Topical Timolol for Superficial Infantile Hemangioma

Sponsor
Mahidol University (Other)
Overall Status
Unknown status
CT.gov ID
NCT01685398
Collaborator
(none)
46
1
2
33
1.4

Study Details

Study Description

Brief Summary

Infantile hemangioma (IH) is the most common benign vascular tumor in pediatric population. The characteristic natural history of this tumor is rapid growth in the first year of life and follows by spontaneous involution. However, it may cause cosmetic unacceptable. Early intervention in superficial IH may help to minimize the risk of residual aesthetic problems. Topical timolol, a non selective beta-blocker, is an emerging treatment which has been reported in efficacy and safety for the treatment of IH. However, the reported studies were case-series or small study. This study is a prospective double-blind,randomized-controlled study to evaluate the efficacy and safety of 0.5% timolol maleate solution for treatment in superficial IH. The patient will be treated with topical timolol for at least 6 months and instructed to 4 times daily apply 1-2 drop of timolol solution on the lesion and rub over the entire lesion with a finger. Photographs of the lesion will be taken at the baseline and every 1-month visit. Clinical evaluation of the treatment efficacy is carried out by 2 investigators independently to determine the change in lesion size and visual analogue scale of the lesion color. The main outcome is to evaluate the efficacy of 0.5% timolol maleate solution in treatment of infantile hemangioma compared to placebo.

Condition or Disease Intervention/Treatment Phase
  • Drug: 0.5% timolol maleate eye drop
  • Drug: Normal saline
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
46 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Treatment of Cutaneous Hemangioma of Infancy With Topical 0.5% Timolol Maleate Eye Drop Compared With Placebo in Pediatric Patients, Siriraj Hospital
Study Start Date :
Sep 1, 2012
Anticipated Primary Completion Date :
Jun 1, 2015
Anticipated Study Completion Date :
Jun 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: normal saline

normal saline 1-2 drops put on the hemangioma lesion 4 times a day and rub over the entire lesion with a finger

Drug: Normal saline
Other Names:
  • Saline
  • Experimental: 0.5% timolol maleate eye drop

    0.5% timolol maleate solution 1-2 drops put on the hemangioma lesion 4 times a day and rub over the entire lesion with a finger

    Drug: 0.5% timolol maleate eye drop

    Outcome Measures

    Primary Outcome Measures

    1. Efficacy of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma compared to placebo [6 months]

      Percent changes in visual analogue scale of the lesion color and global assessment scale of the lesion after treatment

    Secondary Outcome Measures

    1. Side effects of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma [6 months]

      The side effects of 0.5% timolol maleate solution include bradycardia, dizziness, irritant contact dermatitis, allergic contact dermatitis, fatigue, nausea, diarrhea,and insomnia. To determine the side effects, investigators will monitor the vital signs of the patients every follow-up visit and ask the caretakers about the side effects. Furthermore, every patients will receive the dairy to record the frequency of drug usage and side effects found.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 2 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patient who is less than 2 years

    • Patient who has been diagnosed with superficial infantile hemangioma

    • The tumor which has been in proliferative or plateau phase

    • There is no indication for systemic treatment

    • Informed consent is obtained from the parent of the patient

    Exclusion Criteria:
    • Patient who has the indication for systemic therapy

    • Patient who is treated by the other modality such as laser treatment

    • Patient who has underlying disease treated by beta blocker, corticosteroids, interferon, cyclophosphamide or vincristine

    • Patient who has history of hypersensitivity reaction to beta blocker, asthma, cardiac condition prove to heart block

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Faculty of Medicine Siriraj Hospital Mahidol University Bangkoknoi Bangkok Thailand 10700

    Sponsors and Collaborators

    • Mahidol University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mahidol University
    ClinicalTrials.gov Identifier:
    NCT01685398
    Other Study ID Numbers:
    • 088/2555(EC4)
    First Posted:
    Sep 14, 2012
    Last Update Posted:
    Nov 27, 2012
    Last Verified:
    Jun 1, 2012
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 27, 2012