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CTRI Number  CTRI/2024/04/065348 [Registered on: 08/04/2024] Trial Registered Prospectively
Last Modified On: 23/07/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Efficacy of Rho-Kinase inhibitor in Post-operative Striate Keratopathy 
Scientific Title of Study   Safety and efficacy of rho-kinase inhibitor for treatment of postoperative striate keratopathy. 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Keerti Wali 
Designation  Assistant professor 
Affiliation  SHRI B M PATIL MEDICAL COLLEGE, HOSPITAL AND RESEARCH CENTER, VIJAYAPURA, KARNATAKA 
Address  OPD 13, Department of Ophthalmology, BLDE Hospital Solapur Road, Vijayapura Karnataka

Bijapur
KARNATAKA
586101
India 
Phone  8722289221  
Fax    
Email  keertignec14@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Keerti Wali 
Designation  Assistant professor 
Affiliation  SHRI B M PATIL MEDICAL COLLEGE, HOSPITAL AND RESEARCH CENTER, VIJAYAPURA, KARNATAKA 
Address  Department of Ophthalmology, SHRI B M PATIL MEDICAL COLLEGE, SOLAPUR ROAD, VIJAYAPURA KARNATAKA

Bijapur
KARNATAKA
586101
India 
Phone  8722289221  
Fax    
Email  keertignec14@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Keerti Wali 
Designation  Assistant professor 
Affiliation  SHRI B M PATIL MEDICAL COLLEGE, HOSPITAL AND RESEARCH CENTER, VIJAYAPURA, KARNATAKA 
Address  Department of Ophthalmology, Shri B M Patil Medical College, Solapur Road

Bijapur
KARNATAKA
586101
India 
Phone  8722289221  
Fax    
Email  keertignec14@gmail.com  
 
Source of Monetary or Material Support  
Shri B M Patil Medical College, Solapur road, Vijayapura 
 
Primary Sponsor  
Name  BLDE UNIVERSITY 
Address  Shri B M Patil Medical College, Solapur Road, Vijayapura, Karnataka - 586103 
Type of Sponsor  Private medical college 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Keerti Wali  Shri B M Patil Medical College  Ophthalmology department , BLDE hospital, Solapur road
Bijapur
KARNATAKA 
8376934338

keertignec14@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
SHRI B. M. PATIL MEDICAL COLLEGE,HOSPITAL AND RESEARCH CENTRE, VIJAYAPURA  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: H590||Disorders of the eye following cataract surgery,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Ripasudil   Topical eyedrops BD for 5 days  
Intervention  Sodium chloride   Topical eyedrops QID for 5 days  
 
Inclusion Criteria  
Age From  50.00 Year(s)
Age To  80.00 Year(s)
Gender  Both 
Details  a) Striate keratopathy post uneventful cataract surgery [Both SICS & Phacoemulsification ]
b) Pre operative healthy clear cornea
c) No DMD
 
 
ExclusionCriteria 
Details  a) Pre existing corneal disorder
b) DMD
c) Aphakia, Vitreous in AC
d) Endophthalmitis
e) Known case of glaucoma
 
 
Method of Generating Random Sequence   Coin toss, Lottery, toss of dice, shuffling cards etc 
Method of Concealment   Case Record Numbers 
Blinding/Masking   Investigator Blinded 
Primary Outcome  
Outcome  TimePoints 
Improvement in corneal clarity with rho kinase inhibitor in striate keratopathy post cataract surgery  Cornea clarity will be checked at post operative day 1 ,day 5, day 10 and day 30  
 
Secondary Outcome  
Outcome  TimePoints 
Decrease in Striate keratopathy  7-15 DAYS POST OPEARTIVE DAYS 
 
Target Sample Size   Total Sample Size="300"
Sample Size from India="300" 
Final Enrollment numbers achieved (Total)= "300"
Final Enrollment numbers achieved (India)="300" 
Phase of Trial   Phase 3 
Date of First Enrollment (India)   15/04/2024 
Date of Study Completion (India) 31/05/2025 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) 31/05/2025 
Estimated Duration of Trial   Years="1"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details
Modification(s)  
N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary
Modification(s)  

Aim: To study the safety and efficacy of rho-kinase inhibitor in the treatment of post operative striate keratopathy

Objectives:

1.To help improve compliance with monotherapy

2.To aid in faster recovery of the patient

INTRODUCTION:

Striate keratopathy and raised intraocular pressure are common complications of cataract surgery. Endothelial cells maintain the relative state of dehydration in cornea and thus maintain the transparency. Any damage to endothelial cells intraoperatively may present as corneal edema. This damage may have a multifactorial causation like instrumentation, toxic solutions or ultrasonic energy used for phacoemulsification.

