Clinical Study of Translocated Internal Limiting Membrane Flap Reposition for the Treatment of Idiopathic Macular Hole

NCT06063005 | Unknown

• 1 other identifier: XH-22-084
• Study Type: interventional
• Target: 76
• Locations: 1 country
• Sites: 1

Brief Summary

The main objective of this study is to evaluate the therapeutic effectiveness of the internal limiting membrane (ILM) peeling and translocation surgery compared to the conventional surgical approach for treating large idiopathic macular hole (IMH) through a well-designed prospective randomized controlled clinical trial. This study aims to compare the new surgical approach to the conventional approach in terms of improving visual function, promoting macular retinal anatomical healing, and enhancing patients' quality of life. By conducting this prospective clinical trial, establishing a database, and generating clinical reports and evidence-based medicine on the therapeutic efficacy of the ILM peeling and translocation surgery for large IMH.

Conditions

Macular Holes

Outcome Measures

Primary Outcomes (1)

• Best Corrected Visual Acuity

  The best corrected visual acuity indicates the best visual acuity with proper refractive correction.

  1 week, 1 month, 3 months, 1 years, 2 years after the operation

Secondary Outcomes (1)

• Closure rate

  1 week, 1 month, 3 months, 1 years, 2 years after the operation

Study Arms (2)

Translocation

EXPERIMENTAL

Procedure: Translocation ILM Flap

Peeling

ACTIVE COMPARATOR

Procedure: ILM Peeling

Interventions

Translocation ILM Flap PROCEDURE

After vitrectomy, the ILM was dissected from the macula to the vascular arch, and the retina in the fissure area was fully released to make an MH-centered, approximately 2DD-square, ILM flap with a tip (approximately 500μm wide) above; the ILM flap was transposed approximately 25-30 degrees along the tip to the inferior temporal area with the assistance of heavy water, and a total of 1ml of perfluorodecalin fluid (heavy water) was injected to cover the MH area with the ILM flap, and the original ILM defect area corresponding to the MH was transposed to the outside of the MH. The heavy water is replaced by liquid/gas exchange. Ophthalmic 13% perfluoropropane gas (AL.CHI.MI.A. Srl) was chosen as the postoperative intraocular filling.

Translocation

ILM Peeling PROCEDURE

After vitrectomy, internal limiting membrane peeling up to the vascular arcade, thorough loosening of the macular hole area of the retina, and fluid/gas exchange. An eye-specific 13% perfluoropropane gas (AL.CHI.MI.A. Srl) was chosen for intraocular tamponade after the operation.

Peeling

Eligibility Criteria

• Age: 55 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Participants who can understand the purpose of this clinical trial, volunteer to participate, sign an informed consent form, and can complete the postoperative follow-up on time.
• Participants diagnosed with idiopathic macular hole (IMH).
• Based on OCT scans, the minimum horizontal diameter of the macular hole is \>500 and \<900 µm.
• Participants with an axial length \<26.0mm and a myopic degree lower than 6D.
• For participants with bilateral macular holes, the eye with a larger hole diameter will be included.

You may not qualify if:

• Patients with the following retinal disorders: age-related macular degeneration, epi-macular membrane neovascularization, non-macular retinal tears, lesions of the retinal pigment epithelium and choroid, inherited or degenerative retinal diseases, optic neuropathies, retinal vascular diseases; patients with large macular holes accompanied by retinal detachment;
• Patients with high myopia (axial length ≥ 26.0mm and myopia exceeding 6D);
• Patients with a history of ocular trauma or retinal laser treatment;
• Patients with glaucoma, ocular infections, inflammations, tumors, corneal diseases, or amblyopia;
• Patients with contraindications to vitrectomy;
• Patients with severe or unstable systemic diseases;
• Patients with a fasting blood glucose level ≥ 9mmol/L before surgery;
• Patients who participated in other clinical trials involving drugs or medical devices within 30 days prior to screening;
• Patients with a history of intraocular surgery within 3 months prior to screening;
• Patients with reduced visual function or vision in the contralateral eye as determined by the investigator;
• Patients who are not considered suitable for enrollment by the investigator for other reasons.

Sponsors & Collaborators

• Xinhua Hospital, Shanghai Jiao Tong University School of Medicine: lead
• Shanghai Municipal Science and Technology Commission: collaborator

Study Sites (1)

Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, 200000, China

RECRUITING

MeSH Terms

Conditions

Retinal Perforations

Condition Hierarchy (Ancestors)

Retinal Diseases; Eye Diseases

Study Officials

• Peiquan Zhao, Dr.

  Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine Shanghai

  STUDY CHAIR

Central Study Contacts

Peiquan Zhao, Dr.

CONTACT

0086 13311620396; zhaopeiquan@xinhuamed.com.cn

Jiao Lyu, Dr.

CONTACT

0086 13564910954; cherryfcl@126.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: September 25, 2023
• First Posted: October 2, 2023
• Study Start: July 1, 2022
• Primary Completion: May 1, 2025
• Study Completion: June 30, 2025
• Last Updated: October 30, 2023

Record last verified: 2023-10

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)