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Catheter-Directed Venous Thrombolysis in Acute Iliofemoral Vein Thrombosis (CaVenT)

Primary Purpose

Deep Vein Thrombosis

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
catheter-directed venous thrombolysis
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Deep Vein Thrombosis focused on measuring Thrombolytic therapy, Postphlebitic syndrome, Venous thrombosis

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Onset of symptoms <21 days Objectively verified DVT of the femoral or common iliac veins or the combined iliofemoral segment Informed consent Exclusion Criteria: Anticoagulant therapy prior to trial entry >7 days Contraindications to thrombolytic therapy Indications for thrombolytic therapy, i.e. phlegmasia coerulea dolens or vena cava thrombosis Severe anemia, hemoglobin (hgb)<8 g/dl Thrombocytopenia, platelets <80x10^9/l Severe renal failure, creatinine clearance <30ml/min Severe hypertension, systolic (syst) blood pressure (BP)>160 mmHg or diastolic (diast) BP >100 mmHg pregnancy Less than 14 days post-surgery or post-trauma History of subarachnoidal or intracerebral bleeding Disease with life expectancy <24 months Drug abuse or mental disease that may interfere with treatment and follow-up Former ipsilateral proximal DVT Chemotherapy or advanced malignant disease

Sites / Locations

  • Ullevaal University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

I

II

Arm Description

Outcomes

Primary Outcome Measures

Patency after 6 months
Post-thrombotic syndrome after 2 years (yrs)

Secondary Outcome Measures

Frequency of clinically relevant bleeding complications
Effects on quality of life
Cost-effectiveness of treatment
Procedural success of CDT
Patency at 2 years
PTS at 6, 12, 36, 48 and 60 months
Relation between PTS and patency
Prevalence of vein anomalies
Prevalence of underlying thrombophilia
Frequency of recurrent venous thrombotic events (VTE)
Markers of importance for recurrent thrombosis
Markers of importance for successful thrombolysis

Full Information

First Posted
November 9, 2005
Last Updated
April 29, 2015
Sponsor
Oslo University Hospital
Collaborators
Ostfold Hospital Trust
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1. Study Identification

Unique Protocol Identification Number
NCT00251771
Brief Title
Catheter-Directed Venous Thrombolysis in Acute Iliofemoral Vein Thrombosis
Acronym
CaVenT
Official Title
Catheter-directed Venous Thrombolysis in Acute Iliofemoral Vein Thrombosis, an Open Randomized, Controlled, Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Oslo University Hospital
Collaborators
Ostfold Hospital Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Deep vein thrombosis (DVT) is a severe disease, and conventional treatment with low molecular weight heparin (LMWH) and warfarin is associated with some degree of long-term sequelae, i.e. post-thrombotic syndrome (PTS). Catheter-directed thrombolytic (CDT) therapy has been introduced worldwide the last two decades. Reports have suggested a beneficial effect of this costly treatment, but there are no randomized clinical trials documenting its short- and long-term efficacy and safety. This multi-center study will randomize patients with acute iliofemoral vein thrombosis to either conventional treatment or CDT in addition to conventional treatment. Main outcome parameters are patency rates at 6 months and prevalence of PTS at 24 months. The main short-term hypothesis is that CDT of first-time acute DVT will increase patency of the affected segments after 6 months from <50% to >80%. The main long-term hypothesis is that CDT will improve long-term functional outcome, i.e. risk of PTS after 2 years from >25% to <10%.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis
Keywords
Thrombolytic therapy, Postphlebitic syndrome, Venous thrombosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
209 (Actual)

