Cataract Surgery Clinical Trial
Official title:
Intraoperative Performance and Postoperative Outcomes Following Femtosecond Laser Assisted Cataract Surgery (FLACS) and Manual Phacoemulsification in Eyes With Shallow Anterior Chamber
Phacoemulsification in eyes with a shallow anterior chamber (ACD < 2.2mm) presents with
problems of safe access to the cataract and increased vulnerability of the endothelium and a
higher tendency of complications such as descemet's detachment and iris prolapse. A shallow
anterior chamber is also responsible for the high incidence of glaucoma and postoperative
complications after cataract surgery. Femtosecond assisted cataract surgery has made cataract
surgery safer and more predictable. The effective phacoemulsification time and
intra-operative manipulation is greatly reduced in FLACS. However phacoemulsification still
remains the most widely performed cataract surgery around the world. Post-operative outcomes
after phacoemulsification in patients having shallow anterior chamber have been extensively
reported in literature over the years.
There is no head to head comparison in terms of intraoperative performance and post-operative
outcomes between FLACS and phacoemulsification in eyes with shallow anterior chamber.
The aim is to compare the intra-operative performance and post-operative outcomes in eyes
undergoing femtosecond laser assisted cataract surgery versus eyes undergoing
phacoemulsification in eyes having shallow anterior chamber.
The study will bring an understanding on the question: Do patients undergoing Femtosecond
laser assisted cataract surgery behave differently from those undergoing phacoemulsification?
Inclusion Criteria:
- Age-related cataract
- Shallow Anterior Chamber (<2.5mm)
Exclusion Criteria:
-Ocular co-morbidity - corneal disorders, glaucoma, uveitis, previous ocular surgery
Surgical Technique :
- Standardized, Single Surgeon
- 2.2 mm clear corneal temporal incision
- FLACS Group : Capsulorhexis, Lens Fragmentation with femto laser
The investigators will be evaluating the following parameters:
1. Primary outcome measure Corneal thickness on day 1, week 1 and 1 month (Change in
corneal thickness of 15% from preop. will be considered significant).
2. Secondary outcome measures
- Corneal clarity -on day 1, week 1 and 1 month postoperatively
- Anterior chamber cells and flare (Hogan's criteria)
- Percentage change in endothelial cell density from preoperatively to 3 months
postoperatively
- Unaided visual acuity (distance) on day 1 and 1 month.
- Best corrected distance visual acuity 1 month postoperatively
3. Other Observations :
1) Cumulative Dissipated Energy (CDE) 2) Surgical time 3) Fluid used 4) Descemets membrane
detachment during surgery 5) Incidence of iris trauma 6) Any other intra-operative
complications
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02573610 -
Study of DE-108 Ophthalmic Solution in Patients Who Are Scheduled for Cataract Surgery
|
Phase 3 | |
Completed |
NCT02910362 -
Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Versus Alcon Phacoemulsification Machines
|
N/A | |
Recruiting |
NCT01193504 -
Randomized, Masked Comparison of Bromfenac and Besifloxacin BID With Either Prednisolone BID or Loteprednol 0.5% BID for Prevention of Retinal Thickening and CME Following Phacoemulsification
|
Phase 4 | |
Completed |
NCT01455233 -
2-Site Safety Study of Besivance Versus Vigamox Prophylactically in Routine Cataract Surgery
|
Phase 4 | |
Completed |
NCT01199510 -
Efficacy Evaluation of SYSTANE® ULTRA in Patients Scheduled for Cataract Surgery
|
Phase 4 | |
Completed |
NCT04146961 -
The PanOptix Trifocal IOL: A Study of Patient Satisfaction, Visual Disturbances, and Uncorrected Visual Performance
|
||
Completed |
NCT00585975 -
Efficacy and Safety of Bromfenac Ophthalmic Solution
|
Phase 2 | |
Completed |
NCT00406913 -
Prophylaxis Prior to Cataract Surgery Conjunctival Flora and Optimal Ocular Sterilization Technique Prior to Cataract Surgery
|
N/A | |
Not yet recruiting |
NCT04131335 -
Use of Prophylactic Lubricating Drops After Cataract Surgery
|
N/A | |
Recruiting |
NCT05331690 -
Cataract Surgery and Inflammation - the Role for Preoperative NSAIDs (Pre-CIN)
|
Phase 4 | |
Withdrawn |
NCT04563559 -
PREFERENTIAL Study
|
Phase 2/Phase 3 | |
Completed |
NCT04732351 -
Evaluation of the Active Sentry System During Cataract Surgery With the Centurion Phacoemulsifier
|
||
Completed |
NCT02128113 -
RTA 408 Ophthalmic Suspension for the Prevention of Corneal Endothelial Cell Loss Following Cataract Surgery - GUARD
|
Phase 2 | |
Completed |
NCT03873454 -
The Effects of Music on Perioperative Outcomes in Cataract Surgery
|
N/A | |
Completed |
NCT04769856 -
Impact of Non-fasting on Anxiety in Cataract Surgery
|
N/A | |
Withdrawn |
NCT00604305 -
Comperative Trial Between an Accommodative Iol and Monofocal Iol
|
N/A | |
Completed |
NCT05925894 -
Efficacy Mydrane ® for Cataract Surgery in Patients With Concomitant Primary Open Angle Glaucoma.
|
N/A | |
Not yet recruiting |
NCT06136780 -
Impact of Free Reading Glasses on Work and Visual Function Following Cataract Surgery in Honduras
|
N/A | |
Completed |
NCT04633954 -
Brimonidine for Subconjunctival Hemorrhage From Femtosecond Laser Assisted Cataract Surgery
|
N/A | |
Completed |
NCT03644875 -
Study of Etacoat in Patients With Cataract Surgery Via the Anterior Chamber
|