Talc Pleurodesis for Malignant Pleural Effusion on Outpatient Basis
ambulatory chest drain and talc pleurodesis
Neoplasms+6
+ Neoplasms by Site
+ Pleural Diseases
Other Study
Summary
Study start date: January 10, 2024
Actual date on which the first participant was enrolled.This clinical trial investigates whether a procedure known as talc pleurodesis can be effectively performed on an outpatient basis for patients with malignant pleural effusion, which is a condition where fluid builds up around the lungs due to cancer. By performing the procedure outside of the hospital, the study aims to make treatment more convenient for patients and potentially reduce hospital stays and associated costs. The trial targets patients who are eligible for this procedure and offers them a chance to participate in the study in addition to receiving standard care options. During the study, participants undergo a process starting on the first day where a chest drain is inserted to remove fluid from the chest cavity. The fluid is drained in stages throughout the day, and patients go home with a special bag to collect any remaining fluid. On the second day, if the fluid removal is successful and the lung is fully expanded, talc is introduced into the chest to prevent fluid from accumulating again, and the process of draining and monitoring continues. By the third day, if the fluid accumulation has resolved, the drain is removed, and the success of the procedure is confirmed with a chest x-ray. Participants are also asked to fill out short questionnaires regarding their breathing, pain levels, and overall satisfaction with the procedure, which helps measure the trial's success.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.15 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
North Tees and Hartlepool NHS foundation trust
Stockton-on-Tees, United KingdomOpen North Tees and Hartlepool NHS foundation trust in Google Maps