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CTRI Number  CTRI/2020/05/025095 [Registered on: 11/05/2020] Trial Registered Prospectively
Last Modified On: 06/05/2020
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Surgical/Anesthesia 
Study Design  Other 
Public Title of Study   COMPARISON OF GLAUCOMA SURGERY(TRABECULECTOMY) IN OPEN ANGLE GLAUCOMA AND CLOSED ANGLE GLAUCOMA 
Scientific Title of Study   COMPARATIVE EVALUATION OF TRABECULECTOMY IN PRIMARY OPEN ANGLE GLAUCOMA AND PRIMARY ANGLE CLOSURE GLAUCOMA 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Umesh 
Designation  Postgraduate student 
Affiliation  Maulana Azad Medical College 
Address  Room no 310 third floor Lok Nayak Resident Doctors Hostel Maulana Azad Medical College New Delhi 110002

Central
DELHI
110002
India 
Phone  8802393391  
Fax    
Email  22494drumesh@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Kirti Singh 
Designation  Director Professor 
Affiliation  Maulana Azad Medical College 
Address  Room no 205 second floor Ward and Emergency Building Guru Nanak Eye Center New Delhi 110002

Central
DELHI
110002
India 
Phone  9968604334  
Fax    
Email  mail4kirti@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Kirti Singh 
Designation  Director Professor 
Affiliation  Maulana Azad Medical College 
Address  Room no 205 second floor Ward and Emergency Building Guru Nanak Eye Center New Delhi 110002

Central
DELHI
110002
India 
Phone  9968604334  
Fax    
Email  mail4kirti@gmail.com  
 
Source of Monetary or Material Support  
Maulana Azad Medical College 
 
Primary Sponsor  
Name  Maulana Azad Medical College 
Address  Maulana Azad Medical College Bahadur Shah Zafar Marg New Delhi 110002 
Type of Sponsor  Government 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 Umesh  Guru Nanak Eye Centre  Room No 116 Glaucoma Clinic OPD Building Guru Nanak Eye Centre New Delhi 110002
Central
DELHI 
8802393391

22494drumesh@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: H401||Open-angle glaucoma, (2) ICD-10 Condition: H402||Primary angle-closure glaucoma,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Not Applicable  Not Applicable 
Intervention  Trabeculectomy and Conjunctival biopsy  Suitable patients meeting the inclusion criteria will be enrolled in the study and evaluated on the above said parameters prior to the surgery. Patients will be divided into two groups. Group 1- POAG undergoing trabeculectomy. Group 2- PACG undergoing trabeculectomy. Trabeculectomy with releasable sutures with use of mitomycin C 0.02% for 2 min restricted to patients younger than 50 years, would be performed by the same surgeon.A conjunctival frill incision followed by a triangular superficial flap of 4 X 4mm followed by 2X1 mm sclerostomy by Kelly Descemet punch and large peripheral iridectomy would be done. The scleral flap would be closed by one fixed and 2 releasable sutures. Conjunctival closure by 8-0 nylon would be followed by on table titration of bleb. The conjunctival tissue biopsy would be taken from inferior conjunctiva of size 2X3 mm at the time of trabeculectomy. The tissue would be immediately fixed in 10% buffered formalin and processed as per protocol to have formalin fixed paraffin embedded (FFPE) tissue. Thin sections of 5 microns will be cut. Care would be taken to orient sections to obtain epithelium and stroma. Cut sections would be stained for hematoxylin and eosin, PAS with Diastase with Alcian blue. Immunohistochemistry would be performed as per protocol of various primary antibodies. PRIMARY ANTIBODIES a) T Cells -CD3, CD5 b) Macrophages-CD68 c) Mast cell-CD117 d) Fibroblast-Vimentin Bleb functionality and morphology would be assessed by a)Intraocular pressure control b) Slit lamp examination- IBAGS classification c) Anterior segment Ocular coherence tomography (AS SOCT) Patients would then be subsequently evaluated on post- operatively on Day 1, Day 7, 1 month, and 4 months.  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  75.00 Year(s)
Gender  Both 
Details  1) Uncontrolled primary glaucoma requiring trabeculectomy
2) Age>18 years
3) Patient willing to follow up for minimum 4 monthes  
 
ExclusionCriteria 
Details  1)Prior incisional surgery involving conjunctiva
2)Dry eyes
3)Use of long term steroids
4)Chronic ocular pathology like keratitis, uveitis, episcleritis and scleritis 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
1)Bleb functionality and morphology
2)Conjunctival cell profile  
To be assessed at 1 week, 1 month and 4 monthes post operatively  
 
Secondary Outcome  
Outcome  TimePoints 
Conjunctival inflammation correlation with bleb function and morphology  To be assessed at 1 week, 1 month and 4 monthes post operatively  
 
Target Sample Size   Total Sample Size="60"
Sample Size from India="60" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 2/ Phase 3 
Date of First Enrollment (India)   11/05/2020 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   Not yet published 
Individual Participant Data (IPD) Sharing Statement

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

Brief Summary  

Glaucoma is the leading cause of irreversible blindness in the world with an estimated 34 millionpeople worldwide being affected by 2040.Glaucoma can be classified into primary and secondary which decide treatment protocol. Primary angle closure glaucoma (PACG) is a major form of glaucoma in east Asia while primary open angle glaucoma (POAG)  predominates in  Caucasians and Africans. Recent glaucoma prevalence studies in south India found that prevalence of PACG is high at 4.32%. It is estimated that PACG blinds more people than POAG in absolute terms although the number of POAG worldwide is higher. By 2020 PACG would affect 20 million people and an estimate of 5.3 million could be blind.

