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A cohort study for relationship between treatment timeline and skin lesions of Superficial Infantile Hemangiomas

A cohort study for relationship between treatment timeline and skin lesions of Superficial Infantile Hemangiomas

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019177
Enrollment
Unknown
Registered
2018-10-30
Start date
2018-11-01
Completion date
Unknown
Last updated
2018-11-05

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

Conditions

Infantile Hemangioma

Interventions

Early stage Proliferation:0.5% Timolol Maleate
Late stage Proliferation:0.5% Timolol Maleate

Sponsors

Shanghai Ninth People's Hospital, Shanghai Jiaotong University School Of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were diagnosed with Infantile Hemangioma according to ISSVA diagnostic criteria; 2. Patients with superficial Infantile Hemangiomas presented to Shanghai Ninth People's Hospital during the time period of July to December, 2018. (Patients under 2 months' age were included in early stage proliferation group, patients aged over 2 months and under 1 year old were included in late stage proliferation group.) 3. Untreated lesion; 4. Lesions without ulceration, atrophy, bleeding, etc. 5. Willing to cooperate with treatment.

Exclusion criteria

Exclusion criteria: 1. Those with severe immune deficiency or congenital diseases; 2. Patients participating in other clinical trials or recieving other treatments; 3. Patients who have beta blocker drug allergies.

Design outcomes

Primary

MeasureTime frame
VAS;

Countries

China

Contacts

Public ContactXiaoxi Lin

Shanghai Ninth People's Hospital, Shanghai Jiaotong University School Of Medicine

linxx1007@sh9hospital.org+86 13701997136

Outcome results

None listed

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