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Single Session Percutaneous Mechanical Thrombectomy for the Treatment of Ilio-femoral Deep Vein Thrombosis: A Preliminary Evaluation (SPADE)

Primary Purpose

Deep Vein Thrombosis, Venous Thromboembolism

Status
Terminated
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Thrombectomy
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Deep Vein Thrombosis focused on measuring Deep vein thrombosis, thrombectomy, percutaneuos

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers
  1. objectively diagnosed IFDVT
  2. symptom duration < 14 days for the DVT episode in the index leg at the time of enrolment
  3. age > 18 years

Exclusion criteria:

  1. indications for thrombolytic therapy (i.e. phlegmasia cerulean dolens)
  2. pregnancy
  3. life expectancy < 6 months
  4. severe kidney disease (creatinine clearance < 30 mL min)
  5. refusal to provide informed consent or inability to follow up
  6. allergy to contrast media
  7. the lesion cannot be accessed with the wire guide
  8. prior history of ipsilateral DVT or femoral catheters

Sites / Locations

  • Ottawa Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention

Arm Description

Outcomes

Primary Outcome Measures

angiographic luminal patency
The main outcome of the study will be the percentage of patients who achieve an angiographic luminal patency > 50% at the end of the procedure without the need of adjuvant CDT. Luminal patency will be calculated using the thrombus score for seven venous segments. The thrombus score is 0 when the vein was patent and completely free of thrombus, 1 when partially occluded, and 2 when completely occluded. The total thrombus score will be then calculated by adding the scores of the seven venous segments before and after PMT. The difference between the pre- and post-PMT thrombus scores divided by the pre-PMT score will result in the percentage of luminal patency, classified into three groups for analysis: grade I less than 50%, grade II 50%-99%, and grade III for 100%.

Secondary Outcome Measures

Recurrent VTE
Acute symptomatic recurrent DVT or PE
Patency
Patency of the treated segment on ultrasound.
Bleeding
Major, clinically relevant and minor peri-procedural bleeding within 7 days and 3 months
PTS using Villalta score
Hemolyisis
Quality of Life
Quality of life at the end of follow up is measured using the VEINES-QOL/Sym score
Procedure associated complications

Full Information

First Posted
November 5, 2013
Last Updated
April 15, 2015
Sponsor
Ottawa Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02066597
Brief Title
Single Session Percutaneous Mechanical Thrombectomy for the Treatment of Ilio-femoral Deep Vein Thrombosis: A Preliminary Evaluation
Acronym
SPADE
Official Title
Single Session Percutaneous Mechanical Thrombectomy for the Treatment of Ilio-femoral Deep Vein Thrombosis: A Preliminary Evaluation
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Terminated
Why Stopped
Recommendation from the DSMB following recurrent DVT in 3/4 participants who underwent the thrombectomy procedure.
Study Start Date
November 2013 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Hospital Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Venous thromboembolism (VTE) is a common condition that occurs when a clot develops in one of your veins. It affects 5% of the population and is the third most common circulatory condition after heart attack and stroke. People who experience a clot in their vein can have significant long term problems with swelling and discomfort. The investigators call this post thrombotic syndrome (PTS). They can also be at increased risk of having another clot occur. People who have ilio-femoral clots are more likely to have more severe leg swelling and pain than those who have clots in smaller veins. They are also more likely to have problems returning to their normal daily routines and may need more hospital visits. The current standard of care involves treating patients with anticoagulants (blood thinners) because it has a low risk of bleeding risk and is inexpensive. Blood thinners prevent the clot from growing bigger while your own body dissolves the clot over time. The type of clot you have is the most severe form of DVT. Some experts advise early removal of the clot - resulting in symptom relief sooner and possibly reducing the risk of PTS. This is in addition to the standard treatment with blood thinners. There are currently two options for physically removing these clots. One method involves placing an intravenous catheter into your leg and injecting medication directly where the clot is situated. This dissolves the clot. This method is called Catheter Directed Thrombolysis (CDT). The second method, Percutaneous Mechanical Thrombectomy (PMT), involves placing an intravenous catheter into your leg and breaking down the clot mechanically and suctioning it out of the vein - creating good blood flow again to your leg. Both methods require injection of contrast dye and a special x-ray machine to see where the clot is and ensure that the entire clot is removed. CDT is very expensive and has an increased risk of major bleeding. PMT is much less expensive and has a lower risk of bleeding. The doctors at The Ottawa Hospital do not typically recommend CDT, nor do we commonly perform PMT for this patient population here. The investigators would like to enroll 26 participants with ilio-femoral DVTs and perform PMT to see if they can achieve better outcomes than for those who have just had our routine treatment of blood thinners. The investigators are only conducting this study here at The Ottawa Hospital, General Campus. They will follow the progress of participants for 6 months. The device the investigators are using (Angiojet Ultra Thrombectomy System) is already approved by Health Canada for this procedure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis, Venous Thromboembolism
Keywords
Deep vein thrombosis, thrombectomy, percutaneuos

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Thrombectomy
Intervention Description
Within 96 hours of enrolment, patients will be treated with a single session of PMT using an AngioJet catheter without adjuvant thrombolysis . Venous access will be obtained at the popliteal vein in all patients with a 5-F sheath through which all subsequent venography procedures will be performed. The AngioJet catheter will then be passed over the guide wire and moved from proximal to distal to remove thrombus. Completion venography will be performed through the sheath in all patients. After the completion of the procedure patients are expected to remain in hospital for no more than six hours (1 hour in post-anaesthesia care unit followed by transfer to the surgical daycare unit from where they will be discharged).
Primary Outcome Measure Information:
Title
angiographic luminal patency
Description
The main outcome of the study will be the percentage of patients who achieve an angiographic luminal patency > 50% at the end of the procedure without the need of adjuvant CDT. Luminal patency will be calculated using the thrombus score for seven venous segments. The thrombus score is 0 when the vein was patent and completely free of thrombus, 1 when partially occluded, and 2 when completely occluded. The total thrombus score will be then calculated by adding the scores of the seven venous segments before and after PMT. The difference between the pre- and post-PMT thrombus scores divided by the pre-PMT score will result in the percentage of luminal patency, classified into three groups for analysis: grade I less than 50%, grade II 50%-99%, and grade III for 100%.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Recurrent VTE
Description
Acute symptomatic recurrent DVT or PE
Time Frame
3 months
Title
Patency
Description
Patency of the treated segment on ultrasound.
Time Frame
Seven days and 3 months
Title
Bleeding
Description
Major, clinically relevant and minor peri-procedural bleeding within 7 days and 3 months
Time Frame
3 months
Title
PTS using Villalta score
Time Frame
3 months
Title
Hemolyisis
Time Frame
7 days
Title
Quality of Life
Description
Quality of life at the end of follow up is measured using the VEINES-QOL/Sym score
Time Frame
3 months
Title
Procedure associated complications
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
objectively diagnosed IFDVT symptom duration < 14 days for the DVT episode in the index leg at the time of enrolment age > 18 years Exclusion criteria: indications for thrombolytic therapy (i.e. phlegmasia cerulean dolens) pregnancy life expectancy < 6 months severe kidney disease (creatinine clearance < 30 mL min) refusal to provide informed consent or inability to follow up allergy to contrast media the lesion cannot be accessed with the wire guide prior history of ipsilateral DVT or femoral catheters
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Esteban Gandara, MD
Organizational Affiliation
OHRI
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Single Session Percutaneous Mechanical Thrombectomy for the Treatment of Ilio-femoral Deep Vein Thrombosis: A Preliminary Evaluation

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