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CTRI Number  CTRI/2024/09/074346 [Registered on: 25/09/2024] Trial Registered Prospectively
Last Modified On: 10/09/2024
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Dentistry 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Evaluating the effectiveness of a novel bilayer film loaded with ornidazole and ofloxacin for the treatment of patients with moderate periodontitis - A randomized controlled trial 
Scientific Title of Study   Evaluation of a novel bilayer film loaded with ornidazole and ofloxacin for the treatment of patients with moderate periodontitis – 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  Dr Shruti Karvekar 
Designation  Faculty 
Affiliation  KAHERs KLE V.K Institute of Dental Sciences 
Address  KAHERs KLE V.K Institute of Dental Sciences, Nehru Nagar, Belagavi, Karnataka, India 590010

Belgaum
KARNATAKA
590010
India 
Phone  9986155460  
Fax    
Email  shruti.karvekar@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Shruti Karvekar 
Designation  Faculty 
Affiliation  KAHERs KLE V.K Institute of Dental Sciences 
Address  KAHERs KLE V.K Institute of Dental Sciences, Nehru Nagar, Belagavi, Karnataka, India 590010


KARNATAKA
590010
India 
Phone  9986155460  
Fax    
Email  shruti.karvekar@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Shruti Karvekar 
Designation  Faculty 
Affiliation  KAHERs KLE V.K Institute of Dental Sciences 
Address  KAHERs KLE V.K Institute of Dental Sciences, Nehru Nagar, Belagavi, Karnataka, India 590010


KARNATAKA
590010
India 
Phone  9986155460  
Fax    
Email  shruti.karvekar@gmail.com  
 
Source of Monetary or Material Support  
KAHER’s Research and Development Cell, Belagavi, Karnataka, India 590010 
 
Primary Sponsor  
Name  KAHER’s Research and Development Cell 
Address  KAHERs KLE V.K Institute of Dental Sciences, Nehru Nagar, Belagavi, Karnataka, India 590010 
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 Shruti Karvekar  KAHERs KLE V.K Institute of Dental Sciences  Room no. 9, Department of Periodontics, KAHERs KLE V.K Institute of Dental Sciences, Nehru Nagar, Belagavi, Karnataka, India 590010
Belgaum
KARNATAKA 
9986155460

shruti.karvekar@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Research and Ethics Committee KLE VKIDS  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: K053||Chronic periodontitis,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Bilayer film  Patients will receive full mouth supra and subgingival scaling and root planing followed by the subgingival delivery of the bilayer film in moderate to deep pockets. Duration: Baseline and 7 days 
Comparator Agent  SRP  Patients will receive only full mouth supra and subgingival scaling and root planing. Duration: Baseline and 7 days 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  Patients with a pocket depth of 5–7 mm in at least three non-adjacent sites in different quadrants of the mouth
Systemically healthy controls
Cooperative patients who could be motivated for further oral hygiene instructions
Patients with ≥20 teeth
Patients who consented to participate in the study
 
 
ExclusionCriteria 
Details  Patients on antibiotic therapy from the past 1 month
Pregnant or lactating women
Smokers or patients with any habit history
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Case Record Numbers 
Blinding/Masking   Participant and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Gingival Index by Loe and Silness, Plaque index by Silness and Loe, Pocket Probing Depth and Clinical Attachment Loss
 
Baseline, 1 week, 1 month
 
 
Secondary Outcome  
Outcome  TimePoints 
Colony forming units/ml  Baseline, 1 week, 1 month
 
 
Target Sample Size   Total Sample Size="18"
Sample Size from India="18" 
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)   26/09/2024 
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="1"
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  

• Periodontitis is the most common and a major public health problem due to its high prevalence (25% to 55%) worldwide, and also because it leads to tooth loss, and degrades the quality of life.  Periodontal therapy includes both mechanical and chemical therapeutic agents which help in the reduction or elimination of microbial biofilm.1

• Conventional plaque control methods like ultrasonic scaling and root planing [SRP] has reduced effectiveness because it lacks accessibility to micro-organisms in the sub-gingival environment. The administrations of systemic antimicrobial drugs have failed to achieve the adequate concentration at the required sites and its frequent usage has led to bacterial resistance.1 

• Local drug delivery systems prove beneficial because of their ability to reach the base of the periodontal pocket and also cause sustained release of short dose of drug over a long period of time. It has shown promising results in mild and moderate chronic periodontitis. Among these, bilayer film incorporated with antimicrobial agents is a promising approach to treat periodontitis due to its muco-adhesivity, biodegradability, biocompatibility, non-toxicity, controllability of drug release, and easy insertion into the target place.2

• Bilayer films are the drug delivery system that contain more than one active pharmaceutical agent in a double layered polymeric film. They are gaining preference over single layer films as they offer a combination of unique properties of all substrates, which is often advantageous. Bilayer films can be made as mucoadhesive films by using mucoadhesive polymers with the added advantage of incorporating a sustained drug release layer and an immediate drug release.3

• Ofloxacin is a fluorinated carboxy quinolone exhibiting a marked bactericidal effect by inhibiting DNA gyrase. In vitro studies on bactericidal activity have suggested that ofloxacin is likely to be the most useful drug in the treatment and prevention of periodontitis. It is a synthetic broad-spectrum antimicrobial agent for oral administration.4

• Ornidazole is an antibiotic used for the treatment of anaerobic infections. As anaerobic bacteria are believed to be the predominant causative factor in periodontitis it is used in the treatment of chronic periodontitis. It acts by inhibiting DNA synthesis. It works on the principle that inactive form passively diffuses into cell where it is activated by chemical reduction. The nitro group gets reduced into anion radicals which causes oxidation of DNA leading to strand breakage and cell death. Hence, it has both antimicrobial and mutagenic effects.5

 

There have been no reported clinical studies using a bilayer film containing ofloxacin, ornidazole and as a local drug delivery agent in periodontitis. Hence, the present study aims at formulation, optimization and evaluation of a bilayer film combining ofloxacin and ornidazole for the treatment of patients diagnosed with moderate periodontitis.

 
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