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Ultra-sound for AAA Screening in Smoking Israeli Arab Men

Primary Purpose

Abdominal Aortic Aneurysm (AAA)

Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Duplex ultra sound screening for abdominal aortic aneurysms
Sponsored by
Clalit Health Services
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Abdominal Aortic Aneurysm (AAA) focused on measuring Abdominal aortic aneurysm, Abdominal aortic aneurism, AAA, Screening, duplex ultra sound, Israeli Arab men, family physician

Eligibility Criteria

60 Years - 80 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Arab men
  • Age : 60-80 years old
  • History of smoking

Exclusion Criteria:

  • A known AAA
  • Previous operations of the abdominal aorta
  • Previous imaging study within the last 12 months, ruling-out AAA.

Sites / Locations

  • Clalit Health Services primary clinics

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Israeli Arab men

Arm Description

Single arm study. The arm includes all enrolled patients screened by duplex ultra sound for abdominal aortic aneurysms.

Outcomes

Primary Outcome Measures

Abdominal aortic aneurysm prevalence in the represented population
At the end of enrollment, estimated time - 2 years, the prevalence will be assessed.

Secondary Outcome Measures

Full Information

First Posted
November 26, 2014
Last Updated
February 7, 2017
Sponsor
Clalit Health Services
Collaborators
Medtronic
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1. Study Identification

