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Gandoosha (Oral Oil Retention Procedure) safety & efficacy on oral hygiene indices in Orodental Health.

An evaluation of safety, Efficacy and Treatment Adherence of Gandoosha (Oral Oil Retention Procedure) on Orodental Health in apparently healthy adult population- An assessor blind exploratory Randomized Controlled Study - (CCRAS-Gandoosha)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098944
Enrollment
80
Registered
2025-12-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

None listed

Interventions

None listed

Sponsors

CENTRAL COUNCIL FOR RESEARCH IN AYURVEDIC SCIENCES Ministry of AYUSH, Government of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Apparently Healthy Adults of age group from 18 to 60 years of all genders 2.Apparently Healthy Adults with or without removable or fixed prostheses or fixed and removable orthodontic appliances will be included. 3.Poor orodental hygiene with Simplified Oral Hygiene Index (OHI-S)- 3 to 6

Exclusion criteria

Exclusion criteria: 1.Population with uncontrolled systemic comorbidities like DM, HTN, IHD from available reports & ongoing medication record 2.Population with significant orodental pathology 3.Oral carcinoma in situ. 4.Oral premalignant conditions like- Erythroplakia, leukoplakia, OSMF (Screened participants with cancerous, precancerous lesions will be referred to Tata Memorial Hospital for further evaluation and management) 5.Use of antibiotics and anti-inflammatory drugs in previous one month 6.History of mouth rinses, gels or chewing gums use, that contain antimicrobial agents in the preceding one month 7.Chronic users of tobacco products (for more than three years) in its various forms 8.Participants with a history of regular or recent inhalation of corticosteroids 9.Allergy to any ingredient used in the study 10.Oral pathology that is interfering with the conduction of Gandoosha procedure- like OA/RA of TM joint 11.Participants with already a habit of practicing Gandoosha with any liquid 12.Pregnant or lactating females 13.Participants with hampered cough reflex

Design outcomes

Primary

MeasureTime frame
1. Salivary Microbiome Profiles (Day 0 and Day 21) 2. Simplified Oral Hygiene Index (OHI-S) (Day 0 and Day 21)Timepoint: Day 0 and Day 21

Secondary

MeasureTime frame
1. Status of orodental health assessed on the basis of WHO Oral Health Assessment form- Adults 2. Change in existing orodental clinical signs and symptoms, if present (E.g.- tastelessness, halitosis, dental pain, sensitive tooth, mouth ulcers, gingival pain, bleeding etc.) 3. Safety profile assessed by incidence of AEs/ADRs 4. Treatment adherence will be assessed through the MARS-5 questionnaire.Timepoint: Day 0 and Day 21

Countries

India

Contacts

Public ContactDr R Govind Reddy

RRAP CENTRAL AYURVEDA RESEARCH INSTITUTE, Mumbai, CCRAS, MINISTRY OF AYUSH, GOVERNMENT OF INDIA

drrgreddy68@gmail.com02224947822

Outcome results

None listed

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