LapAorta: Laparoscopic Versus Open Abdominal Aortic Aneurysm (AAA) Exclusion

Sponsor
Augusta Hospital Duesseldorf (Other)
Overall Status
Withdrawn
CT.gov ID
NCT00821145
Collaborator
Storz GmbH FRG (Other), Tel Aviv University (Other)
0
3
17

Study Details

Study Description

Brief Summary

In many countries the gold standard for treating abdominal aortic aneurysms is still open surgery with a long incision. In patients with suitable anatomy alternatively an endovascular approach can be chosen. Since open surgery is more durable in many countries a laparoscopic procedure using " key hole surgery " has gained wider acceptance. The current study wants to prove that laparoscopic aortic aneurysm procedures are less invasive than open surgery with reduced recovery times.

Condition or Disease Intervention/Treatment Phase
  • Procedure: conventional surgery
  • Procedure: laparoscopic AAA resection
  • Procedure: laparoscopic stapler anastomosis
Phase 3

Detailed Description

In many countries the gold standard for treating abdominal aortic aneurysms is still open surgery with a long incision. In patients with suitable anatomy alternatively an endovascular approach can be chosen. Since open surgery is more durable in many countries a laparoscopic procedure using " key hole surgery " has gained wider acceptance. The current study wants to prove that laparoscopic aortic aneurysm procedures are less invasive than open surgery with reduced recovery times.

Study design: Multi center prospective randomized study including patients with infra or juxtarenal aortic aneurysms ( AAA).

In group I the AAA is resected using a conventional long incision and standard procedures for resecting the AAA. A Dacron graft is used in inlay technique to restore blood flow.

In group II a total laparoscopic approach is chosen to exclude the AAA. Identical to open surgery a dacron graft is laparoscopically sawn in to exclude the AAA and to restore blood flow.

In a subgroup II a the laparoscopic anastomosis is performed with a stapling device to simplify and to accelerate the procedure.

Endpoints of the study:

Total operating time, aortic crossclamping time, stay in ICU, return to a regular diet,postoperative ileus, total hospital stay, major and minor complications, blood loss, renal function in cases with juxtarenal AAA.Patients are evaluated for postoperative pain, wound related problems, hernias and time until full mobilisation is achieved.

Hypothesis: The laparoscopic approach though associated with a longer operating time and longer clamping times is associated with a reduced recovery time, les pain and less wound related problems compared to a full length conventional incision.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Laparoscopic Aortic Resection Versus Open Surgery in Patients With AAA
Study Start Date :
Jan 1, 2009
Anticipated Primary Completion Date :
Jun 1, 2010
Anticipated Study Completion Date :
Jun 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 1

50 patients operated using a conventional open surgery to exclude an abdominal aortic aneurysm

Procedure: conventional surgery
AAA patients operated using a conventional incision

Experimental: 2

50 patients operated using a total laparoscopic aortic aneurysm resection

Procedure: laparoscopic AAA resection
laparoscopic AAA resection

Active Comparator: 3

25 patients using a laparoscopic approach for AAA resection with a stapled proximal anastomosis

Procedure: laparoscopic stapler anastomosis
laparoscopic AAA resection, proximal anastomosis performed with a stapler

Outcome Measures

Primary Outcome Measures

  1. All cause mortality, reduced recovery postoperatively according to pain measurement, ICU and hospital stay, minor and major complications [1 year]

Secondary Outcome Measures

  1. Use of a stapling device reduces total operative time and crossclamping period [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients with abdominal aortic aneurysms

  • fit for open surgery

Exclusion Criteria:
  • patients unfit for open surgery

  • patients with malignancies

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Augusta Hospital Duesseldorf
  • Storz GmbH FRG
  • Tel Aviv University

Investigators

  • Principal Investigator: Ralf R Kolvenbach, M.D.PhD, Augusta Hospital Duesseldorf

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00821145
Other Study ID Numbers:
  • LapAorta2008
First Posted:
Jan 13, 2009
Last Update Posted:
Jul 12, 2012
Last Verified:
Jan 1, 2009
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 12, 2012