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Clinical investigation of the effect of anchor toothpaste as compared to regular toothpaste on plaque and gingival status.

A randomnized double blinded parallel controlled clinical trial to compare the plaque removal efficacy and gingival health of Anchor toothpaste as compared to regular toothpaste (Colgate dental cream among adult population in Dharwad

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2008/091/000020
Enrollment
80
Registered
2008-06-09
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: Y992- Volunteer activity

Interventions

Intervention1: a) Anchor anti-plaque and anti-gingivatis toothpaste: Brushing twice a day for 4 weeks Control Intervention1: Colgate Tooth paste: Brushing twice a day for 4 weeks

Sponsors

ANCHOR HEALTH AND BEAUTY CARE PRODUCTS MUMBAI
Lead Sponsor
SDM College of Dental Sciences Hospital Dharwad Karnataka
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Signed Informed Consent Form 2. Good General Health 3. Male and female subjects, aged 13-70, inclusive 4. At least 24 scorable teeth free of large restorations or dental prosthetic crowns. 5. Available for the entire duration of the study. 6. Clinical evidence of tendency to form plaque on teeth and mild gingivitis

Exclusion criteria

Exclusion criteria: 1. Presence of orthodontic appliances or more than one incisor with a prosthetic crown or veneer. 2. Tumors or significant pathology of the soft or hard tissues of the oral cavity. 3. Moderate or advanced periodontal disease. 4. Participation in any other clinical study or panel test or completion of clinical studies in the one month prior to the start of this study. 5. Pregnant or breast feeding women. 6. History of allergies to triclosan. Allergies to dentifrice products, personal care products or their ingredients. 7. Antibiotic or steroid therapy in the preceding month.

Design outcomes

Primary

MeasureTime frame
plaque status as assessed by Tureskey-Gilmore-Glickman modification of Quigley Hein Plaque IndexTimepoint: Baseline, 2 weeks and 4 weeks

Secondary

MeasureTime frame
Gingival status will be assessed by Loe and Sileness IndexTimepoint: Baseline, 2 weeks and 4 weeks

Countries

India

Contacts

Public ContactDr K V V Prasad
kakarlap@hotmail.com0836-2468142

Outcome results

None listed

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