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Systemic Propranolol for the Treatment of Paediatric Patients With Infantile Hemangiomas

Influence of Systemic Propranolol Treatment on the Physical Development of Paediatric Patients With Infantile Hemangiomas

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04651049
Enrollment
128
Registered
2020-12-03
Start date
2010-07-15
Completion date
2020-02-10
Last updated
2020-12-03

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

Conditions

Infantile Haemangiomas

Brief summary

This is retrospective study. The patients treated with oral propranolol at a dose of 2.0 mg/kg per day. Growth parameters (height and weight) were measured at the beginning, the end of treatment and 2 years after treatment. The weight-for-age Z-score (WAZ), height-for-age Z-score (HAZ) and weight-for-height Z-score (WHZ) calculated by the WHO Anthro software were used to assess physical development, and the WHO Child Growth Standards were used as the standards.

Interventions

DRUGpropranolol

This retrospective study included 128 patients treated with oral propranolol at a dose of 2.0 mg/kg per day.

Sponsors

Qilu Hospital of Shandong University
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Weeks to 54 Weeks
Healthy volunteers
No

Inclusion criteria

* IHs diagnosed by medical history and physical examination * no previous treatment with other medications

Exclusion criteria

* a history or risk of asthma, reactive airway disease, impaired renal or liver function, heart defects or arrhythmia, hypotension and hypersensitivity to propranolol * Infants who did not adhere to the treatments or attend follow-up visits * Infants with other known risk factors for developmental delay or growth restriction, such as prematurity, small for gestational age, or other major congenital malformations, were also excluded * No other treatment was used during the oral propranolol course

Design outcomes

Primary

MeasureTime frameDescription
Change on the height of the patientsat the beginning of the treatment, at the end of treatment and 2 years after the treatmentwe recorded the height of the patients in meters.
Change on the weight of the patientsat the beginning of the treatment, at the end of treatment and 2 years after the treatmentwe recorded the weight of the patients in kilograms.

Outcome results

None listed

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