ClinicalTrials.gg
Not yet recruitingNCT06275178Updated Feb 23, 2024

Medical Thoracoscopy for Diagnosing Unexplained Pleural Effusion: a National Multicenter Retrospective Study

An observational study in Pleural Effusion, Pleural Effusion, Malignant and Fibrinous Pleuritis, sponsored by China-Japan Friendship Hospital. Not yet recruiting. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2024-02-23.

Primary conditionPleural Effusion, MalignantRegistry: Pleural EffusionReclassifiedWhy we changed it
Registry
Pleural Effusion — the first condition term the registry derived for this study.
ClinicalTrials.gg
Pleural Effusion, Malignant
Why
  1. The study's listed conditions name Pleural Effusion, Malignant, a narrower term within Pleural Effusion.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by China-Japan Friendship Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
5,000
Ages
18 Years to 80 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Pleural Effusion
  • Pleural Effusion, Malignant
  • Fibrinous Pleuritis

Browse trials for

03

In context

Pleural Effusion, Malignant Reclassified

169 studies on the registry are indexed under Pleural Effusion, Malignant; 39 are open to participants now.

This study's planned enrollment of 5,000 is above the median of 112 across 37 observational studies indexed under Pleural Effusion, Malignant.

Browse Pleural Effusion, Malignant studies →

Lead sponsor

China-Japan Friendship Hospital is the lead sponsor of 178 studies on the registry; 111 are open to participants now.

Compared within Pleural Effusion, Malignant, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Pleural Effusion. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Patients with unexplained pleural effusion who underwent thoracoscopic or video-assisted thoracoscopic

Exclusion criteria

Exclusion Criteria:

Patients who cannot obtain a final diagnosis

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
5,000 participants (estimated)
Patient registry
No

Interventions

  • ProcedureMedical thoracoscopy

    The included particpants are the patients with unexplained pleural effusion who underwent thoracoscopic or video-assisted thoracoscopic biopsy.

06

What researchers measure

Primary outcomes

  1. The proportion of fibrinous pleurisy in Chinese population

    The proportion of fibrinous pleurisy in Chinese population

    Time frame: December 31, 2024

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Mar 2024; primary completion for Dec 2024, 9 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 17, 2024
First posted
Feb 23, 2024
StartEst.
Mar 20, 2024
Primary completionEst.
Dec 24, 2024
CompletionEst.
Dec 31, 2024
Last update
Feb 23, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 23, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06275178
Responsible party
Gang Hou (Principal Investigator, China-Japan Friendship Hospital) — Principal investigator
First posted
Feb 23, 2024
Start date
Mar 20, 2024 (estimated)
Primary completion
Dec 24, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Feb 23, 2024

Study contacts

Gang Hou, MD
Contact
hougangcmu@163.com
010-84205729
Mingming Deng, PhD
Contact
isdeng@163.com
+86 18801336854

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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