Hypertonic saline in combination with oral steroids and drugs to lower the intraocular pressure are the current main stay for treatment of striate keratopathy.

This treatment is only symptomatic and does not have any effect on endothelial cell function. Ripasudil is a Rho-kinase inhibitor which have been formulated as eye drops that have been approved for clinical use. Ripasudil since 2014 has been available in Japan for the treatment of glaucoma. Rho-kinase inhibitors have been found effective in the treatment of glaucoma and endothelial cells disorders. They help improve endothelial cell functionality and not just symptomatic treatment.

The effectiveness of rho-kinase inhibitors for corneal endothelium protection has been established in fields such as regenerative medicine, in which human corneal endothelial cell injection with a rho-kinase inhibitor was able to treat bullous keratopathy (BK) without conventional keratoplasty.  Limiting the treatment to one drug which would effectively have endothelial cell protection action and intraocular pressure lowering effect would increase patient compliance and give better outcomes.

Ripasudil(0.4%) is currently approved for use in Japan and Korea while Netarsudil is approved for use in USA and Canada . Ripasudil studies have been proven to shown effective along with less to no side effects.

Therefore the rho-kinase chosen for this study is ripasudil.

This study will   give an improved understanding of the safety and efficacy of rho-kinase inhibitors in comparison to current conventional treatment. It will help to quantify the occurrence of secondary glaucoma and the patients requiring DSEK post the use and disallowance of rho-kinase inhibitors in case and control subjects respectively

STUDY DESIGN- A CASE CONTROL STUDY

SOURCE OF DATA:

POST OPERATIVE CASES OF STRIATE KERATOPATHY IN IPD OF DEPARTMENT OF OPHTHALMOLOGY AT B.L.D.E. (DEEMED TO BE UNIVERSITY)’s S.H.R.I. B.M. PATIL MEDICAL COLLEGE, HOSPITAL AND RESEARCH CENTRE, VIJAYAPURA.

DURATION OF STUDY: 2 years

METHOD OF COLLECTION OF DATA:

 A case control study would be carried out on patients with post operative striate keratopathy attending the in-patient department of ophthalmology, B.L.D.E.’s Shri B.M. Patil Medical College, Hospital and Research Centre. As a standard protocol, all post operative cataract patients would be investigated for striate keratopathy. A clinical diagnosis of striate keratopathy is established by the presence of corneal edema with Descemet’s folds after cataract surgery in an eye with a relatively healthy and clear cornea and in the absence of obvious Descemet’s membrane detachment. They would be screened by complete ophthalmic examination, including

         Detailed history

         Best-corrected visual acuity

         Slit lamp examination

         Iop measurement

Grading for post MSICS corneal edema [13]

GRADE 0- clear cornea

GRADE 1 – hazy cornea

GARDE 2- foggy cornea/ DM folds/ striae, poor IOL reflex

GARDE 3 – cloudy cornea / DM folds/ striae, poor IOL reflex  , loss of iris details

GRADE 4 opacified cornea, DM folds/ striae, poor IOL reflex  , loss of pupillary  details

We would perform specular microscopy on day 1 and day 5  to compare the corneal endothelium before and post the use of ripasudil in post operative striate keratopathy with respect to following parameters

         Endothelial cell density

         Central corneal thickness

         Highest corneal thickness

 Inclusion Criteria-

a)      Striate keratopathy post uneventful cataract surgery [Both SICS & Phacoemulsification ]

b)      Pre operative healthy clear cornea

c)      No DMD

Exclusion Criteria-

a)      Pre existing corneal disorder

b)      DMD

c)      Aphakia, Vitreous in AC

d)      Endophthalmitis

e)      Known case of glaucoma

OUTCOMES EVALUATED

 PRIMARY OUTCOME

1. Decrease in CCT

2.Improvement of corneal clarity

3.Improvement of endothelial cell density

4.Duration of Visual improvement


SECONADARY OUTCOME

1.IOP control

2.Progression to PBK

3.To monitor adverse drug reactions

 

Patients with post operative striate keratopathy will be divided in two groups by simple random sampling

 GROUP 1

 Patients prescribed

·          Eye drops Ripasudil 0.4% BD

GROUP 2

  Patients prescribed

•          Sodium chloride 5% QID

•          Sodium chloride 6% HS

Brimonidine 0.15% and Timolol 0.5%


 
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