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Effect of different discontinuation regimens of propranolol on relapse of infantile hemangiomas: a prospective randomized controlled study

Effect of different discontinuation regimens of propranolol on relapse of infantile hemangiomas: a prospective randomized controlled study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033415
Enrollment
Unknown
Registered
2020-05-31
Start date
2020-06-08
Completion date
Unknown
Last updated
2020-06-01

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

Conditions

infantile hemangioma

Interventions

A:discontinued propranolol directly from 1 month after the hemangioma reaches its maximum regression
B:discontinued propranolol directly from 3 months after the hemangioma reaches its maximum regression
C:discontinued propranolol gradually within 4 weeks from 1 month after the hemangioma reaches its maximum regression
D:discontinued propranolol gradually within 4 weeks from 3 months after the hemangioma reaches its maximum regression

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 0.5 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as infantile hemangioma according to the criteria of the International Society for the Study of Vascular Anomalies; 2. Patients younger than 6 months with infantile hemangiomas in proliferative phase; 3. Patients with no previous treatment; 4. Patients guardians who give their informed consents, and are willing to accept the trail and follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications of propranolol, such as cardiac disease (cardiac dysplasia, bradycardia, arrhythmia, heart failure, and pulmonary hypertension), pulmonary disease (asthma, and pneumonia), hypothyroidism, Raynauds syndrome, pheochromocytoma, and abnormal liver and kidney function; 2. Patients who are allergic to ß-adrenergic receptor antagonist; 3. Patients who are participating in other clinical trails.

Design outcomes

Primary

MeasureTime frame
minor relapse;

Secondary

MeasureTime frame
major relapse;adverse events;

Countries

China

Contacts

Public ContactHuo Ran

Shandong Provincial Hospital

huoran@medmail.com.cn+86 15168889001

Outcome results

None listed

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