8. Arms, Groups, and Interventions

Arm Title
I
Arm Type
Experimental
Arm Title
II
Arm Type
No Intervention
Intervention Type
Procedure
Intervention Name(s)
catheter-directed venous thrombolysis
Intervention Description
catheter-directed continuous intravenous infusion of alteplase 0.01mg/kg/h and low-dose heparin. Max dose 20mg/24 h and up to 96 hrs.
Primary Outcome Measure Information:
Title
Patency after 6 months
Time Frame
6 months
Title
Post-thrombotic syndrome after 2 years (yrs)
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Frequency of clinically relevant bleeding complications
Time Frame
1 year
Title
Effects on quality of life
Time Frame
2 and 5 years
Title
Cost-effectiveness of treatment
Time Frame
2 years
Title
Procedural success of CDT
Time Frame
1 week
Title
Patency at 2 years
Time Frame
2 years
Title
PTS at 6, 12, 36, 48 and 60 months
Time Frame
6, 12, 36, 48 and 60 months
Title
Relation between PTS and patency
Time Frame
2 years
Title
Prevalence of vein anomalies
Time Frame
6 months
Title
Prevalence of underlying thrombophilia
Time Frame
1 year
Title
Frequency of recurrent venous thrombotic events (VTE)
Time Frame
0.5, 2 and 5 years
Title
Markers of importance for recurrent thrombosis
Time Frame
0.5, 2 and 5 years
Title
Markers of importance for successful thrombolysis
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Onset of symptoms <21 days Objectively verified DVT of the femoral or common iliac veins or the combined iliofemoral segment Informed consent Exclusion Criteria: Anticoagulant therapy prior to trial entry >7 days Contraindications to thrombolytic therapy Indications for thrombolytic therapy, i.e. phlegmasia coerulea dolens or vena cava thrombosis Severe anemia, hemoglobin (hgb)<8 g/dl Thrombocytopenia, platelets <80x10^9/l Severe renal failure, creatinine clearance <30ml/min Severe hypertension, systolic (syst) blood pressure (BP)>160 mmHg or diastolic (diast) BP >100 mmHg pregnancy Less than 14 days post-surgery or post-trauma History of subarachnoidal or intracerebral bleeding Disease with life expectancy <24 months Drug abuse or mental disease that may interfere with treatment and follow-up Former ipsilateral proximal DVT Chemotherapy or advanced malignant disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Per Morten Sandset, MD
Organizational Affiliation
Ullevaal University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Ullevaal University Hospital
City
Oslo
ZIP/Postal Code
0407
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
16794675
Citation
Enden T, Klow NE, Sandset PM. [Catheter-directed thrombolysis in acute deep venous thrombosis]. Tidsskr Nor Laegeforen. 2006 Jun 22;126(13):1765. No abstract available. Norwegian.
Results Reference
background
PubMed Identifier
17967583
Citation
Enden T, Sandvik L, Klow NE, Hafsahl G, Holme PA, Holmen LO, Ghanima W, Njaastad AM, Sandbaek G, Slagsvold CE, Sandset PM. Catheter-directed Venous Thrombolysis in acute iliofemoral vein thrombosis--the CaVenT study: rationale and design of a multicenter, randomized, controlled, clinical trial (NCT00251771). Am Heart J. 2007 Nov;154(5):808-14. doi: 10.1016/j.ahj.2007.07.010. Epub 2007 Sep 6.
Results Reference
background
PubMed Identifier
19068041
Citation
Enden T, Garratt AM, Klow NE, Sandset PM. Assessing burden of illness following acute deep vein thrombosis: data quality, reliability and validity of the Norwegian version of VEINES-QOL/Sym, a disease-specific questionnaire. Scand J Caring Sci. 2009 Jun;23(2):369-74. doi: 10.1111/j.1471-6712.2008.00618.x. Epub 2008 Nov 12.
