Lysophosphatidylglycerol in Asthma Pathogenesis
1 other identifier
observational
250
1 country
1
Brief Summary
The study aims to investigate the relationship between the small molecule metabolite lysophosphatidylglycerol and asthma clinical features and explore its involvement in asthma pathogenesis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2015
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2015
CompletedFirst Submitted
Initial submission to the registry
March 17, 2024
CompletedFirst Posted
Study publicly available on registry
March 25, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedMarch 26, 2024
March 1, 2024
10 years
March 17, 2024
March 24, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
lipidomics
collect blood for lipidomic analysis and in vitro assays on Day1
when enrolled
Eligibility Criteria
Patients with asthma who visited or were hospitalized in the Department of Respiratory and Critical Care Medicine of Peking University Third Hospital, who met the asthma diagnostic criteria proposed in the Bronchial Asthma Prevention and Treatment Guidelines and healthy controls without history or symptoms of chronic respiratory disease, allergic status or other conditions that could affect the outcome.
You may qualify if:
- \. clinical diagnosis of asthma.
You may not qualify if:
- Combined with chronic obstructive pulmonary disease, bronchiectasis, pneumonia, obstructive sleep apnea hypopnea syndrome, malignant tumor
- Combined with acute and chronic respiratory failure
- Combined with severe cardiovascular disease
- Pregnant woman.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peking university third hospital
Beijing, None Selected, 100191, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chun Chang
Peking University Third Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 17, 2024
First Posted
March 25, 2024
Study Start
January 1, 2015
Primary Completion
December 31, 2024
Study Completion
June 30, 2025
Last Updated
March 26, 2024
Record last verified: 2024-03