cases. Suboptimal surgical outcomes include vertical undercorrection, vertical overcorrection and antielevation syndrome.

Secondary

MeasureTime frameDescription
Surgical successful rateat 12 monthSurgical successful cases/total cases. The successful criterion is without any vertical deviation in primary position at distance and without IOOA postoperatively.

Countries

China

Contacts

Primary ContactChen Zhao
dr_zhaochen@163.com+86-021-6437-7134
Backup ContactWenqing Zhu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026