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CTRI Number  CTRI/2025/06/088758 [Registered on: 12/06/2025] Trial Registered Prospectively
Last Modified On: 29/05/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Dentistry 
Study Design  Other 
Public Title of Study   A study on comparing healing after root end microscopic surgery using a natural blood healing gel with or without light therapy 
Scientific Title of Study   Investigating Periapical Healing Following Endodontic Microsurgery Using Autologous Grafts With or Without Photobiomodulation A Randomized Controlled Study  
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Sharon Sara Thomas 
Designation  Junior Resident  
Affiliation  King Georges Medical University 
Address  Department of Conservative Dentistry and Endodontics, Faculty of Dental Sciences, King Georges Medical University Lucknow UTTAR PRADESH 226003 India

Lucknow
UTTAR PRADESH
226003
India 
Phone  09497881094  
Fax    
Email  sharonsarathomas@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Vijay Kumar Shakya 
Designation  Professor 
Affiliation  King Georges Medical University 
Address  Department of Conservative Dentistry and Endodontics, Faculty of Dental Sciences, King Georges Medical University Lucknow UTTAR PRADESH 226003 India

Lucknow
UTTAR PRADESH
226003
India 
Phone  9140230667  
Fax    
Email  dr.vijay.shakya@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Rakesh Kumar Yadav 
Designation  Professor 
Affiliation  King Georges Medical University 
Address  Department of Conservative Dentistry and Endodontics, Faculty of Dental Sciences, King Georges Medical University Lucknow UTTAR PRADESH 226003 India

Lucknow
UTTAR PRADESH
226003
India 
Phone  9415281156  
Fax    
Email  rakeshanita10@yahoo.in  
 
Source of Monetary or Material Support  
Department of Conservative Dentistry & Endodontics , King Georges Medical University Lucknow, Uttar Pradesh, India Pin code-226003 
 
Primary Sponsor  
Name  NA 
Address  NA 
Type of Sponsor  Other [] 
 
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 Sharon Sara Thomas  Faculty of Dental Sciences  1st Floor, Department of Conservative Dentistry & Endodontics, Old Dental Building, Faculty of Dental Sciences, King Georges Medical University Lucknow UTTAR PRADESH
Lucknow
UTTAR PRADESH 
09497881094

sharonsarathomas@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
King Georges Medical University , Institutional Ethics Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  , (1) ICD-10 Condition: K046||Periapical abscess with sinus, (2) ICD-10 Condition: K047||Periapical abscess without sinus, (3) ICD-10 Condition: K048||Radicular cyst, (4) ICD-10 Condition: K049||Other and unspecified diseases ofpulp and periapical tissues,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Photobiomodulation   Photobiomodulation (808nm, 100 mW, and 4J/cm2 ) applications will be made in the immediate postoperative period and 24 hours after endodontic microsurgery and PRF placement with an irradiation time of 150 s over the periapical tissues of involved tooth.  
Comparator Agent  Without Photobiomodulation  After Endodontic Microsurgery and PRF placement,laser tip simulation will be given without activation over the periapical tissues of the involved tooth in the control group in the immediate postoperative period and 24 hrs later. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  40.00 Year(s)
Gender  Both 
Details  1. All patients within 18–40 years of age who will give a written consent to participate in the study
2. Single rooted, maxillary anterior teeth.
3. Teeth with peri apical radiolucency indicated for surgery.
4. Patient should be of sufficient mental capacity and be in possession of all essential information.
5. Patients who are not on any medication affecting periapical healing. (corticosteroids, chemotherapeutic agents, non-steroidal anti-inflammatory drugs (NSAIDs), antibiotics, anticoagulants and drugs which reduce osteoblastic activity).
 
 
ExclusionCriteria 
Details  1. Patients who did not give their consent for participating in the study.
2. Patients having insufficient motivation to report back for follow up visits.
3. Patients with any systemic diseases like diabetes mellitus, hypertension, hepatitis, Human immunodeficiency virus, bone disorders, auto-immune disorders.
4. Surgical retreatment cases.
5. Patients with malignant tumors or undergoing chemotherapy/radiotherapy.
6. Pregnant females.
7. Patients with periodontally compromised teeth.
 
