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Topical Timolol for Superficial Infantile Hemangioma

Primary Purpose

Hemangioma

Status
Completed
Phase
Phase 3
Locations
Thailand
Study Type
Interventional
Intervention
0.5% timolol maleate eye drop
Normal saline
Sponsored by
Mahidol University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemangioma

Eligibility Criteria

undefined - 2 Years (Child)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Faculty of Medicine Siriraj Hospital Mahidol University

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

normal saline

0.5% timolol maleate eye drop

Arm Description

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

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

Outcomes

Primary Outcome Measures

Efficacy of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma compared to placebo
Percent changes in visual analogue scale of the lesion color and global assessment scale of the lesion after treatment

Secondary Outcome Measures

Side effects of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma
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.

Full Information

First Posted
September 5, 2012
Last Updated
September 20, 2023
Sponsor
Mahidol University
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1. Study Identification

Unique Protocol Identification Number
NCT01685398
Brief Title
Topical Timolol for Superficial Infantile Hemangioma
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 Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
September 2012 (Actual)
Primary Completion Date
March 2023 (Actual)
Study Completion Date
March 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mahidol University

4. Oversight

Data Monitoring Committee
No

5. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemangioma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
normal saline
Arm Type
Placebo Comparator
Arm Description
normal saline 1-2 drops put on the hemangioma lesion 4 times a day and rub over the entire lesion with a finger
Arm Title
0.5% timolol maleate eye drop
Arm Type
Experimental
Arm Description
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
Intervention Type
Drug
Intervention Name(s)
0.5% timolol maleate eye drop
Intervention Type
Drug
Intervention Name(s)
Normal saline
Other Intervention Name(s)
Saline
Primary Outcome Measure Information:
Title
Efficacy of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma compared to placebo
Description
Percent changes in visual analogue scale of the lesion color and global assessment scale of the lesion after treatment
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Side effects of the topical 0.5% timolol maleate solution in treatment of infantile hemangioma
Description
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.
Time Frame
6 months

10. Eligibility

Sex
All
Maximum Age & Unit of Time
2 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Facility Information:
Facility Name
Faculty of Medicine Siriraj Hospital Mahidol University
City
Bangkoknoi
State/Province
Bangkok
ZIP/Postal Code
10700
Country
Thailand

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Topical Timolol for Superficial Infantile Hemangioma

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