- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06275178
Medical Thoracoscopy for Diagnosing Unexplained Pleural Effusion: a National Multicenter Retrospective Study
February 17, 2024 updated by: Gang Hou, China-Japan Friendship Hospital
This study is a national multicenter retrospective study.
Patients with unexplained pleural effusion who underwent thoracoscopic or video-assisted thoracoscopic biopsy for patients in recent 10 years were retrospectively collected from multiple centers to understand the proportion and final etiological composition of pleural effusion in China.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
5000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Gang Hou, MD
- Phone Number: 010-84205729
- Email: hougangcmu@163.com
Study Contact Backup
- Name: Mingming Deng, PhD
- Phone Number: +86 18801336854
- Email: isdeng@163.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with pleural effusion who underwent medical thoracoscopy were included in the study.
Patients who could not obtain a final diagnosis were excluded from the study
Description
Inclusion Criteria:
Patients with unexplained pleural effusion who underwent thoracoscopic or video-assisted thoracoscopic biopsy
Exclusion Criteria:
Patients who cannot obtain a final diagnosis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The proportion of fibrinous pleurisy in Chinese population
Time Frame: December 31, 2024
|
The proportion of fibrinous pleurisy in Chinese population
|
December 31, 2024
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 20, 2024
Primary Completion (Estimated)
December 24, 2024
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
February 17, 2024
First Submitted That Met QC Criteria
February 17, 2024
First Posted (Actual)
February 23, 2024
Study Record Updates
Last Update Posted (Actual)
February 23, 2024
Last Update Submitted That Met QC Criteria
February 17, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ZRJY2021-BJ08-02-04
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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