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
|
|
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
|
|
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
- What data in particular will be shared?
Response - All of the individual participant data collected during the trial, after de-identification.
- What additional supporting information will be shared?
Response - Study Protocol Response - Statistical Analysis Plan Response - Clinical Study Report
- Who will be able to view these files?
Response - Anyone
- For what types of analyses will this data be available?
Response - For individual participant data meta-analysis.
- By what mechanism will data be made available?
Response - Proposals should be directed to [sharonsarathomas@gmail.com].
- 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
- Any URL or additional information regarding plan/policy for sharing IPD?
Additional Information - NIL
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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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