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A preliminary, nonrandomized, controlled study on the efficacy of personalized treatment for pigmentary mass of conjunctiva

A preliminary, nonrandomized, controlled study on the efficacy of personalized treatment for pigmentary mass of conjunctiva

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119784
Enrollment
Unknown
Registered
2026-03-03
Start date
2025-01-15
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Conjunctival pigmented masses

Interventions

conjunctival nevus:Follow-up (no malignancy)/local use of immunomodulators (partial malignancy)
primary acquired melanosis:Follow-up (no malignancy)/local use of immunomodulators (partial malignancy)
conjunctival melanoma(T3d-T4,Lymph node/systemic metastasis):Immunomodulator/Proton therapy/Targeted therapy (with BRAF mutation) /PD-1 therapy (without BRAF mutation)
conjunctival melanoma(T3a-T3c,N0M0):Immunomodulator/Targeted therapy (with BRAF mutation) /PD-1 therapy (without BRAF mutation)

Sponsors

Eye & ENT hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Different types and stages of conjunctival pigmented lesions;

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating women; 2.Patients who cannot cooperate with diagnosis and treatment: patients with intellectual disability and mental illness; 3.Patients who have received immunotherapy/targeted/radiation-related treatment for conjunctival tumors in the past; 4.Patients with autoimmune diseases; 5.Patients with a history of organ transplantation and currently taking immunosuppressants; 6.People with abnormal cardiopulmonary function and liver and kidney function; 7.People who are known to be allergic to BRAF inhibitors and MEK inhibitors;

Design outcomes

Primary

MeasureTime frame
tumor range;tumor recurrence;metastasis;patient survival;

Secondary

MeasureTime frame
Ocular surface inflammation and discomfort;Hematological changes;Intraocular change;

Countries

China

Contacts

Public ContactQian Jiang

Eye & ENT hospital of Fudan University

jiang.qian@fdeent.org+86 138 0183 5100

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026