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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04465188
Other study ID # P160948J
Secondary ID 2018-A01081-54
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date June 2023
Est. completion date January 2030

Study information

Verified date February 2023
Source Assistance Publique - Hôpitaux de Paris
Contact Pierre-Raphael ROTHSCHILD, MD, Phd
Phone +33 1 58 41 24 16
Email pierreraphael.rothschild@aphp.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether a scleral buckling surgical procedure performed on fellow eyes of patients with genetically confirmed Stickler syndrome can prevent the occurrence retinal detachment and/or severe vision loss of the study eye.


Description:

Stickler syndrome (STL) is a genetic disease affecting several organs. However the major risk is represented by the development of retinal detachment (RD). Up to 80% of patients present a RD and 25% to 80% have sequential bilateral RD. The surgical outcome of RD in this population is worse than that of the general RD population mainly because of the severity at diagnosis and the high frequency and severity of postoperative complications. Prevention has therefore emerged as a therapeutic option for this identifiable high-risk group of patients. Prevention has been proposed especially for the fellow (contralateral) eye of patients having presented a RD in their first eye and often lost vision as a consequence of retinal detachment in the first eye. The investigators hypothesize that a scleral buckling surgical procedure performed for the fellow eye of STL patients having recently presented a RD of the first eye could prevent the occurrence of bilateral RD and/or vision loss. Stickler patients are regularly diagnosed and followed-up in referral centers mainly in the context of a recent retinal detachment. They are proposed genetic testing as part of the standard of care. Genetically confirmed Stickler patients having recently presented (<24 months) a retinal detachment and treated as part of the standard care are eligible for this study. During the usual follow-up visits performed for their recent first RD operation they will be informed and offered to participate in the "STL-DR-PREV study" for the prevention of RD of their fellow eye. Patients in the intervention arm will undergo an encircling scleral buckle surgical procedure, which is a routine surgical procedure used for decades and still in use to treat RD that will be performed in the present study to prevent rather than to treat retinal detachment from a healthy eye of a patient having a genetically confirmed Stickler Syndrome.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date January 2030
Est. primary completion date January 2030
Accepts healthy volunteers No
Gender All
Age group 5 Years to 35 Years
Eligibility Inclusion Criteria: - Genetically confirmed Stickler Syndrome - Aged 5 to 35 - Recent retinal detachment in the non-study eye (<24 months) - Signed informed consent to participate in the study - Sufficient patient cooperation to perform a complete ophthalmologic examination including a dilated fundus examination Exclusion Criteria: - Any type of previous prevention (laser, cryotherapy, scleral buckle) for the study eye - Subclinical retinal rhegmatogenous detachment in the study eye. - Any other ocular disease unrelated to Stickler syndrome significantly affecting visual acuity (ETDRS BCVA<20/400). - Contraindications to general anesthesia - Posterior vitreoretinal traction on optical coherence tomography - Intraoperative detection of one or more of the above-mentioned non-inclusion criteria

Study Design


Intervention

Procedure:
Encircling scleral buckle surgical procedure
Encircling scleral buckle surgical procedure under general anesthesia

Locations

Country Name City State
France Hôpital Cochin Paris

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

References & Publications (5)

Abeysiri P, Bunce C, da Cruz L. Outcomes of surgery for retinal detachment in patients with Stickler syndrome: a comparison of two sequential 20-year cohorts. Graefes Arch Clin Exp Ophthalmol. 2007 Nov;245(11):1633-8. doi: 10.1007/s00417-007-0609-2. Epub 2007 Jun 20. — View Citation

Ang A, Poulson AV, Goodburn SF, Richards AJ, Scott JD, Snead MP. Retinal detachment and prophylaxis in type 1 Stickler syndrome. Ophthalmology. 2008 Jan;115(1):164-8. doi: 10.1016/j.ophtha.2007.03.059. Epub 2007 Aug 2. — View Citation

Carroll C, Papaioannou D, Rees A, Kaltenthaler E. The clinical effectiveness and safety of prophylactic retinal interventions to reduce the risk of retinal detachment and subsequent vision loss in adults and children with Stickler syndrome: a systematic review. Health Technol Assess. 2011 Apr;15(16):iii-xiv, 1-62. doi: 10.3310/hta15160. — View Citation

Fincham GS, Pasea L, Carroll C, McNinch AM, Poulson AV, Richards AJ, Scott JD, Snead MP. Prevention of retinal detachment in Stickler syndrome: the Cambridge prophylactic cryotherapy protocol. Ophthalmology. 2014 Aug;121(8):1588-97. doi: 10.1016/j.ophtha.2014.02.022. Epub 2014 May 1. — View Citation

Monin C, Van Effenterre G, Andre-Sereys P, Haut J. [Prevention of retinal detachment in Wagner-Stickler disease. Comparative study of different methods. Apropos of 22 cases]. J Fr Ophtalmol. 1994;17(3):167-74. French. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Best corrected visual acuity and retinal detachment rate Early Treatment Diabetic Retinopathy Study (ETRDS) best corrected visual acuity (BCVA) and dilated funduscopic examinations at scheduled follow-up (every 6 months) 5 years
Secondary Rate of retinal breaks 5 years
Secondary Rate of intravitreal hemorrhage 5 years
Secondary Outcome in prevention-failed study eyes outcome of surgery for RD in the study eye of patients for whom prevention failed and had to be operated on for RD repair of the study eye 5 years
Secondary Effect of add-on cryotherapy To assess within the experimental arm whether patients having had cryotherapy as part (allowed by the protocol at the surgeon's discretion in addition to the standard procedure) of the scleral buckling procedure present a decrease in the rate of RD as compared to buckled patients without cryotherapy 5 years
See also
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