Pulmonary Infection After Ischemic Stroke

NCT ID: NCT05923034

Last Updated: 2023-06-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-01

Study Completion Date

2023-07-20

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To assess the frequency of signs of pulmonary infection on a chest CT and development of clinical diagnose of poststroke pneumonia,and its effect on functional outcome in patients with acute ischemic stroke.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Had a Computed Tomography Scan of the Chest Within 24 Hours After Stroke Onset

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

had a computed tomography scan of the chest within 24 hours after stroke onset

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Have a computed tomography scan of the chest within 24 hours after stroke onset

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Capital Medical University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ji Xunming,MD,PhD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Suzhou Municipal Hospital

Suzhou, Anhui, China

Site Status RECRUITING

People Hospital of Rongcheng

Baoding, Hebei, China

Site Status RECRUITING

The Second Hospital of Hebei Medical University

Shijiazhuang, Hebei, China

Site Status RECRUITING

People Hospital of Ningjin

Xingtai, Hebei, China

Site Status RECRUITING

Shihezi Municipal Hospital

Shihezi, Xinjiang, China

Site Status RECRUITING

Xuanwu Hospital, Capital Medical University

Beijing, , China

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

China

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Xunming Ji, MD

Role: CONTACT

010-83199439

Nan Yang, MM

Role: CONTACT

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Zhengfei Ma, MD

Role: primary

Mengge Zhang, MM

Role: primary

Fang Xue, MD

Role: primary

Fei Gu, MD

Role: primary

Naren Ya

Role: primary

Nan Yang, MM

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

PICAS

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Post-stroke Cognitive Impairment
NCT05653141 ACTIVE_NOT_RECRUITING