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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

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

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20221026003
Enrollment
56
Registered
2022-10-26
Start date
2022-10-25
Completion date
Unknown
Last updated
2026-08-03

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

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

Interventions

Apply nail gutter with topical 0.5% timolol bid,Apply only topical 0.5% timolol bid
Active Comparator Drug,Active Comparator Drug
Nail gutter method plus topical 0.5% timolol bid,topical 0.5% timolol bid alone

Sponsors

Faculty of Medicine Siriraj Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Response 8 weeks after primary intervention Complete response (CR), Partial response (PR), No response score (NR)

Secondary

MeasureTime frame
SPOT score ,VAS,CTCAE paronychia grading within 8 weeks after primary intervention Doctor evaluate response

Countries

Thailand

Contacts

Public ContactLeena Chularojanamontri

Faculty of Medicine, Mahidol University

leenajim@gmail.com0818345132

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026