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Efficacy of PDL laser and topical propranolol in treatment of infantile hemangioma.

Comparision of efficacy of combination PDL laser with topical propranolol and PDL laser alone in treatment of infantile hemangioma.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110137787N1
Enrollment
28
Registered
2012-01-08
Start date
2011-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Infantile Hemangioma.

Interventions

Intervention 1: Perform PDL laser(3 sessinns)with 4 weeks interval +daily application of topical propranolol by the patient up to 3 months. Intervention 2: PDL laser alone is performed (3 sessions wit
Treatment - Drugs
Treatment - Other
Perform PDL laser(3 sessinns)with 4 weeks interval +daily application of topical propranolol by the patient up to 3 months.
PDL laser alone is performed (3 sessions with 4 weeks interval)

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 2 Years

Inclusion criteria

Inclusion criteria: Inclusion crateria : 1-Hemangioma located in non-sensitive area(include nose-ear-eyelid-lips) 2-Patient compliance with study 3-No previous treatment(with systemic corticosteroids or other drugs) received in the last 3 months. 4-Patients shold not have any systemic involvement(congenital heart disease-renal disease) 5-Hemangioma in the proliferative phase of evolution(age<2 years). Exclusion crateria: 1-no response after 4 weeks of treatment 2-Allergic reaction to anyone of topical drugs. 3-Side effects of topical propranolol (e.g erythema,pruritus,inflamation......)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Efficacy of topical propranolol with PDL laser and PDL laser alone in treatment of infantile hemangioma. Timepoint: 0-4-8-12-16 weeks. Method of measurement: Evaluation and comparision of lesion photographs according to VAS(Visual Analogue Scale).

Secondary

MeasureTime frame
Improvement of overall health of patient. Timepoint: 4-8-12-16 weeks after initial treatment. Method of measurement: Patients parents.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mona Abdolreza

Razi Hospital

abdolreza@razi.tums.ac.ir+98 21556099513

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026