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Study of effect of dental gel in improving gum condition.

A DOUBLE BLIND PLACEBO CONTROLLED STUDY TO ASSESS THE EFFICACY OF ACACIA ARABICA PHYTOPHARMACEUTICAL GEL AS AN ADJUNCT IN TREATMENT AND QUALITY OF LIFE ENHANCEMENT OF PERIODONTITIS PATIENTS. - ACA

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/09/004013
Enrollment
50
Registered
2013-09-23
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: null- localised periodontitis

Interventions

Intervention1: Acacia Arabica: Phyto pharmaceutical drug used twice daily as local application in the affected area
about pea size gel for one tooth area
for 3 months. Control Intervention1: placebo: A placebo gel. used twice daily as local application in the affected area
for 3 months.

Sponsors

Dr Rameshwari Singhal
Lead Sponsor
Charak pharmaceuticals
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: • Subjects of age 18 years or older of either gender in good general health condition • Subjects with mild to moderate Periodontitis (pocket depth 4-6mm) • Patients willing to sign Informed Consent Form.

Exclusion criteria

Exclusion criteria: •History of tobacco chewing / smoking •Any known clinically significant hematological, endocrine disorders, hepatic or renal diseases, cardiovascular, cerebrovascular or psychiatric diseases likely to alter the treatment outcome, or could compromise the subjectâ??s participation in the trial •Subjects who used medication that would interfere with the efficacy and safety objectives of the trial or who were not stabilized on any concomitant medication (continuous use) during at least three months prior to randomization. •Patients who participate in other study protocols

Design outcomes

Primary

MeasureTime frame
Primary efficacy outcomes: â?¢ Gingival index- Loe and Silness â?¢ Bleeding Index- Ainamo and Bay â?¢ Plaque Index- Silness and Loe. â?¢ PPD (Probing Pocket Depth) using Florida probe â?¢ CAL (clinical attachment level) using Florida probe. Timepoint: at baseline and 3 months after drug delivery.

Secondary

MeasureTime frame
â?¢ Modified OHRQL instrumentTimepoint: Baseline & 3 months

Countries

India

Contacts

Public ContactDr Rameshwari Singhal

Chhattarpati Shahuji Maharaj medical University

rsinghal23@hotmail.com

Outcome results

None listed

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