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Efficacy and Safety of Different Initial Doses of Oral Propranolol in the Treatment of Ulcerated Infantile Hemangioma

RecruitingPhase 2, Phase 3Ages any - 1 YearAllWest China Hospital
NCT06798363 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The main objective of this study was to determine the efficacy of different doses of propranolol in the treatment of ulcerattion infantile hemangioma (IH).

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. all patients with ulcer IH; 2. children with ulcer IH treated with propranolol. Exclusion Criteria: 1\) children with ulcer IH who received other therapeutic interventions were excluded; 2) Children whose families refused to participate in the study; 3) patients with contraindications to oral propranolol, such as allergy to propranolol, severe bradycardia and bronchial asthma; 4) children lost to follow-up during oral propranolol treatment; 5) children unable to oral propranolol or continue to oral propranolol due to other reasons. \-
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What it tests

  • propranolol
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Where

3 sites
West China Hospital of Sichuan University
Chengdu, China
Sichuan Women and Children's Hospital
Chengdu, China
West China Second University Hospital of Sichuan University
Chengdu, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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