CClinicalTrials.gg
Status unknownNCT02881502Updated Aug 29, 2016

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

An observational study in Asthma, sponsored by Xijing Hospital. Status unknown at 1 site in China. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-08-29.

Sponsored by Xijing Hospital · Observational

The sponsor has not verified this record recently (last verified Aug 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
60
Ages
18 Years to 75 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Asthma

Browse trials for

Keywords

  • granulocyte activation
  • HDAC2
  • severe asthma
03

In context

Asthma

3,921 studies on the registry are indexed under Asthma; 506 are open to participants now.

This study's planned enrollment of 60 is below the median of 150 across 970 observational studies indexed under Asthma.

Browse Asthma studies →

Lead sponsor

Xijing Hospital is the lead sponsor of 465 studies on the registry; 157 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

outpatients and the students

Eligibility criteria

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.
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
60 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • 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.

  • mild and moderate asthma group

    Patients diagnosed with asthma in the outpatient clinic, in accordance with the inclusion criteria and exclusion criteria.

  • severe asthma group

    Outpatient patients with severe asthma diagnosis, in accordance with the inclusion criteria and exclusion criteria.

    Other: severe asthma group

Interventions

  • Othersevere asthma group

    No intervention

06

What researchers measure

Primary outcomes

  1. Evidence of clinically definite severe asthma confirmed by the plasma concentration of blood related indexes(MPO、MMP-9、NE、ECP、HDAC2)

    Compare the difference was not statistically significant of the different groups by testing the concentration of blood related indicators of subjects

    Time frame: one year

07

Study locations

1 of 1 sites recruiting
  • XijingH
    Xian, Shanxi 780032, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 29, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02881502
Lead sponsor
Xijing Hospital
Responsible party
Haiqin Guo (Master Degree Candidate,Student of Respiratory Medicine, Xijing Hospital) — Principal investigator
First posted
Aug 29, 2016
Start date
Jun 2016
Primary completion
Jul 2017 (estimated)
Completion
Jul 2017 (estimated)
Last update
Aug 29, 2016

Study contacts

Guo H qin, Graduate
Contact
hqgsunshine@163.com
18194278935 ext. 029
Wu C gui, professor
study director · Xijing Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion