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An evaluation of the assistant efficacy of periodontal treatment for the oral erosion lichen planus and the post-treatment

An evaluation of the assistant efficacy of periodontal treatment for the oral erosion lichen planus and the post-treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13004128
Enrollment
Unknown
Registered
2013-04-30
Start date
2012-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Oral lichen planus

Interventions

Group B:Blockage of triamcinolone acetonide injection
Group A:oral hygiene and Blockage of triamcinolone acetonide injection

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 1860 years old; 2. Subject decided independently to participate in the study and sign informed consent; 3. Histopathologically and clinically proved oral erosive OLP; 4. Single erosin lesion,and the lesion size not exceeding 1 square centimeter; 5. Disease-process exceeding 2 months; 6. Negative reaction to pregnancy test in women; 7. Result of a physiccal examination is normal.

Exclusion criteria

Exclusion criteria: 1. Aggressive and generalized periodontitis or other periodontitis as a manifeststion of system diseases; 2. History of allergies to dexamethasone or a known history of serious drug hypersensitivities; 3. Those with other severe oral mucous diseases; 4. Those taking immunopotentiating or immunosuppressive agents during the previous 3 months; those having topical treatment of lichen planus within a week; 5. Those with severe systemic diseases or abnormal hepatic or renal function test; a history of hepatitis C; 6. Pregnancy or intention of pregnancy or lactation or use of contraceptives of steroid hormone recently; 7. History of psychiatric disorders; 8. Lichenoid disease induced by amalgam or other drugs.

Design outcomes

Primary

MeasureTime frame
Pain level;Lesion size;Erosive healing rate;

Countries

China

Contacts

Public ContactHongmei Zhou

West China Hospital of Stomatology, Sichuan University

acomnet@126.com+86 28 85503480

Outcome results

None listed

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