Thoracentesis to Alleviate Cardiac Pleural Effusion (TAP-IT)
Primary Purpose
Heart Failure, Pleural Effusion
Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Thoracentesis
Standard-of-care medical treatment
Sponsored by
About this trial
This is an interventional treatment trial for Heart Failure focused on measuring Heart failure, Systolic heart failure, Pleural effusion, Thoracentesis, Thoracocentesis, Pleurocentesis
Eligibility Criteria
Inclusion Criteria:
- Left ventricular ejection fraction (LVEF) ≤ 45%
- Non- negligible pleural effusion by x-ray, ultrasound, CT or MRI, suspected to be due to heart failure
- Age ≥ 18 years
Exclusion Criteria:
- Clinically indicated diagnostic thoracentesis (e.g. suspected malignant aetiology)
- Suspected pulmonary or pleural infection (pneumonia symptoms with c- reactive protein>100 mg/L or white blood count>11)
- Recent (<3 months) intrathoracic procedure (including heart or lung surgery, transcatheter aortic valve implantation (TAVI) or thoracentesis)
- Contraindications to thoracentesis according to local guidelines (such as spontaneously elevated international normalized ratio (INR) or thrombocytopenia), patients on oral anticoagulation may be randomized.
- Severe aortic stenosis
- Massive pleural effusion (equivalent to >2/3 of lung on a standing chest x-ray)
- Substantially affected hemodynamics (systolic blood pressure < 85mmHg, need of inotropes) or high oxygen demand (>7L/min)
- Estimated glomerular filtration rate (eGFR) <15ml/min/1.73m2 or dialysis treatment
- Planned or expected admission > 10 days for other condition than heart failure
- Inability to give informed consent
Sites / Locations
- University Hospital AalborgRecruiting
- University Hospital AarhusRecruiting
- University Hospital Bispebjerg and FrederiksbergRecruiting
- University Hospital RigshospitaletRecruiting
- University Hospital Rigshospitalet, GlostrupRecruiting
- University Hospital Herlev/GentofteRecruiting
- University Hospital NordsjaellandRecruiting
- University Hospital HvidovreRecruiting
- University Hospital OdenseRecruiting
- University Hospital Zealand, RoskildeRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Control group
Intervention group
Arm Description
Standard-of-care medical treatment.
Thoracentesis in addition to standard-of-care medical treatment.
Outcomes
Primary Outcome Measures
Days alive outside of hospital (days)
Number of days the patient is alive outside of hospital in the 90 days following randomization
Secondary Outcome Measures
Satisfaction with hospital stay (Likert scale)
Selected questions from the questionnaire "Questions about your admission" from the annual Danish National Survey of Patient Experiences to assess satisfaction with index admission. Likert scale from 1-5. 5 represents the best outcome.
Kansas City Cardiomyopathy Questionnaire (KCCQ-12) (score)
Kansas City Cardiomyopathy Questionnaire (KCCQ). Selected scores from the 12-item questionnaire, including changes in scores between 14 and 90 days. Scores from 1-100 with 100 representing the best outcome.
Complications during hospital stay (count)
Number of complications during the index admission (eg. infections, delirium, falls, thrombosis)
Complications to thoracentesis (count)
Number of complications to interventional thoracentesis
Duration of index admission (days)
Duration of index admission following randomization.
Changes from baseline in weight during admission (kg)
Changes in weight during admission
Change from baseline in dosage of diuretics during admission (mg/day)
Change in dosage of diuretics during index admission
Time to death (days)
Time to first readmission or death (days)
Full Information
NCT ID
NCT05017753
First Posted
August 12, 2021
Last Updated
August 10, 2022
Sponsor
Bispebjerg Hospital
Collaborators
Independent Research Fund Denmark, Hartmann Fonden, University Hospital Bispebjerg and Frederiksberg
1. Study Identification
Unique Protocol Identification Number
NCT05017753
Brief Title
Thoracentesis to Alleviate Cardiac Pleural Effusion
Acronym
TAP-IT
Official Title
Thoracentesis to Alleviate Cardiac Pleural Effusion - an Interventional Trial (TAP-IT)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 31, 2021 (Actual)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
August 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bispebjerg Hospital
Collaborators
Independent Research Fund Denmark, Hartmann Fonden, University Hospital Bispebjerg and Frederiksberg
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The present study will examine the comparative effectiveness of two treatment strategies currently used in the treatment of patients with systolic heart failure presenting with pleural effusion. Patients will be randomized to standard medical treatment only or medical treatment and referral to thoracentesis.
Study hypothesis: A strategy of referring patients with heart failure-related pleural effusion to thoracentesis increases number of days alive outside of hospital over the following 90 days.
Detailed Description
Purpose and Rationale: Pleural effusion is a common presentation in patients with heart failure, and the condition is related to a poor prognosis and increased mortality. Therapeutic options consist of intensification of diuretic treatment and invasive drainage of the effusion (thoracentesis). Thoracentesis is a common medical procedure and is often performed on patients with heart failure presenting with a pleural effusion, but there is no randomized evidence to guide the use of thoracentesis in heart failure-related pleural effusion. International guidelines provide no recommendations. Some Danish hospitals use thoracentesis frequently, some rarely. Hence, there is true clinical equipoise and a strong need to assess whether thoracentesis benefits patients or not.
Study Hypothesis: A strategy of referring patients with heart failure-related pleural effusion to thoracentesis increases number of days alive outside of hospital over the following 90 days.
Study Setting:126 adult patients admitted with systolic heart failure and pleural effusion documented by either chest x- ray, ultrasound, computed tomography (CT) or magnetic resonance imaging (MRI) will be randomized 1:1 to medical treatment only or medical treatment and referral to thoracentesis. Thoracentesis will be performed according to local practice. Randomization will be stratified according to whether patients are treated with oral anticoagulation.
