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Safety and efficacy of topical Tanshinone gel treatment of infantile hemangioma: a prospective, multicenter, self-controlled clinical trial.

Safety and efficacy of topical Tanshinone gel treatment of infantile hemangioma: a prospective, multicenter, self-controlled clinical trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017926
Enrollment
Unknown
Registered
2018-08-22
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-08-27

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

Conditions

Infantile hemangiomas

Interventions

experimental group: topical Tanshinone gel treatment
self-controlled group:No treatment (observation)

Sponsors

Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: 1) Patients that were diagnosed as superficial infantile hemangioma according to classification and naming criteria for vascular diseases of the International Classification of Vascular Abnormalities (ISSVA); 2) The number of systemic lesion is =2; 3) The hemangioma is in a proliferative phase (the child is younger than 6 months, or more than 6 months, but less than 12 months, and the tumor still grows significantly in the near future), regardless of gender; 4) Never received other treatments; 5) Parents fully understand that this is a clinical trial and voluntarily sign the informed consent form of the legal guardian to cooperate with the referral within the prescribed time.

Exclusion criteria

Exclusion criteria: 1) Children with a history of allergies to any of the ingredients to be used; 2) There are ulcers, infections, eczema in the lesions, and it is impossible to use topical drugs; 3) Children with a history of serious congenital diseases and severe heart disease; 4) Children with clinical significant abnormality of electrocardiogram, chest X-ray, ultrasound, liver and kidney; 5) According to the researcher's judgment, the subject is not credible or poorly compliant.

Design outcomes

Primary

MeasureTime frame
wether the leision is completely removed;

Secondary

MeasureTime frame
the thickness and blood flow of the leision;Changes in appearance before and after treatment of lesions;the color of leisions;

Countries

China

Contacts

Public ContactYeming Wu

Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

wuymsh@163.com+86 13003178888

Outcome results

None listed

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