Clinical Trials Directory

Trials / Unknown

UnknownNCT06050863

Local Delivery of Silk Fibroin and Chlorhexidine

A Comparative Evaluation of Subgingivally Delivered Chlorhexidine, Silk Fibroin and Combination of Fibroin and Chlorhexidine as Local Drug Delivery in Periodontitis - A Randomized Control Trial

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
15 (estimated)
Sponsor
Krishnadevaraya College of Dental Sciences & Hospital · Academic / Other
Sex
All
Age
30 Years – 50 Years
Healthy volunteers
Accepted

Summary

The current study is a prospective randomised split mouth study to evaluate the effect of Silk fibroin as drug delivery system while simultaneously assessing the efficacy of silk fibroin in comparison to chlorhexidine.

Detailed description

Fifteen healthy individuals satisfying the inclusion and exclusion criteria were recruited for the study. A detailed, thorough medical and dental history was obtained and each patient was subjected to comprehensive clinical and radiological examination. All patients were informed about the nature of the study, procedure involved, potential benefits and risks associated with procedure and written informed consent were obtained from all patients.All the patients underwent scaling and root planing. Following randomization, the site will be assigned to one of the three study groups. 1. Group I (SRP+ Silk Fibroin) 2. Group II (SRP+ Chlorhexidine) 3. Group III (SRP+ Combination of Fibroin and Chlorhexidine) Periodotal pack was placed and patient was recalled after 21days, 1 month and 3 month for the follow up.

Conditions

Interventions

TypeNameDescription
BIOLOGICALsilk fibroinsilk fibroin extracted from bombyx mori silk worm is processed in laboratory to form silk fibroin films
DRUGChlorhexidinchlorhexidine is used
BIOLOGICALcombination of silk fibroin and chlorhexidinecombination of silk fibroin and chlorhexidine is used

Timeline

Start date
2023-11-01
Primary completion
2024-06-01
Completion
2024-07-01
First posted
2023-09-22
Last updated
2023-09-22

Source: ClinicalTrials.gov record NCT06050863. Inclusion in this directory is not an endorsement.