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Study identifier: NCT06682936 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Feasibility of Ambulatory Talc. Pleurodesis

Condition: Malignant Pleural Effusion · Malignancy · Palliative Care  ·  Sponsor: David Rollins

PhaseNA
Planned participants15
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Patients with malignant pleural disease often experience a significant symptom burden and a short life expectancy. The cornerstone of their treatment is relieving breathlessness by draining fluid from around the lungs and attempting to prevent further fluid build up. Inpatient chest drainage and talc pleurodesis remains the most successful method of stopping the fluid build up but this often requires an average hospital stay of four days. This can be an inappropriate length of time for this patient group. Our study would investigate whether this treatment could be provided on an outpatient, ambulatory basis and facilitate a greater quality of life. The investigators would assess deliverability of the trial protocol and collect patient feedback to see if our patients consider it an acceptable and worthwhile intervention.

This description comes directly from the study's public registry record.

Talk to the study team

Kevin Conroy, MBBS, FRCP  ·  01642624615  ·  kevin.conroy@nhs.net

Always discuss trial participation with your own doctor first.

Locations (1)

North Tees and Hartlepool NHS foundation trustStockton-on-Tees, County Durham, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06682936