Age-related Cataract Clinical Trial
Official title:
Comparison of Changes in Effective Lens Position of Different Types of Intraocular Lens
NCT number | NCT04443101 |
Other study ID # | SSOCT-ELP |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 1, 2019 |
Est. completion date | March 30, 2023 |
Cataract patients were implanted with different types of intraocular lenses for grouping. SSOCT scanning was used to measure ELP and optometry.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | March 30, 2023 |
Est. primary completion date | May 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 90 Years |
Eligibility | Inclusion Criteria: - a.Diagnosed as cataract; - b.Implanted intraocular lens: SN6CWS, Aspira-aA, MI60; - c.Cataract phacoemulsification and intraocular lens implantation. Exclusion Criteria: - a.Combined with corneal opacity, glaucoma, uveitis, retinal detachment and other eye diseases; - b.A history of intraocular surgery or trauma other than cataract surgery; - c.Intraoperative complications such as tearing of the capsule and IOL failure to implant; - d.Endophthalmitis, corneal endothelial decompensation and other postoperative complications; - e.Those with incomplete data collected during the follow-up period of postoperative patients. |
Country | Name | City | State |
---|---|---|---|
China | Ophthalmology and Optometry Hospital | Wenzhou | Zhejiang |
China | Wenzhou Medical University | Wenzhou | Zhejiang |
Lead Sponsor | Collaborator |
---|---|
Wenzhou Medical University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | effective lens position | Changes of effective lens position at different time points after cataract surgery | up to 3 months after cataract surgery |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04702802 -
Clinical Study to Evaluate the Safety of the Viscoelastic Substance PRO-149 When Used During Phacoemulsification, Compared to Healon® EndoCoat.
|
Phase 1 | |
Recruiting |
NCT05802550 -
Metabo-lipidomics of the Ocular Surface for Cataract Surgery
|
N/A | |
Recruiting |
NCT04246346 -
Effectiveness of Using Interactive Consulting System to Enhance Informed Choice
|
N/A | |
Recruiting |
NCT03340389 -
Dysfunctional Lens Index Serves as a Novel Surgery Decision Maker for Age-related Cataracts
|
N/A | |
Recruiting |
NCT04050644 -
Comparison of Treatment With Preservative-free Dexamethasone 0.1% (Monofree Dexamethason) and Diclofenac 0.1% (Dicloabak) Eye Drops Versus Preserved Dexamethasone 0.1% (Maxidex) and Diclofenac 0.1% (Voltaren Ophtha) Eye Drops After Cataract Surgery
|
Phase 4 | |
Not yet recruiting |
NCT05028530 -
Correlation Analysis of Lens Nucleus Density and Surgical Parameters Based on Ss-oct and Scheimpflug Technology
|
||
Completed |
NCT05573529 -
EDOF and Multifocal IOL Study
|
N/A | |
Recruiting |
NCT04711395 -
The Application of Lens Dysfunction Index (DLI) in the Timing of Age-related Cataract Surgery
|
||
Completed |
NCT04262596 -
Effectiveness of an Interactive Consulting System to Enhance Patients' Decision-making: A Randomized Controlled Trial
|
N/A | |
Recruiting |
NCT02817191 -
Effects of Holy-Comod and Tears Naturale Forte in Patients After Phaco+IOL
|
N/A | |
Completed |
NCT06266962 -
Comparing the Efficiency of Two Approaches in Patients at Risk of Developing Intraoperative Floppy Iris Syndrome
|
Phase 4 | |
Completed |
NCT05148741 -
Evaluation of Capsular Bag Shape Changes After Plate-haptic Intraocular Lens Implantation by SS-OCT
|
||
Active, not recruiting |
NCT03992807 -
A Decision Aid for Patients With Age-related Cataract
|
N/A | |
Recruiting |
NCT05255796 -
IOL-capsular Complex After Different Intraocular Lenses Implantation in Patients With High Myopia
|
N/A | |
Completed |
NCT04187157 -
Association Between Light Spectrum and Survival After Cataract Surgery
|
||
Withdrawn |
NCT04163926 -
Optometric Follow-up After Cataract Surgery
|
N/A |