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Efficacy of Herbal Dentifrice in Treatment of Chronic Periodontitis

NCT06043687 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2024-10-08

No results posted yet for this study

Summary

The study will be a single center, longitudinal prospective, triple blind (investigators, patients and statistician), randomized design. After informed consent, a target population of about 75 healthy adult volunteers with periodontitis will be included in the study. Patients will be randomized and categorized into three experimental groups each containing 25 patients. The randomization process will be carried out by use of sequentially numbered opaque sealed envelopes (SNOSE method).The recording of all the soft tissues data plaque index, gingival index, the modified sulcus bleeding index and the periodontal probing depth and clinical attachment level will be carried out at baseline, 4 weeks, 8 weeks, 12 weeks and will be maintained till 24 weeks for efficacy and safety evaluation.

Conditions

  • Chronic Periodontitis

Interventions

DRUG

Dentifrice Paste

Scaling and Root planing followed by dentifrice usage

Sponsors & Collaborators

  • Jasberry Healthcare Pvt. Ltd

    collaborator UNKNOWN

  • Dr. D. Y. Patil Dental College & Hospital

    lead OTHER

Principal Investigators

  • Dharmarajan Gopalakrishnan, MDS, PhD · Dr. D Y Patil Dental College and Hospital, Pimpri, Pune

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-01
Primary Completion
2023-10-15
Completion
2023-12-15

Countries

  • India

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06043687 on ClinicalTrials.gov