Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date May 2022
Source Naestved Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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.

Study Design


Intervention

Diagnostic Test:
Systematic lung ultrasound
Patients will undergo a systematic lung ultrasound including review of: Sonographic characteristic of effusion Parietal, diaphragmatic and visceral pleura Pleural nodules Lung parenchyma Extra pulmonary findings: Hepatic pathology, enlarged lymph nodes of the neck and a cardiac assessment.

Locations

Country Name City State
Denmark Næstved Sygehus, department of pulmonary medicine Næstved Region Sjælland

Sponsors (1)

Lead Sponsor Collaborator
Naestved Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

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
See also
  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