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Effectiveness of topical timolol compared with oral propranolol for infant hemangiomas

Comparison of Topical Timolol with Oral Propranolol in Terms of Efficacy and Treatment Outcomes for Infantile Hemangiomas: A Randomized Controlled Trial.

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000236392
Enrollment
40
Registered
2026-02-24
Start date
2026-03-18
Completion date
2026-04-18
Last updated
2026-03-02

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

Conditions

None listed

Brief summary

This study will help us by comparing the efficacy of topical timolol with oral propranolol in treating the infantile hemangiomas, as oral propranolol has been used traditionally for its treatment but it has more side effects and requires monitoring for hypotension and hypoglycemia. topical timolol is established as a much safer alternative. So we want to find if it is also comparable with regarding to its efficacy and outcomes. This study will provide valuable insights for healthcare providers, policymakers, and families, ultimately contributing to the development of patient-centred care

Interventions

The pediatric population with simple superficial infantile hemangioma will be treated in two groups. One group will be treated with topical timolol applied thrice a day, Group A: Topical timolol (0.5% eye drops) 1 drop per cm2 applied topically 3 thrice a day to the hemangioma for 4 months. Monthly follow ups will be done for first 4 months to evaluate the response of the treatment in both groups. Contact details of individuals will be obtained after consent for adherence to the follow ups.

Sponsors

King edward Medical University Lahore
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
1 Months to 12 Months
Healthy volunteers
No

Inclusion criteria

o Infants aged 1 to 12 months. o Diagnosed with superficial infantile hemangiomas with no complications requiring treatment. o Parental consent obtained

Exclusion criteria

o Infants with deep hemangiomas. o Infants with contraindications to beta-blockers (e.g., bradycardia, hypotension, asthma). o Infants with significant comorbidities that could affect the study outcomes

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 14, 2026