KCT0006325
Completed
未知
A prospective, randomized, comparative clinical trial to evaluate the efficacy and safety of SRT(Selective Retina Therapy) with 'R:GEN' in patients with Central Serous Chorioretinopathy
ConditionsDiseases of the eye and adnexa
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Diseases of the eye and adnexa
- Sponsor
- The Catholic University of Korea, Yeouido St. Mary's Hospital
- Enrollment
- 44
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •In chronic CSC patients, as follows: (1\) the eye with persistent ( \= 3 months) subretinal fluid (SRF) involving the fovea in the optical coherence tomography (OCT) images of; (2\) focal or diffuse active hyperfluorescent leakages due to CSC on the fundus fluorescein angiography (FFA) image; (3\) between the age of 19 and 65 years.
Exclusion Criteria
- •(1\) the eye with best\-corrected visual acuity (BCVA) of 20/200 or worse (Snellen equivalent); (2\) other chorioretinal diseases such as choroidal neovascularization (CNV) and polypoidal choroidal vasculopathy (PCV); (3\) lens or vitreous opacity interrupting proper retinal imaging and laser treatment; (4\) RPE atrophy over 1,000 µm in diameter involving fovea; (5\) large PED over 300 µm in width or 100 µm in height; (6\) history of conventional laser photocoagulation or PDT for CSC; (7\) history of intravitreal injection of anti\-VEGF within 10 weeks prior to SRT; (8\) Use of systemic, periocular, intraocular corticosteroid within 1 year prior to SRT; (9\) use of spironolactone, acetazolamide, or ketoconazole within 2 months prior to SRT.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not yet recruiting
Phase 4
To assess the safety and performance of Cross-linked Hyaluronic Acid- Dermalfiller in people with all skin types, who need Lip Enhancement, Cheek boneAugmentation and Nasolabial fold improvementHealth Condition 1: L988- Other specified disorders of the skin and subcutaneous tissueCTRI/2019/09/021257Biotech Vision Care Pvt Ltd
Not yet recruiting
Phase 4
To compare and evaluate the safety, efficacy and refractive outcome of three different Hydrophilic Monofocal Intraocular Lens implanted to cataract patients.Health Condition 1: H259- Unspecified age-related cataractCTRI/2019/12/022318Biotech Vision Care Pvt Ltd
Not yet recruiting
Phase 4
A clinical study to compare the ayurvedic medicine Medhavati with allopathic medicine sertraline for the treatment of Depression.Health Condition 1: F321- Major depressive disorder, singleepisode, moderateCTRI/2020/06/025741ational Institute of Medical Sciences Research Jaipur
Not yet recruiting
Phase 1
To see the effect of Ayurveda drug in the eye disease.CTRI/2019/01/017035ational Institue of ayurveda
Recruiting
Not Applicable
A prospective randomized comparative clinical trial to evaluate the effectiveness of a digital intervention to reduce atopic symptoms and mental stress in patients with atopic dermatitisKCT0007127Yonsei University Health System, Gangnam Severance Hospital76