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The efficacy of nail gutter method with topical timolol and topical timolol under occlusion for patients with epidermal growth factor receptor inhibitors induced paronychia: Single-blinded intrapatient randomized controlled study

Phase 2
Recruiting
Conditions
Cancer patients aged more than 18 years who received EGFR inhibitors therapy and have more than two paronychia/pyogenic granuloma of finger/nail that affect their everyday life.
EGFR inhibitor, PRIDE syndrome, paronychia/pyogenic granuloma
Registration Number
TCTR20221026003
Lead Sponsor
Faculty of Medicine Siriraj Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
56
Inclusion Criteria

1.Cancer patients aged more than 18 years who received EGFR inhibitors therapy
2. Patients have more than two paronychia/pyogenic granuloma of finger/nail (CTCAE paronychia grade 2 and 3) that affect their everyday life.

Exclusion Criteria

Patients with underlining diseases: asthma,COPD, arrhythmia,
Patients who have infected nail that lead to nail extraction.
Patients with neutropenia and thrombocytopenia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Response 8 weeks after primary intervention Complete response (CR), Partial response (PR), No response score (NR)
Secondary Outcome Measures
NameTimeMethod
SPOT score ,VAS,CTCAE paronychia grading within 8 weeks after primary intervention Doctor evaluate response
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