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Standard Open Surgery Versus Endovascular Repair of Abdominal Aortic Aneurysm (AAA) (OVER)

Primary Purpose

Aortic Aneurysm

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Endovascular Repair
Standard Open Repair
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aortic Aneurysm focused on measuring Abdominal, Aortic Aneurysm, cost of AAA repair, Endovascular Repair, Grafts, Long-term survival, secondary outcomes

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: AAA with a maximum external diameter in any plane greater than or equal to 5 cm. An iliac aneurysm (associated with an AAA) with a maximum external diameter in any plane greater than or equal to 3 cm. AAA greater than or equal to 4.5 cm and the AAA has increased by greater than or equal to 0.7 cm in diameter in 6 months. An AAA greater than or equal to 4.5 cm and the AAA has increased by greater than or equal to 1 cm in diameter in 12 months. An AAA greater than or equal to 4.5 cm and the AAA is saccular (i.e., a portion of the circumference of the aorta at the level of the aneurysm is considered normal based on CT scan or MRI). An AAA greater than or equal to 4.5 cm and the AAA is associated with distal embolism. as measured from two imaging studies (ultrasound CT scan or MRI) within the appropriate interval, the later one within 6 months of randomization. Exclusion Criteria: Patient has had a previous AAA repair procedure Evidence of AAA rupture by imaging test AAA is not elective (i.e., urgent or emergent operation, usually due to suspected rupture) Likelihood of poor compliance to the protocol Patient refused randomization Physician refused randomization

Sites / Locations

  • VA Medical Center, Birmingham
  • Southern Arizona VA Health Care System, Tucson
  • Central Arkansas VHS Eugene J. Towbin Healthcare Ctr, Little Rock
  • VA Medical Center, Loma Linda
  • VA Medical Center, Long Beach
  • VA Palo Alto Health Care System
  • VA San Diego Healthcare System, San Diego
  • VA Medical Center, San Francisco
  • VA Greater Los Angeles Healthcare System, West LA
  • VA Eastern Colorado Health Care System, Denver
  • VA Connecticut Health Care System (West Haven)
  • VA Medical Center, DC
  • North Florida/South Georgia Veterans Health System
  • James A. Haley Veterans Hospital, Tampa
  • Atlanta VA Medical and Rehab Center, Decatur
  • Jesse Brown VAMC (WestSide Division)
  • Edward Hines, Jr. VA Hospital
  • Richard Roudebush VA Medical Center, Indianapolis
  • VA Medical Center, Iowa City
  • VA Medical Center, Lexington
  • VA Maryland Health Care System, Baltimore
  • VA Boston Healthcare System, Brockton Campus
  • John D. Dingell VA Medical Center, Detroit
  • Minneapolis VA Health Care System
  • VA Medical Center, Omaha
  • VA New Jersey Health Care System, East Orange
  • New Mexico VA Health Care System, Albuquerque
  • VA Western New York Healthcare System at Buffalo
  • New York Harbor HCS
  • VA Medical Center, Durham
  • VA Medical Center, Cincinnati
  • VA Medical Center, Cleveland
  • VA Medical Center, Portland
  • VA Medical Center, Philadelphia
  • VA Pittsburgh Health Care System
  • VA Medical Center, Memphis
  • VA North Texas Health Care System, Dallas
  • Michael E. DeBakey VA Medical Center (152)
  • VA Salt Lake City Health Care System, Salt Lake City
  • VA Puget Sound Health Care System, Seattle
  • Wlliam S. Middleton Memorial Veterans Hospital, Madison
  • Zablocki VA Medical Center, Milwaukee

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Arm 1

Arm 2

Arm Description

Standard Open Repair of Abdominal Aortic Aneurysm

Endovascular Repair of Abdominal Aortic Aneurysm

Outcomes

Primary Outcome Measures

All-cause Mortality
Participants vital status was assessed from randomization to end of study follow-up [10/15/2011] or death [whichever occurred first].

