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CTRI Number  CTRI/2026/02/103730 [Registered on: 12/02/2026] Trial Registered Prospectively
Last Modified On: 12/02/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Dentistry 
Study Design  Randomized, Parallel Group, Multiple Arm Trial 
Public Title of Study   Evaluation of different graft materials in gum repositioning surgery for the treatment of multiple gum recession in upper teeth 
Scientific Title of Study   Comparative evaluation of Acellular Dermal matrix, Titanium Platelet Rich Fibrin and Connective Tissue Graft using Zucchellis modification of Coronally Advanced Flap technique in the management of multiple adjacent Cairo’s RT1 Marginal Tissue Recession in maxilla: A Randomized Clinical Trial 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  NANEPALLI SAI TEJA 
Designation  Resident 
Affiliation  Army Dental Centre Research and Referral 
Address  Department of Periodontology Army Dental Centre (Research and Referral) Delhi Cantt

New Delhi
DELHI
110010
India 
Phone  7036876341  
Fax    
Email  saiteja6279@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr(Col) T Prasanth 
Designation  Head of Department 
Affiliation  Army Dental Centre Research and Referral 
Address  Department of Periodontology Army Dental Centre (Research and Referral) Delhi Cantt

New Delhi
DELHI
110010
India 
Phone  8284851155  
Fax    
Email  tprasanthavin@gmail.com  
 
Details of Contact Person
Public Query
 
Name  NANEPALLI SAI TEJA 
Designation  Resident 
Affiliation  Army Dental Centre Research and Referral 
Address  Department of Periodontology Army Dental Centre (Research and Referral) Delhi Cantt

New Delhi
DELHI
110010
India 
Phone  7036876341  
Fax    
Email  saiteja6279@gmail.com  
 
Source of Monetary or Material Support  
Army Dental Centre (Research & Referral) Delhi Cantt-110010 
 
Primary Sponsor  
Name  Army Dental Centre (Research and Referral) Delhi Cantt 
Address  Army Dental Centre (Research & Referral) Delhi Cantt-110010 
Type of Sponsor  Research institution and hospital 
 
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 NANEPALLI SAI TEJA  Army Dental Centre (Research and Referral)   Department of Periodontology/ 1C Wing/ Room no 209
New Delhi
DELHI 
7036876341

saiteja6279@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Army dental centre R and R  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: K060||Gingival recession,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Acellular Dermal matrix  Comparative evaluation of Acellular Dermal matrix, Titanium Platelet Rich Fibrin and Connective Tissue Graft using Zucchellis modification of Coronally Advanced Flap technique in the management of multiple adjacent Cairo’s RT1 Marginal Tissue Recession in maxilla 
Comparator Agent  Connective Tissue Graft   Comparative evaluation of Acellular Dermal matrix, Titanium Platelet Rich Fibrin and Connective Tissue Graft using Zucchellis modification of Coronally Advanced Flap technique in the management of multiple adjacent Cairo’s RT1 Marginal Tissue Recession in maxilla 
Intervention  Titanium Platelet Rich Fibrin   Comparative evaluation of Acellular Dermal matrix, Titanium Platelet Rich Fibrin and Connective Tissue Graft using Zucchellis modification of Coronally Advanced Flap technique in the management of multiple adjacent Cairo’s RT1 Marginal Tissue Recession in maxilla 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  1.Patients with ASA-1 Physical Status Classification
2. Multiple adjacent Cairo’s RT1 MTR on maxillary anterior teeth or premolars
3. Intact papilla on the mesial and distal aspect of the involved tooth
4. No surgical periodontal therapy in last 1 year on the involved site 
 
ExclusionCriteria 
Details  1. Smokers and chewers of tobacco
2. Teeth with mobility or root caries
3. Non Carious Cervical Lesions (NCCL)
4. Pregnant and lactating women
5. Malposed teeth
6. Systemically compromised patients 
 
Method of Generating Random Sequence   Coin toss, Lottery, toss of dice, shuffling cards etc 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Complete Root Coverage (CRC)
 
Baseline, 3 months, 6 months
 
 
Secondary Outcome  
Outcome  TimePoints 
1. Gingival Recession Height (RH)
2. Recession Width (RW)
3. Mean Root Coverage (MRC)
4. Width of Keratinized Gingiva (WKG)
5. Clinical Attachment Level (CAL) 
Baseline, 3 months, 6 months 
 
Target Sample Size   Total Sample Size="21"
Sample Size from India="21" 
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   N/A 
Date of First Enrollment (India)   27/02/2026 
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="6"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
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   In this study iam comparing percentage of root coverage that could be achieved by using coronally advanced flap technique with Acellular dermal matrix , Titanium platelet rich fibrin and connective tissue graft which is considered as gold standard till now. Patients will be enrolled based on inclusion and exclusion criteria.Procedures will be carried under aseptic conditions.All the measurements will be taken at baseline, 3 months, 6 months post operatively and will be subjected to statistical analysis. 
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