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The Application of carbon dioxide Laser in the Treatment of Oral Mucosal homogeneous Leukoplakia

The Application of carbon dioxide Laser in the Treatment of Oral Mucosal homogeneous Leukoplakia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120281
Enrollment
Unknown
Registered
2026-03-11
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Oral leukoplakia

Interventions

Single-arm Cohort:CO2 laser therapy: continuous pulse mode, power 10-15W, mucosa-head distance 15-20mm, head focal length 125mm, laser exposure time 20s, spot diameter 0.3mm, energy 4244 J/cm^2, resec
postoperative use of chlorhexidine acetate to prevent infection, compound chamomile lidocaine gel for pain relief.

Sponsors

The Third Affiliated Hospital of Air Force Medical University of the Chinese People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with clinically diagnosed oral leukoplakia presenting predominantly as white plaques, and pathologically confirmed as oral leukoplakia without epithelial dysplasia by histopathological examination. 2. Lesions with well-defined borders and an area no larger than 30×30 mm^2. 3. Age between 18 and 70 years old, with normal mental and intellectual status. 4. Normal vital signs (blood pressure, pulse, respiration), and normal results in routine examinations including blood routine, blood glucose, coagulation function, hepatitis B, hepatitis C, syphilis, and HIV tests.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women. 2. Patients with hypersensitivity to both articaine and lidocaine. 3. Patients with severe systemic diseases (e.g., cardiovascular diseases, diabetes mellitus, liver diseases, renal insufficiency, tumors, etc.). 4. Patients taking long-term oral contraceptives or steroids. 5. Patients who are not suitable for surgery.

Design outcomes

Primary

MeasureTime frame
Treatment response rate;

Secondary

MeasureTime frame
Toluidine blue and fluorescence staining;Recurrence rate after treatment;Histopathological assessment (inflammatory and proliferative markers);

Countries

China

Contacts

Public ContactWang Yuanyuan

The Third Affiliated Hospital of Air Force Medical University, PLA

1194704956@qq.com+86 150 2925 5303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026