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Research on the Treatment of Oral Leukoplakia with Tretinoin Tablets

Research on the Treatment of Oral Leukoplakia with Tretinoin Tablets

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126022
Enrollment
Unknown
Registered
2026-06-02
Start date
2026-06-02
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

oral leukoplakia

Interventions

High-concentration topical tretinoin tablets group:High-concentration topical tretinoin tablets
Oral tretinoin tablets group:Oral tretinoin tablets
Low-concentration topical tretinoin tablets group:Low-concentration topical tretinoin tablets

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Histopathologically confirmed diagnosis of oral leukoplakia; 2.Age 18 years or older; 3.No use of retinoid drugs within the past 3 months; 4.Agreement to participate in the study and provision of signed informed consent;

Exclusion criteria

Exclusion criteria: 1.Pregnant or breastfeeding women, or individuals planning pregnancy within the next 2 years; 2.Patients with hepatic or renal insufficiency or severe systemic diseases; 3.Individuals with a known allergy to retinoid drugs; 4.Histopathological diagnosis of severe dysplasia, carcinoma in situ, or microinvasive carcinoma;

Design outcomes

Primary

MeasureTime frame
Objective Response Rate for Oral Leukoplakia;

Secondary

MeasureTime frame
Changes in subjective assessment before and after treatment;

Countries

China

Contacts

Public ContactYu Zhou

West China Hospital of Stomatology, Sichuan University

812471898@qq.com+86 28 8550 3503

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026