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A NEW HERBAL TURMERIC BASED MATERIAL TO REPLACE LOST BONE AROUND THE TEETH IN PATIENTS

A NEOTERIC APPROACH TO REGENERATION OF INTRABONY DEFECTS BY USING CURCUMIN GEL AS A BONE REGENERATIVE MATERIAL VERSUS BIOACTIVE SYNTHETIC BONE GRAFT: A RANDOMIZED CONTROLLED CLINICAL TRIAL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010492
Enrollment
60
Registered
2017-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K053- Chronic periodontitis Health Condition 2: null- LOCALIZED OR GENERALIZED PERIODONTITIS

Interventions

Intervention1: CURCUMIN GEL : 1% curcumin gel will be placed in the site of bone defect. the dose or amount of gel to be placed will depend on the extent of defect or bone loss. this gel will be give

Sponsors

RAJARAJESWARI DENTAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients willing to undergo regenerative treatment for intrabony defects. 2. Presence of intrabony defect with a clinical probing pocket depth of >= 6mm, with radiographic evidence. 3. Systemically healthy patients 4. Patients who have not been on any medications within the last 6 months which may alter the periodontal status. 5. Patients with no history of allergy to materials and drugs used or prescribed in this study 6. Patients who are willing to follow oral hygiene practices after phase I therapy.

Exclusion criteria

Exclusion criteria: 1. Patients unwilling to participate in the study. 2. Smokers and alcoholic patients. 3. Pregnant and lactating mothers. 4. Patients who have undergone periodontal treatment within the last 1 year 5. Patients with plaque index >1 and who are unwilling to follow oral hygiene practices after phase I therapy.

Design outcomes

Primary

MeasureTime frame
to clinically and radiographically measure amount of bone regenerationTimepoint: 0, 3, 6, 9 months

Secondary

MeasureTime frame
reduction in all the clinical parameters measured except clinical attachment level where a gain is expectedTimepoint: 0, 3, 6 and 9 months

Countries

India

Contacts

Public ContactDR C KAVITA

RAJARAJESWARI DENTAL COLLEGE & HOSPITAL

kripalkrishna@yahoo.com9632597504

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026