Thyroid Hormones Treatment in Asthma Exacerbation (THINAS)
Primary Purpose
Asthma
Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
IV thyroxin
Placebo
Sponsored by

About this trial
This is an interventional treatment trial for Asthma focused on measuring asthma, thyroid hormones, treatment, asthma exacerbation
Eligibility Criteria
Inclusion Criteria:
- 18 years of age or older
- Known Asthma
- The exacerbation is defined as moderate or severe.
- Not currently enrolled as an active participant in another clinical trial of a medical therapy or device.
- The patient or first degree family relative (in cases where the patient is intubated) has authorized his/her consent to participate in this trial. The patient will be asked to give his consent only after initial bronchodilator therapy
Exclusion Criteria:
- 60 years of age or older
- Known thyroid disorders
- Subject where thyrotoxicosis is suspected
- Known heart disease
- Heart rate > 140
Sites / Locations
- Rambam health care campus
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
IV thyroxin
control IV saline
Arm Description
IV thyroxin
Placebo
Outcomes
Primary Outcome Measures
time to normalization of PEF (peak expiratory flow)
The primary endpoint is the time to return of the PEF rate to normal values or personal base line.
Secondary Outcome Measures
Length of stay
• Length of stay (in cases of hospitalization in the internal medicine departments) or length of intubation (in cases of hospitalization in the MICU).
Time to oxygenation
Time to oxygen saturation > 95% (while breathing spontaneously and without oxygen supplements)
heart rate
Time to normalization of heart rate
respiratory rate
Time to normalization of respiratory rate
Full Information
NCT ID
NCT02086799
First Posted
February 11, 2014
Last Updated
July 29, 2014
Sponsor
Rambam Health Care Campus
1. Study Identification
Unique Protocol Identification Number
NCT02086799
Brief Title
Thyroid Hormones Treatment in Asthma Exacerbation
Acronym
THINAS
Official Title
Is There a Role for Thyroid Hormones Treatment in the Set-up of Acute Moderate to Severe Asthma Exacerbation
Study Type
Interventional
2. Study Status
Record Verification Date
July 2014
Overall Recruitment Status
Unknown status
Study Start Date
July 2014 (undefined)
Primary Completion Date
July 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rambam Health Care Campus
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will explore whether supplementation with thyroid hormones in the set-up of asthma exacerbation could improve the clinical outcomes.
The study will include adults admitted to Rambam health care campus for moderate to severe Asthma exacerbation.
The study is a prospective, randomized, double-blind, placebo-controlled, clinical trial. Patients will be randomized on admission to receive treatment with intra-venous thyroxine (100mcg once on admission and additional 100mcg after 12 hours) or placebo. The study treatment will be given only after the initial bronchodilator therapy, oxygen and informed consent are given. The primary endpoint is the time to return of the peak expiratory flow (PEF) rate to normal values or personal base line.
Detailed Description
Study population: The study will include adults admitted to Internal Medicine B (IMB) department, Internal Medicine H (IMH) department or medical intensive care unit (MICU) in Rambam-Health Care Campus for moderate to severe Asthma exacerbation. The severity of the exacerbation will be based on several acceptable clinical and laboratory criteria, including breathless, alertness, pulse rate, respiratory rate, partial pressure of oxygen in arterial blood (PaO2), partial pressure of carbon dioxide in arterial blood (PaCO2), oxygen saturation, peak expiratory flow (PEF). Study protocol: The study is a prospective, randomized, double-blind, placebo-controlled, clinical trial. Patients will be randomized on admission to receive treatment with intra-venous thyroxine (100mcg once on admission and additional 100mcg after 12 hours) or placebo. The study treatment will be given only after the initial bronchodilator therapy, oxygen and informed consent are given. The primary endpoint is the time to return of the PEF rate to normal values or personal base line. PEF rates will be examined first after initial bronchodilator therapy and then, every 8 hours.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
asthma, thyroid hormones, treatment, asthma exacerbation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
IV thyroxin
Arm Type
Experimental
Arm Description
IV thyroxin
Arm Title
control IV saline
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
IV thyroxin
Other Intervention Name(s)
elthyroxin, thyroxin, euthrux
Intervention Description
Patients will receive treatment with intra-venous thyroxine 100mcg once on admission and additional 100mcg after 12 hours.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
saline
Intervention Description
Patients will receive treatment with normal saline 100ml once on admission and additional 100ml after 12 hours
Primary Outcome Measure Information:
Title
time to normalization of PEF (peak expiratory flow)
Description
The primary endpoint is the time to return of the PEF rate to normal values or personal base line.
Time Frame
one week
Secondary Outcome Measure Information:
Title
Length of stay
Description
• Length of stay (in cases of hospitalization in the internal medicine departments) or length of intubation (in cases of hospitalization in the MICU).
Time Frame
one week
Title
Time to oxygenation
Description
Time to oxygen saturation > 95% (while breathing spontaneously and without oxygen supplements)
Time Frame
one week
Title
heart rate
Description
Time to normalization of heart rate
Time Frame
one week
Title
respiratory rate
Description
Time to normalization of respiratory rate
Time Frame
one week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years of age or older
Known Asthma
The exacerbation is defined as moderate or severe.
Not currently enrolled as an active participant in another clinical trial of a medical therapy or device.
The patient or first degree family relative (in cases where the patient is intubated) has authorized his/her consent to participate in this trial. The patient will be asked to give his consent only after initial bronchodilator therapy
Exclusion Criteria:
60 years of age or older
Known thyroid disorders
Subject where thyrotoxicosis is suspected
Known heart disease
Heart rate > 140
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
gidon berger, MD
Phone
972 502061166
Email
g_berger@rambam.health.gov.il
First Name & Middle Initial & Last Name or Official Title & Degree
nizar andria, MD
Phone
972 502062851
Email
nizar.andria@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zaher S Azzam, prof.
Organizational Affiliation
Rambam Health Care Campus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rambam health care campus
City
Haifa
ZIP/Postal Code
31096
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
gidon berger, MD
Phone
972 502061166
Email
g_berger@rambam.health.gov.il
12. IPD Sharing Statement
Learn more about this trial
Thyroid Hormones Treatment in Asthma Exacerbation
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