Secondary Outcome Measures

Secondary Therapeutic Procedures
This outcome includes any procedure that resulted directly or indirectly from the initial procedure and that required a separate trip to the procedure suite (with each trip to the procedure suite counting as one secondary procedure), including any unplanned surgical procedures within 30 days after the initial procedure and any additional aortoiliac procedures at any time.
SF-36 Mental Component Score (MCS)
Change (over time) since baseline in Mental Component Score of SF-36. The MCS Score ranges from 0-100 with higher scores indicating better health. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
SF-36 Physical Component Score (PCS)
Change (over time) since baseline in Physical Component Score of SF-36. The PCS Score ranges from 0-100 with higher scores indicating better health Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
SF-36 Physical Component Deaths Included Score (PCTD)
Change (over time) since baseline in Physical Component Deaths included Score of SF-36. The PCTD Score ranges from 0-100 with higher scores indicating better health. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
European Quality of Life-5 Dimension (EQ-5D) Index Score
Change (over time) since baseline in EQ-5D. The EQ-5D Index Score ('thermometer scale') ranges from 0 (worst health status) to 100 (best health status). Since this outcome captures change since baseline, values could be below 0. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
European Quality of Life-5 Dimension (EQ-5D) Visual Analog Scale
Change (over time) since baseline in EQ-5D Visual Analog Scale. The EQ-5D Visual Analog Scale ranges from 0 (death) to 1 (perfect health). Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
International Index of Erectile Function (IIEF-5)
Change (over time) since baseline in IIEF-5. The IIEF-5 Score ranges from 5-25 with higher scores indicating better erectile function. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.

