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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04747275
Other study ID # STUDY00001385
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date January 18, 2021
Est. completion date November 1, 2021

Study information

Verified date September 2023
Source Children's Mercy Hospital Kansas City
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Children with levothyroxine (T21) have developmental delay and other functional gastrointestinal (GI) issues that may negatively affect L-T4 tolerability and absorption. For an age group unable to swallow tablets whole by mouth, tablets must be crushed and suspended in water, breast milk or formula for administration in order to treat children with hypothyroidism. For this age group, ease of administration may have a significant impact on compliance and ability to remain euthyroid. We propose that Tirosint-SOL® will be more favorably received due to ease of administration, improved tolerability and palatability, therefore leading to improved adherence when compared to L-T4 tablets.


Description:

Hypothyroidism is a common medical disorder in children with Trisomy 21 (T21). Treatment with oral tablet levothyroxine (L-T4) is primarily used to treat this condition. However, children with T21 have developmental delay and other functional gastrointestinal (GI) issues that may negatively affect L-T4 tolerability and absorption. For an age group unable to swallow tablets whole by mouth, tablets must be crushed and suspended in water, breast milk or formula for administration in order to treat children with hypothyroidism. For this age group, ease of administration may have a significant impact on compliance and ability to remain euthyroid. Until recently, there was no liquid preparation of L-T4 in the United States for use in children. Tirosint-SOL® (liquid stable L-T4) is now FDA-approved for use in children. The Investigator proposes that Tirosint-SOL® will be more favorably received due to ease of administration, improved tolerability and palatability, therefore leading to improved adherence when compared to L-T4 tablets.


Recruitment information / eligibility

Status Terminated
Enrollment 6
Est. completion date November 1, 2021
Est. primary completion date November 1, 2021
Accepts healthy volunteers No
Gender All
Age group 2 Months to 4 Years
Eligibility Inclusion Criteria: - Trisomy 21 children age 2 months to less than 5 years of age - Prior confirmed diagnosis of congenital or acquired hypothyroidism Exclusion Criteria: - Gestational age = 35 weeks, concomitant anticonvulsant medications, history of nonadherence with medication or medical visit schedule - Subjects must be able to take oral medication, no G-tube or parental fed subjects

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Liquid stable levothyroxine (L-T4) Tirosint-SOL
Investigation of tolerability, palatability, and adherence of liquid levothyroxine (L-T4) for 8 weeks.
Oral tablet levothyroxine (L-T4)
Investigation of tolerability, palatability, and adherence of maintained oral tablet levothyroxine (L-T4) for 8 weeks

Locations

Country Name City State
United States Children's Mercy Hospital Kansas City Missouri

Sponsors (1)

Lead Sponsor Collaborator
Children's Mercy Hospital Kansas City

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tolerability as Assessed by the CareCAT Tool Utilize medication tolerability questionnaire, Care Children's Acceptance Tool (CAT), to understand parental perceptions of liquid stable L-T4. 4 months
Secondary Adherence to Taking Study Medication Evaluate differences in compliance with liquid stable L-T4 compared to L-T4 tablet. Evaluated in percentage of days compliant. 4 months
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