Outcomes in Patients and Their Closest Relatives Treated for Congenital Heart Disease With Catheter Based or Surgical Techniques (MEQC)
Primary Purpose
Congenital Heart Defects
Status
Unknown status
Phase
Early Phase 1
Locations
Norway
Study Type
Interventional
Intervention
Percutaneous pulmonary valve implantation or open heart surgery
Sponsored by
About this trial
This is an interventional health services research trial for Congenital Heart Defects focused on measuring quality of life, congenital heart disease, open heart surgery, percutaneous pulmonary valve implantation, costs
Eligibility Criteria
Inclusion Criteria:
- secure indication of pulmonary valve dysfunction (stenosis and, or regurgitation)
- an indication of surgical correction
- body weight according to the recommendation from the producer of the device
- moderate to serious dilatation of right ventricle
- considerable leak in the tricuspidal valve
- information from former surgery; conduit size, gradient of the stenosis measured by EKKO/MR/ catheterization, X-ray.
- be able to speak and communicate well in Norwegian.
Exclusion Criteria:
- aggressive endocarditis
- not circumferential deposit of calcium
- < 20 kg
- not able to understand, speak or communicate well in Norwegian
Sites / Locations
- The Interventional Centre, Rikshospitalet, Oslo University HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
quality of life, clinical outcomes and costs
Arm Description
Quality of life, clinical outcomes and costs after two different treatment options in patients and closest relatives
Outcomes
Primary Outcome Measures
Quality of life
Percutaneous pulmonary valve implantation or open heart surgery; what are the patients and their closest relatives narrative experiences. Measured before the event, 1, 3, 6, and 12 month's after treatment.
Secondary Outcome Measures
Clinical outcomes
What is the relationship between patient reported outcomes and clinical outcomes before, 1, 3, 6 and 12 months after the treatment
Is there a difference in the effect of percutaneous versus open surgical technique on operative time, complication rate and reoperations in the peri- and postoperative period?
Are there savings in costs related to the individual and their family and society between the two techniques?
In order to describe and compare the differences in costs with patients outcomes and quality-adjusted life years, this study aim to calculate both in-hospital care and out-patient clinical costs between percutaneous pulmonary valve implantation and conventional open heart surgery. Measured Before the event, 1, 3, 6 and 12 months after surgery.
Full Information
NCT ID
NCT01421030
First Posted
June 24, 2011
Last Updated
September 24, 2012
Sponsor
Oslo University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01421030
Brief Title
Outcomes in Patients and Their Closest Relatives Treated for Congenital Heart Disease With Catheter Based or Surgical Techniques
Acronym
MEQC
Official Title
Outcomes in Patients and Their Closest Relatives Treated for Congenital Heart Disease With Catheter Based or Surgical Techniques.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2012
Overall Recruitment Status
Unknown status
Study Start Date
September 2011 (undefined)
Primary Completion Date
September 2012 (Anticipated)
Study Completion Date
September 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study compares clinical, self- reported and cost outcomes in children and adolescents treated with pulmonary valve implantation, percutaneous versus open surgical technique. Since cardiac surgery in children and adolescents affect the whole family, the experience of the patients and their closest relatives are recorded and analysed separately. Cost may be an important factor in the choice of technology (1). Hence, the present study also aims to compare savings in costs, percutaneous versus open technique, related to the individual, their family and society.
1.2 Research questions
Percutaneous pulmonary valve implantation or open heart surgery; what are the patients' and their closest relatives narrative experiences
Is there a difference in patient and their closest relatives reported outcomes, measured as health related quality of life, in patients with congenital pulmonary disease before the event, 1, 3, 6 and 12 months after percutaneous intervention versus open heart surgery approach?
What is the relationship between patient reported outcomes and clinical outcomes before, 1, 3, 6 and 12 months after the treatment?
Are there savings in costs related to the individual and their family and society between the two techniques?
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Defects
Keywords
quality of life, congenital heart disease, open heart surgery, percutaneous pulmonary valve implantation, costs
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
quality of life, clinical outcomes and costs
Arm Type
Other
Arm Description
Quality of life, clinical outcomes and costs after two different treatment options in patients and closest relatives
Intervention Type
Procedure
Intervention Name(s)
Percutaneous pulmonary valve implantation or open heart surgery
Intervention Description
Outcomes before percutaneous pulmonary valve implantation or open heart surgery before, 1, 3, 6 and 12 months after the treatment
Primary Outcome Measure Information:
Title
Quality of life
Description
Percutaneous pulmonary valve implantation or open heart surgery; what are the patients and their closest relatives narrative experiences. Measured before the event, 1, 3, 6, and 12 month's after treatment.
Time Frame
up to 12 month's after treatment
Secondary Outcome Measure Information:
Title
Clinical outcomes
Description
What is the relationship between patient reported outcomes and clinical outcomes before, 1, 3, 6 and 12 months after the treatment
Is there a difference in the effect of percutaneous versus open surgical technique on operative time, complication rate and reoperations in the peri- and postoperative period?
Time Frame
up to 12 months after treatment
Title
Are there savings in costs related to the individual and their family and society between the two techniques?
Description
In order to describe and compare the differences in costs with patients outcomes and quality-adjusted life years, this study aim to calculate both in-hospital care and out-patient clinical costs between percutaneous pulmonary valve implantation and conventional open heart surgery. Measured Before the event, 1, 3, 6 and 12 months after surgery.
Time Frame
up to 12 months after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
secure indication of pulmonary valve dysfunction (stenosis and, or regurgitation)
an indication of surgical correction
body weight according to the recommendation from the producer of the device
moderate to serious dilatation of right ventricle
considerable leak in the tricuspidal valve
information from former surgery; conduit size, gradient of the stenosis measured by EKKO/MR/ catheterization, X-ray.
be able to speak and communicate well in Norwegian.
Exclusion Criteria:
aggressive endocarditis
not circumferential deposit of calcium
< 20 kg
not able to understand, speak or communicate well in Norwegian
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Brith Andresen, Can san
Phone
+4723070162
Email
brith.andresen@oslo-universitetssykehus.no
First Name & Middle Initial & Last Name or Official Title & Degree
Erik Fosse, Professor/Head of Department
Phone
+4723070116
Email
erik.fosse@oslo-universitetssykehus.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erik Fosse, Professor/Head of Department
Organizational Affiliation
The Interventional Centre, Rikshospitalet, Oslo University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Interventional Centre, Rikshospitalet, Oslo University Hospital
City
Oslo
State/Province
Sognsvannsvn 20
ZIP/Postal Code
0027
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Erik Fosse, Professor/Head of Department
Phone
+4723070116
Email
erik.fosse@oslo-universitetssykehus.no
First Name & Middle Initial & Last Name & Degree
Erik Fosse, Professor
12. IPD Sharing Statement
Learn more about this trial
Outcomes in Patients and Their Closest Relatives Treated for Congenital Heart Disease With Catheter Based or Surgical Techniques
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