Unique Protocol Identification Number
NCT02306304
Brief Title
Ultra-sound for AAA Screening in Smoking Israeli Arab Men
Official Title
Ultra-sound for AAA Screening in Smoking Israeli Arab Men
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
January 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Clalit Health Services
Collaborators
Medtronic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study aims at screening Israeli Arab men, smokers or past smokers, for abdominal aortic aneurysms (AAA). The screening is to be performed at the family doctors clinics in the rural arab erea of the north of Israel. Goals: The investigators aim at revealing the actual prevalence of AAA in the Israeli Arab smoking men population. By revealing this prevalence we believe the need for a nation-wide screening program for AAA will turn available for assessment. In addition, the goal of improving the accessibility of health services for the Israeli Arab population is a key issue in the design of the research. 2000 patients are to be enrolled in the study over a period of 2 years. Each of the patients will be examined once for a duplex ultra-sound and will be classified into one of 4 sub-groups according to the maximal aortic diameter found.
Detailed Description
Study Protocol No.:0017-14-COM Ultra-sound for AAA screening in smoking Israeli Arab men Initiator & Head researcher: Asaf Rabin, M.D. Vascular Clinic, Haifa and Western Galilee district, Clalit Health Services Horev Center, Haifa asafrabin@gmail.com +972-527-950-905 Signature: Contents Study Rationale & References --------------------------- 4-5 Goals ----------------------------------------------------------- 6 Research Design ---------------------------------------------- 7 Inclusion and exclusion criteria ----------------------------- 8 CRF---------------------------------------------------------- 9-10 End Points & Follow up chart -------------------------- 11-12 Confidentiality ------------------------------------------------ 13 Study Rationale In the United States ruptured abdominal aortic aneurysms (AAA) are the 15th leading cause of death overall and the 10th leading cause of death in men older than 55 years. The prevalence of AAA found in population-based ultrasonography (US) screening studies from various countries is about 4-9% in men and 1% in women older than 65yr. If left untreated, the aneurysm continues to expand; thinning of the aortic wall ensues and rupture may eventually occur. Most of large AAA are asymptomatic and often rupture occurs with no warning signs. Mortality due to rupture of an aortic aneurysm is high (80-90%), compared to 5-7% in elective surgery for AAA repair and even lower when treated by endovascular means (1-2%). Ultra-sound can reliably demonstrate the aorta in 99% of the population, and its sensitivity and specificity in diagnosing AAA approaches 95-100%. Screening with Ultra-sound for AAA has been proved in multiple studies to reduce AAA related mortality by an average of 42% in the screened population compared with the non-screened population. The reduction in mortality was achieved in a cost effective way. Based on such studies a number of screening programs have been implemented in the United Kingdom (UK), United States (USA), Scotland and Sweden. As for today there is no screening program for AAA in Israel. The investigators would like to conduct a study in a specific group of the population demonstrating the need for screening in such group. The major risk factors for AAA include Age (>65 years), male gender and a history of ever smoking. It has been demonstrated that smoking rates among Israeli Arab men are significantly higher than those of Israeli Jewish men. Most of the Israeli Arab population inhabits rural areas with less access to hospitals and medical centers. Therefore, the investigators decided to conduct a prospective study in which Israeli Arab men between the ages 60-80 years old, with a history of smoking, will undergo an ultra-sound examination for screening for AAA. Goals The investigators aim at revealing the actual prevalence of AAA in the Israeli Arab smoking men population. By revealing this prevalence the investigators believe the need for a nation-wide screening program for AAA will turn available for assessment. In addition, the goal of improving the accessibility of health services for the Israeli Arab population is a key issue in the design of the research. Performing the screening ultra-sound in the family-physician's clinics (see below under "Research Design") will save the patients the time and the trouble involved with being examined in the central vascular clinics. It will also improve the knowledge and awareness of the population in general and of the family-physicians in particular of the AAA disease and for the need of early diagnosis and treatment as mentioned above. Last but not least, the private benefit of each patient either from ruling out the option of having an AAA or from diagnosis of an AAA and referral to treatment is a valuable by-product of the research. Research Design 2000 men (according to the inclusion criteria) are planned to be included in the "screening study" over a period of one year to two years. The family-physicians of the Haifa and Western Galilee district, Clalit Health Services will be notified by the head researcher about the research. The organization will be asked to provide a list of potential patients according to the inclusion and exclusion criteria. The list will only include patients whom the physician had addressed and whom had given their approval for being approached by the research team. The patients will then be invited for a meeting with one of the researchers at the family-physician clinic. After a full explanation will be given, an informed consent form will be signed by the patient. Each patient will be documented on a Case Report Form (CRF) and will be given a code for the rest of the research. The coding system is aimed at securing the confidentiality of the patients' personal and medical information. Then after, with the help of the technician a Duplex Ultra-sound examination of the abdominal aorta will be performed. Since the examination is performed after a 6 hours fasting period, the fasting instruction will be given to the patients in advance. The results of the scans will be recorded in each patient Case Report Form (CRF). The patient will be classified according to the Duplex US findings into one of 4 sub-groups as detailed under "End-Points". A recommendation for further follow-up or treatment will be given to each patient and will be documented in his CRF accordingly. The results of the scan and the recommendations will be sent the patient and to his family-physician within a short period following the exam. It is to be made clear both hereby and in the informed consent form that the consent of the patient to participate in the research bares no further obligations to follow the recommendations of the research team nor to be followed-up or treated under the umbrella of the vascular service of Haifa and Western Galilee district, Clalit Health Services. Non-the-less, each of the patients is entitled for full follow-up and treatment by the vascular service of Haifa and Western Galilee district, Clalit Health Services regardless of his consent to participate in the research or to follow the research team recommendations. Each patient will be documented digitally in a separate research file. A copy of the informed consent will be given to patient. The same document will be scanned and filed in the patients research file. The file will also contain the CRF and the exam results. Study name: US for AAA screening in smoking Israeli Arab men Patient code: Date: Place: Case Report Form (CRF) Form filled at enrollment Age (60-80): Smoking: Active / in Past / No Y.P. - Israeli Arab man: Yes / No A known AAA Previous operations of the abdominal aorta Previous imaging study within the last 12 months, ruling-out AAA. Match to inclusion criteria: Yes / No --------------------------------------------------------------------------------- Weight: Height: Hypertension: Yes / No Diabetes mellitus: Yes / No Hypercholesterolemia/hyperlipidemia: Yes/ No Ischemic heart disease: Myocardial infarction- Yes/ No Coronary artery bypass- Yes/ No Catheterization - Yes/ No Origin of medical information: The patient - Yes / No The patient's relatives - Yes / No The patient's general physician - Yes / No Computerized medical file - Yes / No Other medical documents - Yes / No Ultra-sound results: Abdominal aorta maximal diameter- _____ cm Sub-group - A / B / C / D Date: ________ Physician name & signature:__________ End-Points & Follow up chart A formal report will be produced for every examination and will be signed by a vascular surgeon and sent to the patient and to his family-physician. The examined patient will be classified into one of the listed sub-groups according to the measured maximal aortic diameter. The head researcher will be responsible for inviting the patient for further follow-up or for additional work-up and treatment according to the findings. Result of screening US: Sub-group A: Normal Aorta (<3 cm) No need for follow up or extra imaging Sub-group B: Aortic Diameter ( 3-4.5 cm) Needs follow up: Annual aortic US Sub-group C: Aortic Diameter ( 4.5-5.5 cm) Needs follow up: Semiannual aortic US Sub-group D: Aortic Diameter (> 5.5cm) Further investigation and treatment: referral to Vascular Surgeon for treatment. Confidentiality The head researcher is committed for the confidentiality of the personal and medical information of the patient participating in the research. All the research documents will be coded and will contain no personal data. If personal details will be needed for the research they would be coded through a scrambling system for prevention of any identifying potential. The research data will be saved on a stand-alone computer and raw data will not be transferred or shared via internet. Clalit Health Services will be notified by the head-researcher for any occasion of data loss, theft or damage. The head-researcher will share the research raw data with any 3rd party only after a clear approval of Clalit Health Services is obtained. The research raw data will only be saved on a desk-top computer and not on any mobile electronic device.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdominal Aortic Aneurysm (AAA)
Keywords
Abdominal aortic aneurysm, Abdominal aortic aneurism, AAA, Screening, duplex ultra sound, Israeli Arab men, family physician

