Skip to content

Clinical Study of Relationship Between Granulocyte Activation, HDAC2 and Severe Asthma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02881502
Enrollment
60
Registered
2016-08-29
Start date
2016-06-30
Completion date
2017-07-31
Last updated
2016-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

granulocyte activation, HDAC2, severe asthma

Brief summary

Program: Clinical Study of Relationship Between Granulocyte Activation, HDAC2 and Severe Asthma Aim:The early prediction of severe asthma, early intervention on the disease, reduce the family and the national finance. design:This study is a single center randomized controlled trial designed by the Department of respiratory medicine, Xijing Hospital, as the main research unit.Compare the case group(severe asthma group and mild-and-moderate asthma group) and control group(healthy control group) by detecting the activity of MPO、NE、MMP-9 and ECP in the peripheral blood and the activity of HDAC2 in PBMCs of patients. case:60 Case selection: Inclusion criteria: age 18-75 years old; diagnosis of asthma was clear; informed consent was signed. Exclusion criteria: poor compliance; cognitive ability is low; psychiatric disorders need to be combined with psychotropic medication.

Detailed description

Application of SPSS 19 statistical software. Measurement data were expressed as mean ± standard deviation. First the data is normality tested and homogeneity of variance tested, according to the measurement data of normal distribution by SNK single factor analysis of variance; does not conform to the normal distribution of measurement data, using the Kruskal Wallis non parametric test. P \< 0.05 for the difference was statistically significant.

Interventions

OTHERsevere asthma group

No intervention

Sponsors

Xijing Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

healthy control group: * Mainly from students, * family members of patients without chronic lung disease, * healthy population, * age 18-75 years old, the gender is not limited. case group: * The patient has been diagnosed with asthma in the outpatient clinic. The diagnostic criteria are in accordance with the Guidelines for Prevention and Treatment of Bronchial Asthma in the respiratory disease branch of the Chinese Medical Association. In the past 1 year need guidelines of global asthma record instrument 4-5 drug treatment of asthma \[high dose inhaled corticosteroid with long-acting beta2 receptor agonist or leukotriene modifiers / theophylline or systemic hormone therapy is more than or equal to 50% of the time, in order to prevent into uncontrolled asthma, or even in the treatment is to control asthma patients for severe asthma.

Exclusion criteria

: * Poor treatment compliance, or low cognitive ability to impact the self rating scale ; * There are serious heart, liver, renal dysfunction, or other infectious diseases ; * The individual who refuse to sign the informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Evidence of clinically definite severe asthma confirmed by the plasma concentration of blood related indexes(MPO、MMP-9、NE、ECP、HDAC2)one yearCompare the difference was not statistically significant of the different groups by testing the concentration of blood related indicators of subjects

Countries

China

Contacts

Primary ContactGuo H qin, Graduate
hqgsunshine@163.com18194278935

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026