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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02201706
Other study ID # MER201407
Secondary ID MER201407
Status Recruiting
Phase N/A
First received July 15, 2014
Last updated May 5, 2015
Start date October 2013
Est. completion date July 2017

Study information

Verified date May 2015
Source Sun Yat-sen University
Contact Xiaofeng Lin, Dr
Phone 02087330000
Email linxiaof@mail.sysu.edu.cn
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Retinal re-detachment in silicone oil filled eye, especially in the traumatic eye, is a complex retinal detachment with poor prognosis.

In this study, the investigators try to apply a modified surgery as Multi-electrocoagulation retinectomy to reattach the retina. Here the investigators aimed to explore the safety and efficacy of this new surgical approach


Description:

The relaxing retinectomy is a useful surgery for retinal re-detachment in eyes with silicone oil filled. However, it has some obvious disadvantages such as the cut of the normal retina surrounding, leaving a large area of retinal deficiency and significant exposure of retinal pigment epithelium and choroid membranes.

In this study, we try to apply a modified surgery named Multi-electrocoagulation retinectomy to re-attach the retina.

Instead of cutting through the proliferated retina directly, this new surgical approach adopts to cut the retina apart in a honeycomb shape with the help of electrocoagulation.

In this way, we not only relax the traction of the proliferative membranes, but also reserve the rest retina to cover the RPE layers.

Based on the hypothesis above, we are aiming to explore the safety and efficacy of this new surgical approach


Recruitment information / eligibility

Status Recruiting
Enrollment 9
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender Both
Age group 5 Years to 60 Years
Eligibility Inclusion Criteria:

1. Age 5-60 years, male or female

2. The primary retinal detachment was caused by ocular trauma, and the vitreous body is filled with silicone oil now.

3. The presence of inferior retinal re-detachment located among 3-9 o'clock.

Exclusion Criteria:

1. The primary retinal detachment was not caused by ocular trauma.

2. Location of the re-detached retina is not mainly in the inferior of the eye.

3. The fundus is unobservable because of severe corneal opacity.

4. The contralateral eye is non-functional

5. Serious heart, lung, liver and kidney dysfunction

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Multi-electrocoagulation retinectomy
a modified surgery named "multi-electrocoagulation retinectomy" to re-attach the retina. All the single surgical technique and devices involved in this modified surgery are used commonly in clinic. Base on this, the investigator changes the traditional sequence of these single surgical techniques, and combine them into a new surgical process.

Locations

Country Name City State
China Zhongshan Ophthalmic Center of Sun yat-sen Universtiy Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

References & Publications (3)

de Silva DJ, Kwan A, Bunce C, Bainbridge J. Predicting visual outcome following retinectomy for retinal detachment. Br J Ophthalmol. 2008 Jul;92(7):954-8. doi: 10.1136/bjo.2007.131540. Epub 2008 Jun 12. Review. Erratum in: Br J Ophthalmol. 2008 Aug;92(8):1159. — View Citation

Han DP, Lewis MT, Kuhn EM, Abrams GW, Mieler WF, Williams GA, Aaberg TM. Relaxing retinotomies and retinectomies. Surgical results and predictors of visual outcome. Arch Ophthalmol. 1990 May;108(5):694-7. — View Citation

Romaniuk VM. Ocular trauma and other catastrophes. Emerg Med Clin North Am. 2013 May;31(2):399-411. doi: 10.1016/j.emc.2013.02.003. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary retina reattachment rate 3 months after the surgery No
Secondary visual acuity Before surgery, 3days,1 week, 2 weeks, 4 weeks, 3 months and 6 months after surgery. Yes
Secondary Intraocular pressure Before surgery, 3days,1 week, 2 weeks, 4 weeks, 3 months and 6 months after surgery. Yes
Secondary The degree of recurrent PVR Before surgery, 3days,1 week, 2 weeks, 4 weeks, 3 months and 6 months after surgery. Yes
Secondary The incidence of intraocular hemorrhage Before surgery, 3days,1 week, 2 weeks, 4 weeks, 3 months and 6 months after surgery. Yes
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