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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03433547
Other study ID # 2013meky013-3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 30, 2018
Est. completion date August 20, 2018

Study information

Verified date October 2018
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Full-thickness macular Hole associated with macular detachment is a one of the maculopathies of high myopia. There is controversy in the primary treatment for this situation. This study will compare the effects of macular buckling versus vitrectomy in a cohort of highly myopic eyes with this situation.


Description:

A randomized, open label, single center study comparing the efficacy of macular muckle + gas injection versus internal limiting membrane peeling + gas tamponade on full-thickness macular hole associated with macular detachment in eyes with high myopia.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date August 20, 2018
Est. primary completion date July 20, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- axial length = 26.5 mm or refractive error (spherical equivalent) = 8.0 diopter

- full-thickness macular hole

- macular retinal detachment

- evidence of posterior staphyloma on clinical examination

Exclusion Criteria:

- macular detachment which extended to the peripheral retina (i.e., extension beyond the major vascular arcades in more than one quadrant)

- a history of vitrectomy or scleral buckling

- intraocular active hemorrhage or inflammation

- any media opacity which precluded imaging or clinical evaluation of the macula

Study Design


Intervention

Procedure:
Buckle
Surgical procedures of macular buckling
Vitrectomy
Surgical procedures of small gauge vitrectomy
Other:
Limbal paracentesis
Drainage of aqueous fluid (0.1-0.2 ml) through limbal paracentesis
Gas injection
Inject gas ( C3F8 100%, 0.2ml-0.3ml) into vitreous cavity through pars plana.
Peeling internal limiting membrane
Peeling internal limiting membrane with forceps
Gas tamponade
Filling the vitreous cavity with gas (C3F8, 14%)

Locations

Country Name City State
China Zhongshan Ophthalmic Center, Sun Yat-sen University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Retinal re-attachment rate Successful rate of reattachment of macular retina after surgery 1 month
Secondary Macular hole status Closure rate of macular hole after surgery on optical coherence tomography 3 month
Secondary Post-operative best corrected visual acuity Best corrected visual acuity of the eyes after surgery 3 month
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