Clinical Trials Directory

Trials / Completed

CompletedNCT00188474

A Quality of Life Study re Management of Malignant Pleural Effusions

A Prospective Study of Patient Centered Outcomes in the Management of Malignant Pleural Effusions

Status
Completed
Phase
Study type
Observational
Enrollment
149 (actual)
Sponsor
University Health Network, Toronto · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

There is much data in the literature regarding optimal treatment approaches for malignant pleural effusions as assessed by patient outcomes. However, data on quality of life and satisfaction with treatment from the patient's perspective is not available.

Detailed description

This study will compare various treatment strategies in the management of malignant pleural effusions with respect to: 1. Primary endpoint: the successful palliation of symptomatic pleural effusions as assessed by the London Chest Activity of Daily Living Scale (LCADLS) 2. Secondary endpoints: i) impact of treatment on patient quality of life as assessed by the Functional Assessment of Chronic Illness Therapy - Palliative patient (FACIT-PAL) questionnaire ii) Assessment of patient satisfaction with treatment received via Functional Assessment of Chronic Illness Therapy-Treatment Satisfaction (FACIT-TS) questionnaire iii)Pleurodesis success rates assessed by 2 and 6-week effusion control rates on CXR iv) Requirement of further hospitalizations or procedures for the treatment of recurrent effusions v) Comparison of morbidity and mortality rates for differing treatment approaches vi) comparison of cost in a Canadian health care setting for differing treatment approaches

Conditions

Interventions

TypeNameDescription
BEHAVIORALLCADLS, FACIT-PAL, FACIT-TS questionnairesLCADLS, FACIT-PAL, FACIT-TS questionnaires

Timeline

Start date
2004-08-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2005-09-16
Last updated
2017-05-04

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00188474. Inclusion in this directory is not an endorsement.