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
913 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Israeli Arab men
Arm Type
Other
Arm Description
Single arm study. The arm includes all enrolled patients screened by duplex ultra sound for abdominal aortic aneurysms.
Intervention Type
Other
Intervention Name(s)
Duplex ultra sound screening for abdominal aortic aneurysms
Intervention Description
Duplex ultra sound screening for abdominal aortic aneurysms in Israeli Arab men, smokers or past smokers at the age of 60-80 years.
Primary Outcome Measure Information:
Title
Abdominal aortic aneurysm prevalence in the represented population
Description
At the end of enrollment, estimated time - 2 years, the prevalence will be assessed.
Time Frame
2 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Arab men Age : 60-80 years old History of smoking Exclusion Criteria: A known AAA Previous operations of the abdominal aorta Previous imaging study within the last 12 months, ruling-out AAA.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Asaf Rabin, M.D.
Organizational Affiliation
Clalit Heath Services
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clalit Health Services primary clinics
City
Haifa
State/Province
Haifa and Western Galilee District & Northen District
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
15684209
Citation
Fleming C, Whitlock EP, Beil TL, Lederle FA. Screening for abdominal aortic aneurysm: a best-evidence systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 2005 Feb 1;142(3):203-11. doi: 10.7326/0003-4819-142-3-200502010-00012.
Results Reference
background
PubMed Identifier
23034729
Citation
Thompson SG, Ashton HA, Gao L, Buxton MJ, Scott RA; Multicentre Aneurysm Screening Study (MASS) Group. Final follow-up of the Multicentre Aneurysm Screening Study (MASS) randomized trial of abdominal aortic aneurysm screening. Br J Surg. 2012 Dec;99(12):1649-56. doi: 10.1002/bjs.8897. Epub 2012 Oct 3.
Results Reference
background
PubMed Identifier
15684208
Citation
U.S. Preventive Services Task Force. Screening for abdominal aortic aneurysm: recommendation statement. Ann Intern Med. 2005 Feb 1;142(3):198-202. doi: 10.7326/0003-4819-142-3-200502010-00011. No abstract available.
Results Reference
background
PubMed Identifier
15545293
Citation
Norman PE, Jamrozik K, Lawrence-Brown MM, Le MT, Spencer CA, Tuohy RJ, Parsons RW, Dickinson JA. Population based randomised controlled trial on impact of screening on mortality from abdominal aortic aneurysm. BMJ. 2004 Nov 27;329(7477):1259. doi: 10.1136/bmj.38272.478438.55. Epub 2004 Nov 15. Erratum In: BMJ. 2005 Mar 12;330(7491):596.
Results Reference
background
PubMed Identifier
12844092
Citation
Wilmink AB, Quick CR, Hubbard CS, Day NE. Effectiveness and cost of screening for abdominal aortic aneurysm: results of a population screening program. J Vasc Surg. 2003 Jul;38(1):72-7. doi: 10.1016/s0741-5214(03)00135-6.
Results Reference
background
PubMed Identifier
12081734
Citation
Vardulaki KA, Walker NM, Couto E, Day NE, Thompson SG, Ashton HA, Scott RA. Late results concerning feasibility and compliance from a randomized trial of ultrasonographic screening for abdominal aortic aneurysm. Br J Surg. 2002 Jul;89(7):861-4. doi: 10.1046/j.1365-2168.2002.02133.x.
Results Reference
background
PubMed Identifier
12443589
Citation
Ashton HA, Buxton MJ, Day NE, Kim LG, Marteau TM, Scott RA, Thompson SG, Walker NM; Multicentre Aneurysm Screening Study Group. The Multicentre Aneurysm Screening Study (MASS) into the effect of abdominal aortic aneurysm screening on mortality in men: a randomised controlled trial. Lancet. 2002 Nov 16;360(9345):1531-9. doi: 10.1016/s0140-6736(02)11522-4.
Results Reference
background
PubMed Identifier
17331750
Citation
Lindholt JS, Juul S, Henneberg EW. High-risk and low-risk screening for abdominal aortic aneurysm both reduce aneurysm-related mortality. A stratified analysis from a single-centre randomised screening trial. Eur J Vasc Endovasc Surg. 2007 Jul;34(1):53-8. doi: 10.1016/j.ejvs.2006.12.031. Epub 2007 Feb 28.
Results Reference
background
PubMed Identifier
23523277
Citation
Davis M, Harris M, Earnshaw JJ. Implementation of the National Health Service Abdominal Aortic Aneurysm Screening Program in England. J Vasc Surg. 2013 May;57(5):1440-5. doi: 10.1016/j.jvs.2012.10.114. Epub 2013 Mar 21.
Results Reference
background
PubMed Identifier
21348400
Citation
Baron-Epel O, Keinan-Boker L, Weinstein R, Shohat T. Persistent high rates of smoking among Israeli Arab males with concomitant decrease among Jews. Isr Med Assoc J. 2010 Dec;12(12):732-7.
Results Reference
background

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Ultra-sound for AAA Screening in Smoking Israeli Arab Men

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