Trabeculectomy creates a new path for aqueous outflow which bypasses the diseased trabecular meshwork and forms a bleb. Bleb functionality and longevity is determined by extent of subconjunctival fibrosis, the latter being the commonest cause of bleb failure. Conjunctiva being the reservoir of fibroblast recruitment at the time of filtration surgery, its preoperative health is likely to play a crucial role in tissue behavior in response to trauma of surgery.

Primary angle closure glaucoma PACG eyes have been documented to present with higher Intraocular pressure (IOP). Recurrent bouts of high IOP in these eyes result in ischemia, reperfusion injury, manifesting with iris atrophy and subclinical inflammation in conjunctiva of ACG eyes. Anatomical aspects of ACG with smaller eyeballs, smaller palpebral fissure and shallow fornices, thicker iris and thicker lens make trabeculectomy challenging. Concomitant tear film dysfunction subsequent to long term use of anti-glaucoma medications (AGM) resulting in deranged conjunctival milieu reduces chance of bleb survival. Due to the above reasons, filtering surgery in PACG behaves differently from POAG eyes.

Keeping the immensity of PACG in India, it’s tendency to cause more blindness, its surgical differences in mind, we propose to study trabeculectomy outcomes in angle closure glaucoma v/s open angle glaucoma with respect to bleb morphology and function. Conjunctival cellular profile would be studied for cell markers of inflammation and linkage if any, to bleb survival.

LACUNAE IN EXISTING KNOWLEDGE

1.     To the best of our knowledge there is paucity of data in Indian population comparing trabeculectomy outcomes in Primary Angle Closure Glaucoma and Primary Open Angle Glaucoma.

2.     Paucity of data on relationship of conjunctiva cellular profile with respect to bleb  functionality and morphology in Primary Angle Closure Glaucoma eyes.

AIMS AND OBJECTIVES

1)     To compare surgical outcome of trabeculectomy in Primary Angle Closure Glaucoma  and Primary Open Angle Glaucoma eyes.

2)     Correlate conjunctival cellular profile with bleb function and morphology.

 

 


 

MATERIAL AND METHODS

STUDY TYPE: Prospective comparative study

SETTING: Department of Ophthalmology, Guru Nanak Eye Centre, Maulana Azad Medical College & associated hospitals, New Delhi

STUDY DESIGN: Hospital based, prospective comparative study

SAMPLE SIZE: The study of Maheshwari, D et al in 2019 observed that mean intraocular pressure at 6 months in open angle glaucoma was 10.5 ± 2.6 and in angle closure glaucoma was 12 ± 3.8. Taking these values as reference, the minimum required sample size with 80%power of study and 5% level of significance is 74 patients in each study group. So total sample size taken is 150 (75 patients per group).

SAMPLE SIZE CALCULATION

Formula used is:

For comparing mean of two groups

                     N>=2(standard deviation)2 *(Zα + Zβ)2 (mean difference)2​

Where Zα is value of Z at two sided alpha error of 5% and Zβ is value of Z at power

of 80% and mean difference is difference in mean values of two groups.

Pooled standard deviation= Sqrt(((S1)2+(S2)2)/2)

          Where S1 is standard deviation of 1 group.

          And S2 is standard deviation of other group.

 Calculations:

Pooled standard deviation=sqrt(((2.6)2+(3.8)2)/2)  =3.25

N>=2(3.25)2 *(1.96 + .84)2

                           (1.5)2​>=73.61=74(approx.)

But due to time constraints we will take a convenience sample size of 60 ,that is 30 POAG patients and 30 PACG patients.

INCLUSION CRITERIA

1.     Uncontrolled  primary glaucoma requiring trabeculectomy

2.     Age >18 years

3.     Patient willing to follow up for minimum 4 months.

   EXCLUSION CRITERIA

1.     Prior incisional surgery involving conjunctiva

2.     Dry eyes

3.     Use of long term topical steroids

4.     Chronic ocular pathology like keratitis, uveitis, episleritis and scleritis.

 

 

OUTCOMES EVALUATED

PRIMARY OUTCOME

1) Bleb functionality and morphology

2) Conjunctival cell profile

 

SECONDARY OUTCOME

1) Conjunctival inflammation correlation with bleb function and morphology

 

STUDY PROTOCOL

Suitable patients meeting the inclusion criteria will be enrolled in the study and evaluated on the above said parameters prior to the surgery. Patients will be divided into two groups.

