Pleural Effusion Clinical Trial
Official title:
Value of Additional Upfront Systematic Lung Ultrasound in the Workup of Patients With Unilateral Pleural Effusion: A Prospective Cohort Study
NCT number | NCT04235998 |
Other study ID # | SJ-789 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | February 17, 2020 |
Est. completion date | May 6, 2021 |
Verified date | May 2022 |
Source | Naestved Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The value of lung ultrasound in the work up of pleural effusion (fluid in between the thin doublet layered film surrounding the lungs) is unknown. The researchers will perform a systematic lung ultrasound scan including a scan for extra thoracic metastasis (spread of cancer to other organs) in the lymphnodes of the neck and metastasis lever in 56 patients one-sided pleural effusion. The researchers will measure if the interventions change the diagnostic plan for the patient and leads to faster diagnostics of the underlying course.
Status | Completed |
Enrollment | 57 |
Est. completion date | May 6, 2021 |
Est. primary completion date | November 20, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age = 18 years. - Unilateral pleural effusion of unknown course. - Patients must be able to give informed consent. Exclusion Criteria: - Bilateral pleural effusions. - Known cause of pleural effusions. - Life expectancy <3 months. - Inability to understand written or spoken Danish. |
Country | Name | City | State |
---|---|---|---|
Denmark | Næstved Sygehus, department of pulmonary medicine | Næstved | Region Sjælland |
Lead Sponsor | Collaborator |
---|---|
Naestved Hospital |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of cases where systematic lung ultrasound (LUS) change the planned diagnostic process for patients with unilateral pleural effusion. | Information found in electronic patient files. Comparison of diagnostics planned before systematic ultrasound and diagnostics planned after systematic ultrasound. Measured in proportion of included patients | 26 weeks post procedure | |
Secondary | Characteristics of ultrasonic findings with additional systematic LUS. | Characteristics is recorded in the ultrasound protocol | Day 1, within 30 minutes after the end of procedure | |
Secondary | Proportion of cases where findings of clinical importance on systematic LUS were not identified at the initial contrast-enhanced CT thorax or PET-CT | CT thorax and PET-CT (as assessed by radiologist or clinician at the initial planning of diagnostic work-up) | Day 1 within 30 minutes after the end of procedure | |
Secondary | Proportion of cases where the change in the diagnostic process after LUS provide a diagnose | Information found in electronic patient files. | 26 weeks post procedure | |
Secondary | The patient experienced pain during procedure score | Measured by a VAS (Visual Analogue Scale) scale 0-10, 0 being no pain, 10 being the worse pain | Day 1 within 30 minutes after the end of procedure | |
Secondary | Patient experienced time consumption | Measured by a 3-point Likert scale , scale1-3, 1 being not time consuming at all, 3 being very time consuming | Day 1 within 30 minutes after the end of procedure | |
Secondary | The patients willingness to have the same examination again in the future if necessary | Measured by a 5-point Likert scale, scale 1-5, 1 being definitely willing to have the examination again, 5 being definitely not willing to have the examination again | Day 1within 30 minutes after the end of procedure | |
Secondary | Mean extra time spend on systematic LUS compared to conventional US for guidance of thoracentesis | Measured in minutes. | Day 1 within 30 minutes after the end of procedure |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04159831 -
A Study to Evaluate LTI-01 in Patients With Infected, Non-draining Pleural Effusions
|
Phase 2 | |
Recruiting |
NCT02891642 -
Liquid Biopsy With Immunomagnetic Beads Capture Technique for Malignant Cell Detection in Body Fluid
|
||
Completed |
NCT02232841 -
Electrical Impedance Imaging of Patients on Mechanical Ventilation
|
N/A | |
Completed |
NCT02045641 -
Pleural and Pericardial Effusion Following Open Heart Surgery
|
N/A | |
Completed |
NCT01948076 -
Evaluation of a Pocket-Sized Ultrasound Device As an Aid to the Physical Examination
|
N/A | |
Completed |
NCT01416519 -
Physiotherapy Technique Decreases Respiratory Complications After Cardiac Operation
|
N/A | |
Completed |
NCT01560078 -
Efficacy Study of Thrice Weekly Directly Observed Treatment Short-Course Regimen in Tubercular Pleural Effusion
|
N/A | |
Completed |
NCT04891705 -
Point of Care Ultrasound Lung Artificial Intelligence (AI) Validation Data Collection Study
|
||
Recruiting |
NCT05759117 -
Prospective Evaluation of Patients With Pleural Effusion
|
||
Recruiting |
NCT05910112 -
Prospective Data Collection on Clinical, Radiological and Patient Reported Outcomes After Pleural Intervention
|
||
Completed |
NCT03896672 -
Clinical Implementation of the Use of Positive Pressure in Chest Drainage
|
N/A | |
Active, not recruiting |
NCT06075836 -
AI Assisted Detection of Chest X-Rays
|
||
Recruiting |
NCT03728491 -
Education and Training Competences in Thoracic Ultrasound
|
N/A | |
Not yet recruiting |
NCT03260088 -
Evaluation Of Pleural Effusion At Assiut University Hospital
|
N/A | |
Completed |
NCT03535883 -
The Safety of Thoracentesis, Tunneled Pleural Catheter, and Chest Tubes in Patients Taking Novel Oral Anti-Coagulants
|
||
Completed |
NCT03296280 -
Evaluation of Implementation of a National Point-of-Care Ultrasound Training Program
|
||
Completed |
NCT03661801 -
Novel Pleural Fluid, Biopsy and Serum Biomarkers for the Investigation of Pleural Effusions
|
||
Completed |
NCT01778270 -
Not Invasive Monitoring of Pleural Drainage
|
N/A | |
Terminated |
NCT00402896 -
Malignant Pleural Effusion With ZD6474
|
Phase 2 | |
Recruiting |
NCT00103766 -
Alteplase for Treatment of Empyema and Complicated Parapneumonic Effusion
|
N/A |