 
Method of Generating Random Sequence   Random Number Table 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Clinical Assessment of soft tissue healing and postoperative pain.
Radiographic Assessment of healing. 
Clinical Assessment to be done at 24 hrs, 3 days and 7 days postoperatively
Radiographic Assessment to be done at 1 month and every 3 month interval upto 1 year 
 
Secondary Outcome  
Outcome  TimePoints 
Assessing soft tissue healing and increase in microvascualture using Ultrasonography with Color Doppler and 3D bone fill using CBCT  Ultrasonography with Color Doppler to be done at 3,6, 9 and 12 months.CBCT Assessment to be done at 6 months and 1 year 
 
Target Sample Size   Total Sample Size="28"
Sample Size from India="28" 
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)   01/07/2025 
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 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 - YES
  1. What data in particular will be shared?
    Response - All of the individual participant data collected during the trial, after de-identification.

  2. What additional supporting information will be shared?
    Response -  Study Protocol
    Response -  Statistical Analysis Plan
    Response - Clinical Study Report

  3. Who will be able to view these files?
    Response - Anyone

  4. For what types of analyses will this data be available?
    Response - For individual participant data meta-analysis.

  5. By what mechanism will data be made available?
    Response - Proposals should be directed to [sharonsarathomas@gmail.com].

  6. For how long will this data be available start date provided 02-07-2025 and end date provided 02-07-2026?
    Response (Others) -  upto the publication and it depends upon the policy of publishing journal whether they allow to share data or not

  7. Any URL or additional information regarding plan/policy for sharing IPD? 
    Additional Information - NIL
Brief Summary  
Primary Purpose of the Study
The primary purpose of this randomized, double-blinded clinical study is to evaluate and compare the periapical healing outcomes following Endodontic Microsurgery and Platelet-Rich Fibrin (PRF) placement , with and without adjunctive Photobiomodulation Therapy (PBMT), using clinical, radiographic, ultrasonographic (with color Doppler), and CBCT imaging methods over a 12-month follow-up period.. This study seeks to determine whether the combination of regenerative [ using PRF] and adjunctive therapies [using PBMT] enhances tissue regeneration, reduces inflammation, and improves overall clinical outcomes compared to conventional treatment approaches

Endodontic microsurgery (EMS) has shown high success rates in managing persistent periapical pathosis, especially with advancements in microsurgical techniques, imaging modalities like CBCT and Ultrasonography with Color Doppler, and the use of regenerative biomaterials such as Platelet-Rich Fibrin (PRF). PRF enhances healing by releasing a concentrated mix of growth factors that promote tissue regeneration and angiogenesis. Photobiomodulation Therapy (PBMT), also known as low-level laser therapy, has demonstrated additional regenerative potential by stimulating cellular proliferation, improving microcirculation, and reducing postoperative inflammation and pain. Combining PRF with PBMT may synergistically enhance periapical healing following EMS by accelerating tissue repair and improving bone regeneration outcomes. This study seeks to investigate whether adjunctive PBMT offers significant benefits over PRF alone in post-surgical periapical healing assessed through clinical, radiographic, ultrasonographic (with color Doppler), and CBCT evaluations.

MATERIAL AND METHODS:
The present study will be conducted in the Department of Conservative Dentistry and Endodontics, Faculty of Dental Science, King George’s Medical University, Lucknow in collaboration with Department of
Radiodiagnosis, King George’s Medical University, Lucknow.  The study aims to include patients of age group 18 to 40 years with radiographic evidence of periapical lesion indicated for surgery and who will give a written consent and adhere in the inclusion criteria of the study. They  will be categorized into two groups based on use of photo biomodulation therapy.
Surgery under magnification followed by placement of PRF will be done in all patients. Following which PBMT will be applied in study group and laser simulation without activation will be done in control group. Clinical , radiographical evaluation will be done to evaluate the periapical healing at required intervals. Ultrasonographic with color doppler study  and CBCT evaluations will also be done at required intervals to assess neo angiogenesis and three dimensional bone fill respectively.
Data obtained will be statistically analysed. Any changes deemed in the interest to the study will be done accordingly.


 
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