Results Reference
background
PubMed Identifier
22669381
Citation
Enden T, Sandset PM, Klow NE. Evidence-based practice for patients with severe venous thrombosis. Tidsskr Nor Laegeforen. 2012 May 29;132(10):1215-6. doi: 10.4045/tidsskr.12.0474. No abstract available. English, Norwegian.
Results Reference
background
PubMed Identifier
19422443
Citation
Enden T, Klow NE, Sandvik L, Slagsvold CE, Ghanima W, Hafsahl G, Holme PA, Holmen LO, Njaastad AM, Sandbaek G, Sandset PM; CaVenT study group. Catheter-directed thrombolysis vs. anticoagulant therapy alone in deep vein thrombosis: results of an open randomized, controlled trial reporting on short-term patency. J Thromb Haemost. 2009 Aug;7(8):1268-75. doi: 10.1111/j.1538-7836.2009.03464.x. Epub 2009 Apr 30.
Results Reference
result
PubMed Identifier
22172244
Citation
Enden T, Haig Y, Klow NE, Slagsvold CE, Sandvik L, Ghanima W, Hafsahl G, Holme PA, Holmen LO, Njaastad AM, Sandbaek G, Sandset PM; CaVenT Study Group. Long-term outcome after additional catheter-directed thrombolysis versus standard treatment for acute iliofemoral deep vein thrombosis (the CaVenT study): a randomised controlled trial. Lancet. 2012 Jan 7;379(9810):31-8. doi: 10.1016/S0140-6736(11)61753-4. Epub 2011 Dec 13.
Results Reference
result
PubMed Identifier
23176966
Citation
Haig Y, Enden T, Slagsvold CE, Sandvik L, Sandset PM, Klow NE. Determinants of early and long-term efficacy of catheter-directed thrombolysis in proximal deep vein thrombosis. J Vasc Interv Radiol. 2013 Jan;24(1):17-24; quiz 26. doi: 10.1016/j.jvir.2012.09.023. Epub 2012 Nov 22.
Results Reference
result
PubMed Identifier
23452204
Citation
Enden T, Resch S, White C, Wik HS, Klow NE, Sandset PM. Cost-effectiveness of additional catheter-directed thrombolysis for deep vein thrombosis. J Thromb Haemost. 2013 Jun;11(6):1032-42. doi: 10.1111/jth.12184.
Results Reference
result
PubMed Identifier
23988361
Citation
Enden T, Wik HS, Kvam AK, Haig Y, Klow NE, Sandset PM. Health-related quality of life after catheter-directed thrombolysis for deep vein thrombosis: secondary outcomes of the randomised, non-blinded, parallel-group CaVenT study. BMJ Open. 2013 Aug 29;3(8):e002984. doi: 10.1136/bmjopen-2013-002984.
Results Reference
result
PubMed Identifier
24082798
Citation
Enden T, Klow NE, Sandset PM. Symptom burden and job absenteeism after treatment with additional catheter-directed thrombolysis for deep vein thrombosis. Patient Relat Outcome Meas. 2013 Sep 16;4:55-9. doi: 10.2147/PROM.S47233. eCollection 2013.
Results Reference
result
PubMed Identifier
33464575
Citation
Broderick C, Watson L, Armon MP. Thrombolytic strategies versus standard anticoagulation for acute deep vein thrombosis of the lower limb. Cochrane Database Syst Rev. 2021 Jan 19;1(1):CD002783. doi: 10.1002/14651858.CD002783.pub5.
Results Reference
derived
PubMed Identifier
26853645
Citation
Haig Y, Enden T, Grotta O, Klow NE, Slagsvold CE, Ghanima W, Sandvik L, Hafsahl G, Holme PA, Holmen LO, Njaaastad AM, Sandbaek G, Sandset PM; CaVenT Study Group. Post-thrombotic syndrome after catheter-directed thrombolysis for deep vein thrombosis (CaVenT): 5-year follow-up results of an open-label, randomised controlled trial. Lancet Haematol. 2016 Feb;3(2):e64-71. doi: 10.1016/S2352-3026(15)00248-3. Epub 2016 Jan 6.
Results Reference
derived

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Catheter-Directed Venous Thrombolysis in Acute Iliofemoral Vein Thrombosis

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