Full Information

First Posted
October 20, 2004
Last Updated
February 8, 2016
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT00094575
Brief Title
Standard Open Surgery Versus Endovascular Repair of Abdominal Aortic Aneurysm (AAA)
Acronym
OVER
Official Title
CSP #498 - Open Versus Endovascular Repair (OVER) Trial for Abdominal Aortic Aneurysms
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
October 2002 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
April 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A multi-center, randomized clinical trial that will compare endovascular repair with standard open surgery in the repair of abdominal aortic aneurysms (AAA). Long and short-term results as well as the cost and quality of life associated with these two strategies for AAA repair will be compared.
Detailed Description
Primary Hypothesis: All-cause mortality will differ by 25% between Endovascular repair (EVR) and Open repair. Secondary Hypotheses: Procedure failure, short term (12-month) major morbidity, number of hospital days, health-related quality of life and other procedure-related abnormalities will differ between the two AAA repair strategies. Primary Outcomes: All-cause mortality. Interventions: Patients will be randomized to one of these repair strategies for the elective treatment of AAA: (a) Open repair or (b) Endovascular repair (using FDA-approved devices). Study Abstract: Aortic aneurysm is the tenth leading cause of death in older men; AAA accounts for the majority of these deaths (about 10,000 deaths per year in the United States). Since one in 22 Veterans over the age of 50 have AAA and one in 200 have AAA with diameter greater or equal to 5.0 cm (making them candidates for elective repair), AAA is a major disease in the VA population. Questions about the relative safety and effectiveness of FDA approved EVR devices have been raised and remain unanswered. To answer these questions, this multi-center, randomized clinical trial comparing EVR with standard open surgery is proposed. Patients for whom elective repair of AAA is indicated and who are suitable candidates for both open repair and EVR will be eligible for the study. The anticipated duration of the study is 9 years with a proposed sample size of 900 patients. The first planning meeting took place on March 9-10, 2000 and the second planning meeting took place on November 6-7, 2000. The OVER protocol was submitted and reviewed by CSEC on May 10, 2001 and approved. The kickoff was June 12, 2002. The first DSMB meeting took place January 6, 2003. First annual meeting was held September 30, 2003; second DSMB meeting took place September 29, 2003. Third DSMB meeting held on April 19, 2004; second annual meeting was held on June 29, 2004. Fourth DSMB meeting was held on December 6, 2004; third annual meeting was held on March 15, 2005. The fifth DSMB meeting was held on July 19, 2005 and the fourth annual meeting was held March 21, 2006. The sixth DSMB meeting was held September 12, 2005. The seventh DSMB meeting was held on March 6, 2006. The eighth DSMB meeting was held on November 6, 2006. At its November 6, 2006 meeting, the DSMB discussed and approved unblinding of the study chair to prepare the short-term follow-up paper as specified in the study protocol. Initially the protocol called for this analysis to include one-year follow-up data. After discussions with the Trial Leadership, the DSMB approved use of two year follow-up data (reflected in DSMB minutes finalized February 20, 2007). This recommendation was subsequently approved by CSP in March 2007. The short-term outcomes manuscript was published in JAMA on October 14, 2009. The ninth DSMB meeting was held on May 14, 2007 and the fifth annual meeting was held on June 6, 2007. The tenth DSMB meeting was held on April 7, 2008. The eleventh DMC (name change only from DSMB to DMC) was held on June 22, 2009. The twelfth DMC meeting was held on May 24, 2010. A Site Investigator meeting was held in Boston, MA on June 9, 2010. The thirteenth DMC meeting was held on June 3, 2011 and a study close-out meeting was held on June 15, 2011 in Chicago, IL. The study's patient follow-up phase ended October 15, 2011.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Aneurysm
Keywords
Abdominal, Aortic Aneurysm, cost of AAA repair, Endovascular Repair, Grafts, Long-term survival, secondary outcomes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
881 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Active Comparator
Arm Description
Standard Open Repair of Abdominal Aortic Aneurysm
Arm Title
Arm 2
Arm Type
Active Comparator
Arm Description
Endovascular Repair of Abdominal Aortic Aneurysm
Intervention Type
Procedure
Intervention Name(s)
Endovascular Repair
Intervention Description
Endovascular Repair
Intervention Type
Procedure
Intervention Name(s)
Standard Open Repair
Intervention Description
Standard Open Repair
Primary Outcome Measure Information:
Title
All-cause Mortality
Description
Participants vital status was assessed from randomization to end of study follow-up [10/15/2011] or death [whichever occurred first].
Time Frame
Participants were followed for the duration of the study, up to 9 years
Secondary Outcome Measure Information:
Title
Secondary Therapeutic Procedures
Description
This outcome includes any procedure that resulted directly or indirectly from the initial procedure and that required a separate trip to the procedure suite (with each trip to the procedure suite counting as one secondary procedure), including any unplanned surgical procedures within 30 days after the initial procedure and any additional aortoiliac procedures at any time.
Time Frame
Participants were followed for the duration of the study, up to 9 years
Title
SF-36 Mental Component Score (MCS)
Description
Change (over time) since baseline in Mental Component Score of SF-36. The MCS Score ranges from 0-100 with higher scores indicating better health. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
Time Frame
Outcome was assessed at 6 months and then yearly, up to 9 years
Title
SF-36 Physical Component Score (PCS)