Group 1- POAG undergoing trabeculectomy.

Group 2- PACG undergoing trabeculectomy.

Trabeculectomy with releasable sutures with use of mitomycin C 0.02% for 2 min restricted to patients younger than 50 years, would be performed by the same surgeon.Aconjunctival frill incision followed by a triangular superficial flap of 4 X 4mm followed by 2X1 mm sclerostomy by Kelly Descemet punch and large peripheral iridectomy would be done. The scleral flap would be closed by one fixed and 2 releasable sutures. Conjunctival closure by   8-0 nylon would be followed by on table titration of bleb.

The conjunctival tissue biopsy would be taken from inferior conjunctiva of size 2X3 mm at the time of trabeculectomy. The tissue would be immediately fixed in 10% buffered formalin and processed as per protocol  to have formalin fixed paraffin embedded (FFPE) tissue. Thin sections of 5 microns will be cut. Care would be taken to orient sections to obtain epithelium and stroma. Cut sections would be stained for hematoxylin and eosin, PAS with Diastase with Alcian blue. Immunohistochemistry would be performed as per protocol of various primary antibodies.

PRIMARY ANTIBODIES

a)     T Cells -CD3, CD5

b)     Macrophages-CD68

c)     Mast cell-CD117

d)     Fibroblast-Vimentin

Bleb functionality and morphology would be assessed by

a)Intraocular pressure control

b)  Slit lamp examination- IBAGS classification

c) Anterior segment Ocular coherence tomography (AS SOCT)

Patients would then be subsequently evaluated on post- operatively on Day 1, Day 7, 1 month, and 4 months.

 

 

 

 

 

 

 

 

Parameters evaluated:

●      Intraocular pressure(IOP): measured by Goldman applanation tonometry (GAT) 

●      Conjunctival  biopsy : Cellular profile : macrophages(CD68), lymphocytes(CD3,CD5) fibroblast(vimentin),goblet cell(PAS with diastase with alcian blue), mast cells(CD11

●      Best corrected visual acuity (BCVA) 

●      Slit lamp examination:

i) AC reaction:Standard Uveitis Nomenclature (SUN Classification)

ii) Cataract state (LOCS)

iii) Bleb morphology assessment: IBAGS

·       Anterior segment optical coherence tomography (ASOCT)

Bleb characteristics evaluated would be-

      -Bleb wall thickness at - i) 12 O’ clock position

               ii) At area of greatest height

      -Bleb reflectivity would be evaluated throughout bleb area.

●      Ocular surface Disruption: by Tear Break Up Time (BUT) and keratometry

●      Complications during or after surgery including the requirement for Bleb needling.

●      Visual  fields examination  by Humphrey field analyzer 24-2/10-2 as required

●      Number of anti-glaucoma medications used

 

 

 

                                       STATISTICAL EVALUATION

SAMPLE SIZE: The study of Maheshwari D , et al in 2019 observed that mean intraocular pressure at 6 months in open angle glaucoma was 10.5 ± 2.6 and in angle closure glaucoma was 12 ± 3.8. Taking these values as reference, the minimum required sample size with 80% power of study and 5% level of significance is 74 patients in each study group. So total sample size taken is 150 (75 patients per group).

 

 

 

Formula used is:

For comparing mean of two groups

                     N>=2(standard deviation)2 *(Zα + Zβ)2

                                                   (mean difference)2​

        Where Zα is value of Z at two sided alpha error of 5% and Zβ is value of Z at power

of 80% and mean difference is difference in mean values of two groups.

Pooled standard deviation= Sqrt(((S1)2+(S2)2)/2)

          Where S1 is standard deviation of 1 group.

          And S2 is standard deviation of other group.

 

Calculations:

Pooled standard deviation=sqrt(((2.6)2+(3.8)2)/2) =3.25

N>=2(3.25)2 *(1.96 + .84)2 , (1.5)2​>=73.61=74(approx.)

 

STATISTICAL ANALYSIS

 Categorical variables will be presented in number and percentage (%) and continuous variables will be presented as mean ± SD and median.  Normality of data will be tested by Kolmogorov-Smirnov test. If the normality is rejected then non parametric test will be used.

Statistical tests will be applied as follows-

1.Quantitative variables will be compared using Unpaired t-test/Mann-Whitney Test (when the data sets were not normally distributed) between the two groups.

2.Qualitative variables will be compared using Chi-Square test /Fisher’s exact test.

A p value of <0.05 will be considered statistically significant.

The data will be entered in MS EXCEL spreadsheet and analysis will be done using Statistical Package for Social Sciences (SPSS) version 25.0.

Type of Study:  Prospective comparative study

 

 ETHICAL CONSIDERATIONS

●      Informed consent will be taken from each study subject

●      Confidentiality will be maintained for each study subject

●       Subjects will have freedom to opt out of study at any point of time

●       Prior approval of ethical committee of Maulana Azad Medical College will be taken prior to conduct of study

 

 

 


 

 


 
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