Epiretinal Membrane Clinical Trial
Official title:
27-gauge Vitrectomy Wound Integrity: a Prospective, Randomized Trial Comparing Angled Versus Straight Entry in Fluid-filled Vitrectomized Eyes
Verified date | November 2016 |
Source | Wills Eye |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To prospectively compare clinical outcomes using straight (perpendicular) versus angled
trocar insertion during 27 gauge pars plana vitrectomy surgery for epiretinal membrane
Primary Endpoints:
Sclerotomy suture rates and incidence of suture blebs at the end of 27 gauge MIVS.
Secondary Endpoints:
Rate of postoperative wound-related complications such as hypotony, choroidal detachments,
endophthalmitis, and sclerotomy-related retinal tears with a minimum follow-up of 30 days.
Status | Completed |
Enrollment | 30 |
Est. completion date | October 2016 |
Est. primary completion date | July 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients older than 18 years old undergoing 27 gauge vitrectomy surgery with membrane peel for epiretinal membrane - Willing and able to comply with clinic visits and study-related procedures - Provide signed informed consent Exclusion Criteria: - History of previous vitrectomy surgery in the study eye. - History of previous ocular surgery other than cataract extraction in the study eye. - Requirement of an air or gas (SF6, C3F8) bubble at the conclusion of 27 gauge MIVS surgery. - Aphakia, ACIOL, unstable PCIOL, and/or lenticular or zonular instability. - Glaucoma requiring IOP lowering medications. - Pre-existing ocular inflammation/uveitis. - Any concurrent intraocular condition in the study eye that, in the opinion of the investigator, could either require medical or surgical intervention during the 12 week study period to prevent or treat visual loss that might result from that condition. Examples include infectious conjunctivitis, keratitis, and/or scleritis. |
Country | Name | City | State |
---|---|---|---|
United States | Mid Atlantic Retina- Wills Eye Institute | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Wills Eye |
United States,
Chen E. 25-Gauge transconjunctival sutureless vitrectomy. Curr Opin Ophthalmol. 2007 May;18(3):188-93. Review. — View Citation
Gupta OP, Maguire JI, Eagle RC Jr, Garg SJ, Gonye GE. The competency of pars plana vitrectomy incisions: a comparative histologic and spectrophotometric analysis. Am J Ophthalmol. 2009 Feb;147(2):243-250.e1. doi: 10.1016/j.ajo.2008.08.025. Epub 2008 Oct 23. — View Citation
Oshima Y, Wakabayashi T, Sato T, Ohji M, Tano Y. A 27-gauge instrument system for transconjunctival sutureless microincision vitrectomy surgery. Ophthalmology. 2010 Jan;117(1):93-102.e2. doi: 10.1016/j.ophtha.2009.06.043. Epub 2009 Oct 31. — View Citation
Recchia FM, Scott IU, Brown GC, Brown MM, Ho AC, Ip MS. Small-gauge pars plana vitrectomy: a report by the American Academy of Ophthalmology. Ophthalmology. 2010 Sep;117(9):1851-7. doi: 10.1016/j.ophtha.2010.06.014. Review. — View Citation
Rizzo S, Barca F, Caporossi T, Mariotti C. Twenty-seven-gauge vitrectomy for various vitreoretinal diseases. Retina. 2015 Jun;35(6):1273-8. doi: 10.1097/IAE.0000000000000545. — View Citation
Spirn MJ. Comparison of 25, 23 and 20-gauge vitrectomy. Curr Opin Ophthalmol. 2009 May;20(3):195-9. doi: 10.1097/ICU.0b013e328329eaea. Review. — View Citation
Teixeira A, Rezende FA, Salaroli C, Souza N, Sousa BA, Allemann N. In vivo comparison of 23- and 25-gauge sutureless vitrectomy incision architecture using spectral domain optical coherence tomography. J Ophthalmol. 2013;2013:347801. doi: 10.1155/2013/347801. Epub 2013 Mar 4. — View Citation
Thompson JT. Advantages and limitations of small gauge vitrectomy. Surv Ophthalmol. 2011 Mar-Apr;56(2):162-72. doi: 10.1016/j.survophthal.2010.08.003. Epub 2011 Jan 14. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of sclerotomy site suturing and suture bleb formation | Minimum follow-up 30 days. | ||
Secondary | Rate of post-operative, wound related complications | Rate of complications including hypotony, choroidal detachment, and endophthalmitis | Minimum follow-up of 30 days | |
Secondary | Change in mean intraocular pressure | Measured in mm Hg by tonometry | Minimum follow-up of 30 days |
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