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Usefulness of Kshara Taila in Plaque-induced Gingivitis

Efficacy of Kshara Taila in Plaque induced Gingivitis A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072013
Enrollment
60
Registered
2024-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: K051- Chronic gingivitis

Interventions

None listed

Sponsors

G J Patel Institute of Ayurvedic Studies & Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) An anticipated ability to attend the scheduled visits 2) Having plaque-induced gingivitis (ICD-10-CM Diagnosis Code K05.10)

Exclusion criteria

Exclusion criteria: 1) Participants contra-indicated for gandusha or kavalagraha 2) Less than 20 natural teeth 3) Participants who are pregnant or nursing. 4) A dental student or faculty or dental staff member. 5) Usage of fixed or removable orthodontic appliance 6) Clinical loss of periodontal ligament / attachment 7) Recent history of (within two weeks prior to examination), or ongoing, antibiotic therapy. 8) A need for immediate antimicrobial treatment for periodontitis. 9) Continuing use of anticoagulant medications 10) Dry mouth syndrome or significant food allergies. 11) Any dental procedures or oral prophylaxis within 15 days prior to examination 12) Presence of an intraoral soft tissue pathology 13) Smoking 14) Any significant medical condition that contributes to the development of dental plaque (like diabetes, cardiovascular diseases, autoimmune conditions etc) 15) Presence of major physical or mental limitation or restriction that prohibit the hygiene procedures used in the study protocol 16) Any other condition which in the opinion of the investigators places the participant at risk if they were to participate in the study.

Design outcomes

Primary

MeasureTime frame
Improvement in Bleeding on probing score (BOP), expressed in percentage.Timepoint: 8 days after treatment and 16 days after treatment

Secondary

MeasureTime frame
1) Modified Gingival Index 2) Modified Plaque ScoreTimepoint: 8 days after treatment and 16 days after treatment

Countries

India

Contacts

Public ContactVishnu Govind M

The CVM University

vimalben.panchani@cvmu.edu.in9898381314

Outcome results

None listed

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