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Preliminary safety assessment of infantile hemangioma drug patch

Preliminary safety assessment of infantile hemangioma drug patch

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052763
Enrollment
Unknown
Registered
2021-11-05
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-08-16

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

Conditions

Infantile Hemangioma

Interventions

Group 1:Hemangioma Topical Drug
Group 2:Hemangioma Drug Patch

Sponsors

Shanghai Ninth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 0.5 Years

Inclusion criteria

Inclusion criteria: 1. Patients with untreated superficial infantile hemangioma in the proliferative stage; 2. Children younger than 6 months old; 3. Non-facial lesions; 4. The lesion area is less than 4cm^2, the height protruding from the skin surface is less than 3mm, and there is no ulcer, bleeding, infection, scar, etc. on the surface; 5. The family members of the children have informed and consented, and can cooperate with the inspection and follow-up required by the trial.

Exclusion criteria

Exclusion criteria: 1. Bronchial asthma, severe congenital heart disease; 2. The skin is allergic to ordinary tape; 3. Those who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale;

Countries

China

Contacts

Public ContactLin Xiaoxi
linxiaoxi@126.com+86 13701997136

Outcome results

None listed

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