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Clinical Trials in China / NCT07208409
Starting soon Not applicable

Pleurodesis in Small-bore Chest Tube

NCT07208409 · tracked via the Priya Life Science China tracker
Sponsor
The University of Hong Kong
Phase
Not applicable
Started
2026-02-01
Last updated
2025-12-24

Condition(s) studied

Pleural Effusion, Malignant

Investigational drug(s) / intervention(s)

14 Fr chest tube12 Fr chest tube8 Fr chest tube

14 Fr chest tube: Chest tube size of 14Fr will be inserted

12 Fr chest tube: Chest tube of 12 Fr will be inserted

8 Fr chest tube: Chest tube size of 8Fr will be inserted

Study summary

Malignant pleural effusion (MPE) imposes a high burden on the healthcare system in the Asian Pacific region, as lung and breast cancer are the commonest cancers associated with malignant pleural effusion, as the two commonest cancers in the Asian Pacific region.

While indwelling pleural catheter (IPC), a catheter that is inserted for long-term drainage of pleural fluid, is not commonly used in Asian countries, small-bore chest tubes are increasingly used due to their ease of insertion and causing less pain.

Injecting talc, a chemocal, to promote adhesion of pleura, called talc pleurodesis was an effective method of managing MPE. However, the optimal size of small-bore chest tubes and the feasibility of talc pleurodesis have not been thoroughly investigated.

This randomised controlled trial aims to evaluate the feasibility and success rate of pleurodesis using small-bore chest drains and to examine the outcomes associated with different sizes of these drains, namely 8 Fr, 12 Fr, and 14 Fr, in managing MPE.

The primary outcome is the feasibility of talc pleurodesis with different small-bore chest tubes. Secondary outcomes include the differences in recurrence rates post-pleurodesis between small-bore and ultra-small-bore chest tubes, as well as patient outcomes such as pain scores, SpO2/FiO2 ratios (oxygen saturation/fractional inspired oxygen ratio), and complications.

The sample size will be 60, and the project will be carried out over one year.

The outcome of this study can serve as a reference for managing MPE regarding the feasibility, safety, and efficacy of ultra-small-bore chest tubes worldwide, particularly in the Asia-Pacific region, where IPC is less common.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Pleural effusion. * With clinical indications for pleural drainage and chest drain insertion. * With anticipated need for pleurodesis e.g. known malignancy, no clinical signs of pleural infection. * age ≥18 year-old Exclusion Criteria: * Pleural effusion not sizable for drainage. * With clinical suspicion of pleural infection e.g. pleuritic chest pain, fever, ultrasound showed loculated pleural effusion * Age ≤18 year-old

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The University of Hong Kong, Queen Mary Hospital Hong Kong China

More The University of Hong Kong trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07208409 on ClinicalTrials.gov ↗ ← All trials in China