Skip to content

Oral Propranolol Versus Fractional Carbon Dioxide CO2 Laser Assisted Delivery of Topical Timolol for Treatment of Infantile Hemangioma

Oral Propranolol Versus Fractional Carbon Dioxide CO2 Laser Assisted Delivery of Topical Timolol for Treatment of Infantile Hemangioma; A Randomized Controlled Comparative Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07560332
Enrollment
30
Registered
2026-05-01
Start date
2025-01-01
Completion date
2026-01-01
Last updated
2026-05-01

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

Conditions

Infantile Hemangioma (IH)

Keywords

propranolol, timolol, carbon dioxide laser, infantile hemangioma

Brief summary

To assess and compare the efficacy of systemic beta-blocker therapy with the efficacy and safety of fractional carbon dioxide laser-assisted delivery of a topical beta-blocker solution in the treatment of infantile hemangioma.

Interventions

oral propranolol is given daily in a dose of 1 to 2 mgékg daily for 3 months

DEVICEFractional CO2 laser with topical timolol

Weekly sessions were performed followed by application of timolol daily

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Months to 12 Years
Healthy volunteers
No

Inclusion criteria

, aged 1 month to 12 years \- presenting with superficial, deep, mixed, or proliferating IH.

Exclusion criteria

* other cutaneous or systemic infections * chronic systemic diseases * known allergy to topical timolol maleate * contraindications to laser or beta-blocker therapy * IH involving mucosal or perimucosal sites * and a history of adverse reactions to laser therapy or keloid tendency.

Design outcomes

Primary

MeasureTime frame
Improvement of global assessment score of infantile hemangioma3 months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026