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Effectiveness of acemannan in orabase and triamcinolone acetonide in orabase for treatment of aphthous ulceration

Effectiveness of acemannan in orabase and triamcinolone acetonide in orabase for treatment of aphthous ulceration

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20171013001
Enrollment
56
Registered
2017-10-13
Start date
2017-10-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Aphthous ulcer

Interventions

Experimental Drug,Active Comparator Drug
Acemannan in orabase,Triamcinolone acetonide in orabase
Topical application of 0.5% acemannan in orabase on the ulcer 3 times a day,Topical application of 0.1% acemannan in orabase on the ulcer 3 times a day

Sponsors

Faculty of Dentistry, Naresuan University
Lead Sponsor
Research Unit of Herbal Medicine and Natural Product for Dental Application&#44
Collaborator
Chulalongkorn Universit
Collaborator

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Willing to participate and signed the informed&#45;consent forms 2. Has 1&#45;3 aphthous ulcers of < 48 hours duration on nonkeratinized oral mucosa 3. Ulcer size is 2–10 mm in diameter 4. Healthy (not having systemic disease)

Exclusion criteria

Exclusion criteria: 1. History of allergies to aloe vera&#44; acemannan&#44;or triamcinolone in orabase 2. Previously treatment with topical triamcinolone acetonide in this aphthous ulcer 3. Pregnancy and/or lactation 4. Having oral bacteria/fungal/viral infections 5. Having systemic disease process which involved with aphthous ulceration or impaired wound healing such as ulcerative colitis&#44; Crohn’s disease&#44; Behcet’s syndrome&#44; or diabetes mellitus or anemia 6. Dental surgery within 2 weeks

Design outcomes

Primary

MeasureTime frame
Wound size reduction 2&#44; 5&#44; and 7 days after applied treatment Measurement and calculate the remaining wound area

Secondary

MeasureTime frame
Pain reduction 2&#44; 5&#44; and 7 days after applied treatment Visual Analog Scale (VAS)

Contacts

Public ContactSuwimon Jettanacheawchankit

Deparment of Oral Biology&#44; Faculty of Dentistry&#44; Naresuan University

suwimonj@nu.ac.th0818905254

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026