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Natural Berry Extract Treatment of Hemangiomas (Pediaberry)

Primary Purpose

Hemangioma

Status
Terminated
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
PediaBerry
Sponsored by
Gayle Gordillo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemangioma focused on measuring miR126, Pediaberry

Eligibility Criteria

1 Month - 19 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children with hemangiomas ≤ 4 months and 2 weeks of corrected gestational age
  • Hemangioma size ≥ 1 cm diameter

Exclusion Criteria:

  • Children with hemangiomas that threaten the life of the child or development of vital structures.
  • Children who are breast feeding and mother is taking beta blocker medication
  • Children with previously treated hemangiomas
  • Congenital hemangiomas - cannot distinguish between rapidly involuting and non-involuting congenital hemangiomas
  • Hemangiomas located in the perineal/diapering area - product will get contaminated or wiped off with diapering
  • Children with food allergies to blueberries or any other kind of berry
  • Legal guardian unable to provide informed consent

Sites / Locations

  • Riley Hospital for Children
  • Nationwide Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Pediaberry group

Placebo

Arm Description

PediaBerry™ is a proprietary blend powdered berry extracts

Placebo: powdered sugar plus McCormick Color from Nature Food Colors Berry and Sky Blue powdered food color (https://www.mccormick.com/spices-and-flavors/extracts-and-food-colors/food-colors/color-from-nature-assorted-food-color ).

Outcomes

Primary Outcome Measures

Decreased Hemangioma Size
Decrease in the size of hemangioma > 50%

Secondary Outcome Measures

Decreased urinary micro RNA 126 levels
Urinary micro RNA 126 levels are analyzed using quantitative polymerase chain reactions

Full Information

First Posted
June 24, 2019
Last Updated
October 18, 2023
Sponsor
Gayle Gordillo
Collaborators
National Institute of General Medical Sciences (NIGMS), National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT04020419
Brief Title
Natural Berry Extract Treatment of Hemangiomas
Acronym
Pediaberry
Official Title
Natural Berry Extract Treatment of Hemangiomas
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Terminated
Why Stopped
Study ending early due to program transferring to another site.
Study Start Date
December 1, 2020 (Actual)
Primary Completion Date
May 24, 2023 (Actual)
Study Completion Date
May 24, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Gayle Gordillo
Collaborators
National Institute of General Medical Sciences (NIGMS), National Institutes of Health (NIH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a prospective, randomized, double-blind, placebo-controlled parallel group study evaluating the use of PediaBerry for the treatment of hemangiomas in infants ≤ 4 months of corrected gestation age over a 6-month treatment period. Subjects will be followed to age 18 months. A total of 44 subjects will be PediaBerry group and 22 subjects in the placebo control group.
Detailed Description
PediaBerry™ is a proprietary blend of powdered berry extracts. Placebo: powdered sugar plus McCormick Color from Nature Food Colors Berry and Sky Blue powdered food color (https://www.mccormick.com/spices-and-flavors/extracts-and-food-colors/food-colors/color-from-nature-assorted-food-color ). Cream vehicle is mixed with PediaBerry™ or placebo at the time of application.Children will receive once daily topical and oral gavage dosing of PediaBerry or placebo. The first study visit will take place within 2 weeks of subject recruitment. The subject enrollment, consenting and randomization will occur as study visit #0 and will occur at Riley Children's Hospital or Nationwide Children's Hospital. Data collection will be the same at all study visits starting with study visit #1 until the completion of the study. The first dose of PediaBerry™ or placebo will be administered prior to completion of study visit #1, and will also be given at study visits #2-6. Study visits #2-6 will occur monthly study visits until the subject completes 6 months of treatment.Subjects will be weighed and treatment doses adjusted accordingly. Study visits #7-11 to watch for signs of rebound hemangioma proliferation will occur every other month until age 12 months and then at age 15 and 18 months. Urine samples, photos and caliper measurements will occur at each study visit. Some subjects may have less than 11 study visits depending on the age at the time of subject enrollment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemangioma
Keywords
miR126, Pediaberry

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Model Description
pilot study to determine effect size for possible FDA phase I/II trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
investigational pharmacy will have access to randomization schemes and will package study drug from bulk supplies. All other study team members and participants are blinded.
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pediaberry group
Arm Type
Experimental
Arm Description
PediaBerry™ is a proprietary blend powdered berry extracts
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo: powdered sugar plus McCormick Color from Nature Food Colors Berry and Sky Blue powdered food color (https://www.mccormick.com/spices-and-flavors/extracts-and-food-colors/food-colors/color-from-nature-assorted-food-color ).
Intervention Type
Drug
Intervention Name(s)
PediaBerry
Other Intervention Name(s)
placebo
Intervention Description
PediaBerry or placebo will be mixed with a cream vehicle for topical administration or with water for oral administration
Primary Outcome Measure Information:
Title
Decreased Hemangioma Size
Description
Decrease in the size of hemangioma > 50%
Time Frame
6 month treatment period
Secondary Outcome Measure Information:
Title
Decreased urinary micro RNA 126 levels
Description
Urinary micro RNA 126 levels are analyzed using quantitative polymerase chain reactions
Time Frame
6 month treatment period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
19 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children with hemangiomas ≤ 4 months and 2 weeks of corrected gestational age Hemangioma size ≥ 1 cm diameter Exclusion Criteria: Children with hemangiomas that threaten the life of the child or development of vital structures. Children who are breast feeding and mother is taking beta blocker medication Children with previously treated hemangiomas Congenital hemangiomas - cannot distinguish between rapidly involuting and non-involuting congenital hemangiomas Hemangiomas located in the perineal/diapering area - product will get contaminated or wiped off with diapering Children with food allergies to blueberries or any other kind of berry Legal guardian unable to provide informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gayle Gordillo, MD
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Riley Hospital for Children
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Nationwide Children's Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Natural Berry Extract Treatment of Hemangiomas

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