Crossover/rescue thoracentesis: For patients in the medical treatment arm whose condition deteriorates to the degree that the participant fulfill any of the study exclusion criteria (eg. increased need of oxygen), thoracentesis may be performed immediately. Some patients randomized to medical treatment only may prove to be too diuretic resistant to achieve an adequate effect of medical treatment alone. The recommended waiting period before performing thoracentesis on a patient in the control group is 5 days from randomization.
Patients may be discharged at the discretion of the treating physician. The follow up period is planned to 90 days.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Pleural Effusion
Keywords
Heart failure, Systolic heart failure, Pleural effusion, Thoracentesis, Thoracocentesis, Pleurocentesis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The trial is a pragmatic controlled, randomized, multicenter open label trial with including patients admitted with pleural effusion related to systolic heart failure. Patients will be randomized 1:1 to standard-of-care medical treatment only or standard-of-care medical treatment and referral to thoracentesis. Randomization will be stratified according to whether patients are treated with oral anticoagulation.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
126 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Standard-of-care medical treatment.
Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Thoracentesis in addition to standard-of-care medical treatment.
Intervention Type
Procedure
Intervention Name(s)
Thoracentesis
Other Intervention Name(s)
Thoracocentesis, Pleurocentesis
Intervention Description
Thoracentesis will be performed according to local practice, either at the ward or at the radiology department, in addition to standard-of-care medical treatment.
Intervention Type
Drug
Intervention Name(s)
Standard-of-care medical treatment
Intervention Description
Standard-of-care medical treatment
Primary Outcome Measure Information:
Title
Days alive outside of hospital (days)
Description
Number of days the patient is alive outside of hospital in the 90 days following randomization
Time Frame
90 days
Secondary Outcome Measure Information:
Title
Satisfaction with hospital stay (Likert scale)
Description
Selected questions from the questionnaire "Questions about your admission" from the annual Danish National Survey of Patient Experiences to assess satisfaction with index admission. Likert scale from 1-5. 5 represents the best outcome.
Time Frame
Up til 1 week after discharge
Title
Kansas City Cardiomyopathy Questionnaire (KCCQ-12) (score)
Description
Kansas City Cardiomyopathy Questionnaire (KCCQ). Selected scores from the 12-item questionnaire, including changes in scores between 14 and 90 days. Scores from 1-100 with 100 representing the best outcome.
Time Frame
At 14 days and 90 days - up til 1 week
Title
Complications during hospital stay (count)
Description
Number of complications during the index admission (eg. infections, delirium, falls, thrombosis)
Time Frame
From randomization until the date af discharge from hospital. Estimated time frame from 2 days to 3 weeks.
Title
Complications to thoracentesis (count)
Description
Number of complications to interventional thoracentesis
Time Frame
From randomization until the date af discharge from hospital. Estimated time frame from 2 days to 3 weeks.
Title
Duration of index admission (days)
Description
Duration of index admission following randomization.
Time Frame
From randomization until the date af discharge from hospital. Estimated time frame from 2 days to 3 weeks.
Title
Changes from baseline in weight during admission (kg)
Description
Changes in weight during admission
Time Frame
From randomization until the date af discharge from hospital. Estimated time frame from 2 days to 3 weeks.
Title
Change from baseline in dosage of diuretics during admission (mg/day)
Description
Change in dosage of diuretics during index admission
Time Frame
From randomization until the date af discharge from hospital. Estimated time frame from 2 days to 3 weeks.
Title
Time to death (days)
Time Frame
90 days
Title
Time to first readmission or death (days)
Time Frame
90 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Left ventricular ejection fraction (LVEF) ≤ 45%
Non- negligible pleural effusion by x-ray, ultrasound, CT or MRI, suspected to be due to heart failure
Age ≥ 18 years
Exclusion Criteria:
Clinically indicated diagnostic thoracentesis (e.g. suspected malignant aetiology)
Suspected pulmonary or pleural infection (pneumonia symptoms with c- reactive protein>100 mg/L or white blood count>11)
Recent (<3 months) intrathoracic procedure (including heart or lung surgery, transcatheter aortic valve implantation (TAVI) or thoracentesis)
Contraindications to thoracentesis according to local guidelines (such as spontaneously elevated international normalized ratio (INR) or thrombocytopenia), patients on oral anticoagulation may be randomized.
Severe aortic stenosis
Massive pleural effusion (equivalent to >2/3 of lung on a standing chest x-ray)
Substantially affected hemodynamics (systolic blood pressure < 85mmHg, need of inotropes) or high oxygen demand (>7L/min)
Estimated glomerular filtration rate (eGFR) <15ml/min/1.73m2 or dialysis treatment
Planned or expected admission > 10 days for other condition than heart failure
Inability to give informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Signe Glargaard, MD
Phone
61696721
Ext
+45
Email
signe.glargaard@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Jens Jakob Thune, MD, Ph.D.
Phone
24428389
Ext
+45
Email
jens.jakob.thune@regionh.dk
Facility Information:
Facility Name
University Hospital Aalborg
City
Aalborg
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Aarhus
City
Aarhus
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Bispebjerg and Frederiksberg
City
Copenhagen
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Rigshospitalet
City
Copenhagen
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Rigshospitalet, Glostrup
City
Glostrup
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Herlev/Gentofte
City
Herlev
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Nordsjaelland
City
Hillerød
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Hvidovre
City
Hvidovre
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Odense
City
Odense
Country
Denmark
Individual Site Status
Recruiting
Facility Name
University Hospital Zealand, Roskilde
City
Roskilde
Country
Denmark
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Thoracentesis to Alleviate Cardiac Pleural Effusion
We'll reach out to this number within 24 hrs