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Aged Garlic extract on minor RecurrentAphthous Stomatitis

Comparative Evaluation of Aged Garlic extract and Triamcinolone Acetonide in minor Recurrent Aphthous Stomatitis. A randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075470
Enrollment
60
Registered
2024-10-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: K120- Recurrent oral aphthae

Interventions

Intervention1: Aged Garlic Extract: GROUP A Four capsule each containing Aged garlic extract of 600mg. Take two capsules with a meal two times a day. (BD) (Total Dose-2,400mg,per day) For 2 weeks.

Sponsors

DrRutuja Kadam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with minor recurrent aphthous stomatitis, Presenting with single or multiple minor aphthous ulcers of more than 48 hours duration, Ulcers must be in locations easily accessible for evaluation and treatment, such as the buccal mucosa, labial mucosa, floor of the mouth, or tongue. Diagnosed with RAS according to the original criteria of Lehner (1968).

Exclusion criteria

Exclusion criteria: History of allergies to garlic and triamcinolone acetonide, Patients with recurrent aphthous ulcer major and recurrent herpetiform ulcer, Patient already undergoing treatment for recurrent aphthous Stomatitis, Pregnant and lactating females, Patients on medication for any reason (oral problems, systemic Problems), Patients with any systemic problem or syndrome, Ulcers as a manifestation of systemic diseases.

Design outcomes

Primary

MeasureTime frame
USS ulcerative severity score, (OHIS) Oral health impact scoreTimepoint: Patient will be recalled at the end of 4 th day, 7 th day,14 th day • Post treatment follow up will be done on monthly basis for three months (30 th day, 60 th day, 90 th day) • Evaluation of the following parameters will be done on each visit 1.Ulcer Severity Score(USS) 2.Oral health impact score(OHIS) 3.Adverse effects if any - If Recurrence occurs, standard treatment (Triamcinolone Acetonide 0.1% buccal paste) will be provided.

Secondary

MeasureTime frame
Side effects of intervention, if anyTimepoint: Patient will be recalled at the end of 4th day, 7th day,14th day. Post treatment follow up will be done on monthly basis for three months (30th day, 60th day, 90th day). Evaluation of the following parameters will be done on each visit 1.Ulcer Severity Score(USS) 2.Oral health impact score(OHIS) 3.Adverse effects if any - If Recurrence occurs, standard treatment (Triamcinolone Acetonide 0.1% buccal paste) will be provided

Countries

India

Contacts

Public ContactRUTUJA KADAM

Government Dental College And Hospital Nagpur

kalaskarashita@gmail.com8550928585

Outcome results

None listed

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