Measurement of Natriuretic Hormone Peptides in Exacerbation of Asthma (acute asthma)
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Purpose
The investigators hypothesize that there is a statistically significant decrease of Natriuretic Hormone Peptides (NHPs) in subjects with asthma exacerbation compared to levels following treatment of an exacerbation of asthma.
| Condition |
|---|
|
ASTHMA |
| Study Type: | Observational |
| Official Title: | Measurement of Natriuretic Hormone Peptides in Exacerbation of Asthma |
- The measurement of NHPs after treatment of an exacerbation of asthma [ Time Frame: 14 days ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples With DNA
Samples of blood will be secured in the Division of Allergy/Immunology at the University of South Florida, Joy McCann Culverhouse Airways Disease Center. All samples will be appropriately coded to maintain confidentiality. Blood specimens will be held at minus 20 degrees Celsius. GENETICS SAMPLES ARE OPTIONAL
| Enrollment: | 30 |
| Study Start Date: | February 2009 |
| Study Completion Date: | February 2011 |
| Primary Completion Date: | December 2010 (Final data collection date for primary outcome measure) |
Overall Study Design
- Measurement of Natriuretic Hormone Peptides in individuals suffering from exacerbation of asthma.
- Measurement of Natriuretic Hormone Peptides 5-7 days after initiation of treatment of exacerbation of asthma.
- Measurement of Natriuretic Hormone Peptides 10-14 days after initiation of treatment of exacerbation of asthma.
3 comparisons of Natriuretic Hormone Peptides levels will be made:
- Exacerbation compared to 5-7 days after initiation of treatment
- Exacerbation compared to 10-14 days after initiation of treatment
- 5-7 days after initiation of treatment compared to 10-14 days after initiation of treatment.
Samples of blood will be secured in the Division of Allergy/Immunology at the University of South Florida, Joy McCann Culverhouse Airways Disease Center. All samples will be appropriately coded to maintain confidentiality. Blood specimens will be held at minus 20 degrees Celsius.
Eligibility| Ages Eligible for Study: | 18 Years to 85 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
The Asthma Control Test score of less than 18.
Asthma control test consists of five questions, scored 1-5 each.
Inclusion Criteria:
- Both genders, age 18-85.
- Females who are pregnant or lactating are not eligible.
- Read and comprehend English.
- Ability to give informed consent.
- Seen in the outpatient setting at one of the clinic.
- The subject must have a history of physician diagnosed asthma for at least 1 year and must have an exacerbation of asthma for entry into the study.
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Richard Lockey, prinicpal investigator, University of South Florida |
| ClinicalTrials.gov Identifier: | NCT01690793 History of Changes |
| Other Study ID Numbers: | acute asthma |
| Study First Received: | August 5, 2010 |
| Last Updated: | September 18, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of South Florida:
|
ASTHMA ACUTE EXACERBATION OF ASTHMA |
Additional relevant MeSH terms:
|
Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity |
Immune System Diseases Hormones Natriuretic Agents Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Pharmacologic Actions Cardiovascular Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on June 13, 2013