Systemic Propranolol for the Treatment of Paediatric Patients With Infantile Hemangiomas
- Registration Number
- NCT04651049
- Lead Sponsor
- Qilu Hospital of Shandong University
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 128
- IHs diagnosed by medical history and physical examination
- no previous treatment with other medications
- 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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Propranolol treatment group propranolol -
- Primary Outcome Measures
Name Time Method Change on the height of the patients at the beginning of the treatment, at the end of treatment and 2 years after the treatment we recorded the height of the patients in meters.
Change on the weight of the patients at the beginning of the treatment, at the end of treatment and 2 years after the treatment we recorded the weight of the patients in kilograms.
- Secondary Outcome Measures
Name Time Method
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