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Topical Timolol for Superficial Infantile Hemangioma

Treatment of Cutaneous Hemangioma of Infancy With Topical 0.5% Timolol Maleate Eye Drop Compared With Placebo in Pediatric Patients, Siriraj Hospital

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01685398
Enrollment
48
Registered
2012-09-14
Start date
2012-09-30
Completion date
2023-03-31
Last updated
2023-09-21

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

Conditions

Hemangioma

Brief summary

Infantile hemangioma (IH) is the most common benign vascular tumor in pediatric population. The characteristic natural history of this tumor is rapid growth in the first year of life and follows by spontaneous involution. However, it may cause cosmetic unacceptable. Early intervention in superficial IH may help to minimize the risk of residual aesthetic problems. Topical timolol, a non selective beta-blocker, is an emerging treatment which has been reported in efficacy and safety for the treatment of IH. However, the reported studies were case-series or small study. This study is a prospective double-blind,randomized-controlled study to evaluate the efficacy and safety of 0.5% timolol maleate solution for treatment in superficial IH. The patient will be treated with topical timolol for at least 6 months and instructed to 4 times daily apply 1-2 drop of timolol solution on the lesion and rub over the entire lesion with a finger. Photographs of the lesion will be taken at the baseline and every 1-month visit. Clinical evaluation of the treatment efficacy is carried out by 2 investigators independently to determine the change in lesion size and visual analogue scale of the lesion color. The main outcome is to evaluate the efficacy of 0.5% timolol maleate solution in treatment of infantile hemangioma compared to placebo.

Interventions

DRUG0.5% timolol maleate eye drop
DRUGNormal saline

Sponsors

Mahidol University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
No minimum to 2 Years
Healthy volunteers
Yes

Inclusion criteria

* Patient who is less than 2 years * Patient who has been diagnosed with superficial infantile hemangioma * The tumor which has been in proliferative or plateau phase * There is no indication for systemic treatment * Informed consent is obtained from the parent of the patient

Exclusion criteria

* Patient who has the indication for systemic therapy * Patient who is treated by the other modality such as laser treatment * Patient who has underlying disease treated by beta blocker, corticosteroids, interferon, cyclophosphamide or vincristine * Patient who has history of hypersensitivity reaction to beta blocker, asthma, cardiac condition prove to heart block

Design outcomes

Primary

MeasureTime frameDescription
Efficacy of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma compared to placebo6 monthsPercent changes in visual analogue scale of the lesion color and global assessment scale of the lesion after treatment

Secondary

MeasureTime frameDescription
Side effects of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma6 monthsThe side effects of 0.5% timolol maleate solution include bradycardia, dizziness, irritant contact dermatitis, allergic contact dermatitis, fatigue, nausea, diarrhea,and insomnia. To determine the side effects, investigators will monitor the vital signs of the patients every follow-up visit and ask the caretakers about the side effects. Furthermore, every patients will receive the dairy to record the frequency of drug usage and side effects found.

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026