Description
Change (over time) since baseline in Physical Component Score of SF-36. The PCS Score ranges from 0-100 with higher scores indicating better health Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
Time Frame
Outcome was assessed at 6 months and yearly thereafter, up to 9 years
Title
SF-36 Physical Component Deaths Included Score (PCTD)
Description
Change (over time) since baseline in Physical Component Deaths included Score of SF-36. The PCTD Score ranges from 0-100 with higher scores indicating better health. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
Time Frame
Outcome was assessed at 6 months and yearly thereafter, up to 9 years
Title
European Quality of Life-5 Dimension (EQ-5D) Index Score
Description
Change (over time) since baseline in EQ-5D. The EQ-5D Index Score ('thermometer scale') ranges from 0 (worst health status) to 100 (best health status). Since this outcome captures change since baseline, values could be below 0. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
Time Frame
Outcome was assessed at 6 months and yearly thereafter, up to 9 years
Title
European Quality of Life-5 Dimension (EQ-5D) Visual Analog Scale
Description
Change (over time) since baseline in EQ-5D Visual Analog Scale. The EQ-5D Visual Analog Scale ranges from 0 (death) to 1 (perfect health). Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
Time Frame
Outcome was assessed at 6 months and yearly thereafter, up to 9 years
Title
International Index of Erectile Function (IIEF-5)
Description
Change (over time) since baseline in IIEF-5. The IIEF-5 Score ranges from 5-25 with higher scores indicating better erectile function. Longitudinal mixed-effects model, adjusted for baseline values, was used to compare the two study arms. Treatment effect and change in quality-of-life measures over time were assessed in repeated measures models (with unstructured covariance) with the assigned repair method and baseline measurements used as covariates. Least-squares mean changes from baseline were calculated at each time point; the reported overall least squares mean is calculated over all time points.
Time Frame
Outcome was assessed at 6 months and yearly thereafter, up to 9 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: AAA with a maximum external diameter in any plane greater than or equal to 5 cm. An iliac aneurysm (associated with an AAA) with a maximum external diameter in any plane greater than or equal to 3 cm. AAA greater than or equal to 4.5 cm and the AAA has increased by greater than or equal to 0.7 cm in diameter in 6 months. An AAA greater than or equal to 4.5 cm and the AAA has increased by greater than or equal to 1 cm in diameter in 12 months. An AAA greater than or equal to 4.5 cm and the AAA is saccular (i.e., a portion of the circumference of the aorta at the level of the aneurysm is considered normal based on CT scan or MRI). An AAA greater than or equal to 4.5 cm and the AAA is associated with distal embolism. as measured from two imaging studies (ultrasound CT scan or MRI) within the appropriate interval, the later one within 6 months of randomization. Exclusion Criteria: Patient has had a previous AAA repair procedure Evidence of AAA rupture by imaging test AAA is not elective (i.e., urgent or emergent operation, usually due to suspected rupture) Likelihood of poor compliance to the protocol Patient refused randomization Physician refused randomization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank A. Lederle, MD
Organizational Affiliation
Minneapolis Veterans Affairs Medical Center
Official's Role
Study Chair
Facility Information:
Facility Name
VA Medical Center, Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Southern Arizona VA Health Care System, Tucson
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85723
Country
United States
Facility Name
Central Arkansas VHS Eugene J. Towbin Healthcare Ctr, Little Rock
City
No. Little Rock
State/Province
Arkansas
ZIP/Postal Code
72114-1706
Country
United States
Facility Name
VA Medical Center, Loma Linda
City
Loma Linda
State/Province
California
ZIP/Postal Code
92357
Country
United States
Facility Name
VA Medical Center, Long Beach
City
Long Beach
State/Province
California
ZIP/Postal Code
90822
Country
United States
Facility Name
VA Palo Alto Health Care System
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304-1290
Country
United States
Facility Name
VA San Diego Healthcare System, San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92161
Country
United States
Facility Name
VA Medical Center, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94121
Country
United States
Facility Name
VA Greater Los Angeles Healthcare System, West LA
City
West Los Angeles
State/Province
California
ZIP/Postal Code
90073
Country
United States
Facility Name
VA Eastern Colorado Health Care System, Denver
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
Facility Name
VA Connecticut Health Care System (West Haven)
City
West Haven
State/Province
Connecticut
ZIP/Postal Code
06516
Country
United States
Facility Name
VA Medical Center, DC
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20422
Country
United States
Facility Name
North Florida/South Georgia Veterans Health System
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32608
Country
United States
Facility Name
James A. Haley Veterans Hospital, Tampa
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Name
Atlanta VA Medical and Rehab Center, Decatur
City
Decatur
State/Province
Georgia
ZIP/Postal Code
30033
Country
United States
Facility Name
Jesse Brown VAMC (WestSide Division)
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
Edward Hines, Jr. VA Hospital
City
Hines
State/Province
Illinois
ZIP/Postal Code
60141-5000
Country
United States
Facility Name
Richard Roudebush VA Medical Center, Indianapolis
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202-2884
Country
United States
Facility Name
VA Medical Center, Iowa City
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52246-2208
Country
United States
Facility Name
VA Medical Center, Lexington
City
Lexington
State/Province
