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CTRI Number  CTRI/2024/03/064868 [Registered on: 27/03/2024] Trial Registered Prospectively
Last Modified On: 20/03/2024
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Biological
Surgical/Anesthesia 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Study to assess the efficacy of Graft material for Myringoplasty between ttemporalis fascia vs Dehydrated Human Amniotic Membrane  
Scientific Title of Study   Comparative Study of Efficacy of Temporalis Fascia vs Dehydrated Human Amniotic Membrane as Graft Material in Myringoplasty- A randomized controlled trial”. 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Indranil Sen 
Designation  Professor 
Affiliation  College of medicine and Sagore Dutta Hospital  
Address  Department of OTORHINOLARYNGOLOGY College of Medicine and Sagore Dutta Hospital Kolkta 700058

North Twentyfour Parganas
WEST BENGAL
700058
India 
Phone  9749283857  
Fax    
Email  indranilsen.india@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Indranil Sen 
Designation  Professor 
Affiliation  College of medicine and Sagore Dutta Hospital  
Address  Department of OTORHINOLARYNGOLOGY College of Medicine and Sagore Dutta Hospital Kolkta 700058

North Twentyfour Parganas
WEST BENGAL
700058
India 
Phone  9749283857  
Fax    
Email  indranilsen.india@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Anup Kumar Das  
Designation  Assistant Professor 
Affiliation  College of Medicine and Sagore Dutta Hospital 
Address  Department of OTORHINOLARYNGOLOGY College of Medicine and Sagore Dutta Hospital Kolkta 700058

North Twentyfour Parganas
WEST BENGAL
700058
India 
Phone  6290853295  
Fax    
Email  anoopdas70@gmail.com  
 
Source of Monetary or Material Support  
College of Medicine and Sagore Dutta Hospital 578 B. T. Road, Kamarhati, Kolkata - 700058, West Bengal Kolkata 700058 
 
Primary Sponsor  
Name  College of Medicine and Sagore Dutta Hospital 
Address  578, B.T. Road. Kamarhati. Kolkata 700058 
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 Indranil Sen  College of Medicine and Sagore Dutta Hospital  578 B. T. Road. Kamarhati Kolkata 700058
North Twentyfour Parganas
WEST BENGAL 
9749283857

indranilsen.india@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
IEC College of Medicine And Sagore Dutta Hospital   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: H661||Chronic tubotympanic suppurative otitis media,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Myringoplasty using two different graft material  Myringoplasty is known to be done with different graft materials. in this study a comparative outcome analysis will be done between autologous temporalis fascia vs dehydrated human amniotic membrane as established wound healing graft 
 
Inclusion Criteria  
Age From  15.00 Day(s)
Age To  50.00 Day(s)
Gender  Both 
Details  (a) Patients aged 15 years to 50 years
(b)Patients having ‘Quiescent Mucosal type’ of Chronic Otitis media
 
 
ExclusionCriteria 
Details  (a) Patients having ‘Squamosal type’ of Chronic Otitis media
(b) Patients having ‘Mixed deafness’ or ‘Sensorineural’ deafness
(c) Patients having ossicular damage on examination under microscope (EUM)
(d) Patients having vestibular symptom
(e) Patients having any suggestive complication of otitis media
(f) Very low general condition/ severe medical disability/ unsound mental status
(g) Patients having persistent infective focus in ENT region, clinically
(h) Patients suspected to suffer from chronic specific infective/ Granulomatous diseases eg Tuberculosis, Leprosy etc.
(i) Non-cooperative patients
 
 
Method of Generating Random Sequence   Random Number Table 
Method of Concealment   Alternation 
Blinding/Masking   Participant and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Complete healing and functional recovery of Tympanic membrane   6-12 weeks  
 
Secondary Outcome  
Outcome  TimePoints 
Improvement of heariing and PQLI  six months to one year 
 
Target Sample Size   Total Sample Size="100"
Sample Size from India="100" 
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 4 
Date of First Enrollment (India)   15/04/2024 
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="2"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary  

Perforation of the Tympanic Membrane (TM) is a common complication of various types of pathologies of the middle ear, mostly infective in origin. A group of patients require plastic surgical repair of the TM perforation. The operative procedure involves the placement of some graft material as a template, upon which, the fresh epithelium grows to cover up the perforation and the healing is achieved. Experiments have been going on for the search of an ideal graft material for a long time. Various tissue materials e.g. perichondrium of the adjacent cartilages, vein graft, spilt thickness skin, cartilage (Homograft/ Allograft), dermal fat, Temporalis fascia and  synthetic materials like cigarette paper, silastic sheet, Gelfoam. Surgicel etc. have been tried by various research workers. Among these, the use of the Temporalis fascia is most popular and common. However, each and every graft material has its advantages and limitations. Recently, commercially available allograft materials such as Alloderm (Life Cell Corp., Branchburg, NJ) derived from donated skin from human cadavers has been used as an alternative to autologous tissue in efforts to reduce scarring, infection and pain, as well as operative time. Although, this material may provide a suitable grafting option, it’s acellular characteristic only serves as a scaffold or template for in-growth, which may limit its long-term success [1.6.9.11]. An important component of tissue engineering  (TE)  is the supporting matrix upon which cells and tissues grow, also known as the scaffold. Scaffolds must easily integrate with host tissue and provide an excellent environment for cell growth and differentiation. Most scaffold materials are naturally derived from mammalian tissues. The amniotic membrane (AM)  is considered an important potential source for scaffolding material. The AM represents the innermost layer of the placenta and is composed of a single epithelial layer, a thick basement membrane and an avascular stroma. The special structure and biological viability of the AM allows it to be an ideal candidate for creating scaffolds used in TE. Epithelial cells derived from the AM have the advantages of stem cells, yet are a more suitable source of cells for TE than stem cells. The extracellular matrix components of the basement membrane of the AM create an almost native scaffold for cell seeding in Tissue engineering. In addition, the Amniotic membrane has other biological properties , including anti-inflammatory, anti-microbial, anti-fibrosis, anti-scarring, as well as reasonable mechanical property and low immunogenicity [2.7.10.12.15.17].

Keeping the above properties of amniotic membrane in mind an ‘Experimental Study’ ‘is proposed to be conducted among patients attending the out-patients wing of Otorhinolaryngology Department of College of Medicine & Sagore Datta Hospital (COMSDH) and Bidhan Nagar State General Hospital (BNSGH- situated within a radius of 50 kms of COMSDH) to compare the efficacy of  Temporalis Fascia vs Dehydrated Human Amniotic Membrane as graft material in Myringoplasty.

The study will be conducted over a span of about 2years among subjects selected through proper inclusion and exclusion criteria. The objectives will be To study the effects of Myringoplasty for Tympanic Membrane Perforation with Temporalis Fascia Graft vis-à-vis Dehydrated Human Amniotic Membrane on the healing parameters of the operated patients & Comparative assessment of efficacy on the healing effects of the two different graft materials. Data will be collected as per pre-designed pro-forma and relevant investigations followed by definitive surgical management will be done.

After approval from the Technical Advisory Committee and the Institutional Ethics Committee, data collection and statistical analysis of the study will be done and published in due course.

 
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