Patients share their stories about living with fluid in the lungs
NCT ID NCT03235999
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study interviewed 10 adults with malignant pleural effusion (fluid buildup around the lungs due to cancer) to learn about their experiences with the condition and its treatments. Participants had either talc pleurodesis or an indwelling pleural catheter. The goal was to gather insights through in-depth interviews, not to test a new treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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10 people
The number who actually took part.
- Started
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Jun 2016
- Finished
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Jan 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with malignant pleural effusions
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adults diagnosed with a malignant pleural effusion 2. Has undergone either talc pleurodesis or IPC 3. Have signed a consent form prior to entering the study 4. Life expectancy \> 6 weeks based on LENT guidelines (Low/Moderate risk group) - The LENT score calculation assigns 0 (\<1500 IU/L) or 1 (\>1500 IU/L) for pleural fluid LDH level; 0 to 3 points for matching ECOG performance scores (3 and 4 are combined); 0 (\<9) or 1 (\>9) for neutrophil-to-lymphocyte ratio; and 0 (lowest risk), 1 (moderate risk), or 3 (highest risk) for tumor type. Exclusion Criteria: 1. Any patient who is unable to understand sufficient English to take part in the semi-structured interviews 2. Weakness or fatigue sufficient so that the patient is unable to take part in the interviews
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Gloucestershire Hospitals NHS Foundation Trust
Cheltenham, Gloucestershire, GL53 7AN, United Kingdom
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Other studies related to the condition(s) this trial covers.
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