Kentucky
ZIP/Postal Code
40502
Country
United States
Facility Name
VA Maryland Health Care System, Baltimore
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Facility Name
VA Boston Healthcare System, Brockton Campus
City
Brockton
State/Province
Massachusetts
ZIP/Postal Code
02301
Country
United States
Facility Name
John D. Dingell VA Medical Center, Detroit
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Minneapolis VA Health Care System
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55417
Country
United States
Facility Name
VA Medical Center, Omaha
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68105-1873
Country
United States
Facility Name
VA New Jersey Health Care System, East Orange
City
East Orange
State/Province
New Jersey
ZIP/Postal Code
07018
Country
United States
Facility Name
New Mexico VA Health Care System, Albuquerque
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87108-5153
Country
United States
Facility Name
VA Western New York Healthcare System at Buffalo
City
Buffalo
State/Province
New York
ZIP/Postal Code
14215
Country
United States
Facility Name
New York Harbor HCS
City
New York
State/Province
New York
ZIP/Postal Code
10010
Country
United States
Facility Name
VA Medical Center, Durham
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705
Country
United States
Facility Name
VA Medical Center, Cincinnati
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45220
Country
United States
Facility Name
VA Medical Center, Cleveland
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
VA Medical Center, Portland
City
Portland
State/Province
Oregon
ZIP/Postal Code
97201
Country
United States
Facility Name
VA Medical Center, Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
VA Pittsburgh Health Care System
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15240
Country
United States
Facility Name
VA Medical Center, Memphis
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38104
Country
United States
Facility Name
VA North Texas Health Care System, Dallas
City
Dallas
State/Province
Texas
ZIP/Postal Code
75216
Country
United States
Facility Name
Michael E. DeBakey VA Medical Center (152)
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
VA Salt Lake City Health Care System, Salt Lake City
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84148
Country
United States
Facility Name
VA Puget Sound Health Care System, Seattle
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States
Facility Name
Wlliam S. Middleton Memorial Veterans Hospital, Madison
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53705
Country
United States
Facility Name
Zablocki VA Medical Center, Milwaukee
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53295-1000
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19773791
Citation
Lederle FA. Vascular disease: is AAA screening worth the cost? Nat Rev Cardiol. 2009 Oct;6(10):616-8. doi: 10.1038/nrcardio.2009.161. No abstract available.
Results Reference
result
PubMed Identifier
19826022
Citation
Lederle FA, Freischlag JA, Kyriakides TC, Padberg FT Jr, Matsumura JS, Kohler TR, Lin PH, Jean-Claude JM, Cikrit DF, Swanson KM, Peduzzi PN; Open Versus Endovascular Repair (OVER) Veterans Affairs Cooperative Study Group. Outcomes following endovascular vs open repair of abdominal aortic aneurysm: a randomized trial. JAMA. 2009 Oct 14;302(14):1535-42. doi: 10.1001/jama.2009.1426.
Results Reference
result
Citation
Lederle FA, Freischlag JA, Kyriakides TC. Comparing endovascular and open repair of abdominal aortic aneurysm - [Author Reply To Editorial]. Journal of The American Medical Association. 2010 Feb 10; 303(6):514.
Results Reference
result
PubMed Identifier
21900095
Citation
Lederle FA. The rise and fall of abdominal aortic aneurysm. Circulation. 2011 Sep 6;124(10):1097-9. doi: 10.1161/CIRCULATIONAHA.111.052365. No abstract available.
Results Reference
result
PubMed Identifier
22237512
Citation
Lederle FA. The strange relationship between diabetes and abdominal aortic aneurysm. Eur J Vasc Endovasc Surg. 2012 Mar;43(3):254-6. doi: 10.1016/j.ejvs.2011.12.026. Epub 2012 Jan 9.
Results Reference
result
PubMed Identifier
22640466
Citation
Stroupe KT, Lederle FA, Matsumura JS, Kyriakides TC, Jonk YC, Ge L, Freischlag JA; Open Versus Endovascular Repair (OVER) Veterans Affairs Cooperative Study Group. Cost-effectiveness of open versus endovascular repair of abdominal aortic aneurysm in the OVER trial. J Vasc Surg. 2012 Oct;56(4):901-9.e2. doi: 10.1016/j.jvs.2012.01.086. Epub 2012 May 27.
Results Reference
result
PubMed Identifier
23171095
Citation
Lederle FA, Freischlag JA, Kyriakides TC, Matsumura JS, Padberg FT Jr, Kohler TR, Kougias P, Jean-Claude JM, Cikrit DF, Swanson KM; OVER Veterans Affairs Cooperative Study Group. Long-term comparison of endovascular and open repair of abdominal aortic aneurysm. N Engl J Med. 2012 Nov 22;367(21):1988-97. doi: 10.1056/NEJMoa1207481.
Results Reference
result
PubMed Identifier
23116986
Citation
Lederle FA, Stroupe KT; Open Versus Endovascular Repair (OVER) Veterans Affairs Cooperative Study Group. Cost-effectiveness at two years in the VA Open Versus Endovascular Repair Trial. Eur J Vasc Endovasc Surg. 2012 Dec;44(6):543-8. doi: 10.1016/j.ejvs.2012.10.002. Epub 2012 Oct 30.
Results Reference
result
PubMed Identifier
24490269
Citation
Lederle FA. Abdominal aortic aneurysm: still no pill. Ann Intern Med. 2013 Dec 17;159(12):852-3. doi: 10.7326/0003-4819-159-12-201312170-00012. No abstract available.
Results Reference
result
PubMed Identifier
26598115
Citation
Lal BK, Zhou W, Li Z, Kyriakides T, Matsumura J, Lederle FA, Freischlag J; OVER Veterans Affairs Cooperative Study Group. Predictors and outcomes of endoleaks in the Veterans Affairs Open Versus Endovascular Repair (OVER) Trial of Abdominal Aortic Aneurysms. J Vasc Surg. 2015 Dec;62(6):1394-404. doi: 10.1016/j.jvs.2015.02.003.
Results Reference
result
PubMed Identifier
31141634
Citation
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Standard Open Surgery Versus Endovascular Repair of Abdominal Aortic Aneurysm (AAA)

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