Random Comparison of LigaSure and Disposable Staples for Laparoscopic Surgery

NCT ID: NCT00487409

Last Updated: 2014-12-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-12-31

Study Completion Date

2010-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this research is to compare two different standard of care surgical methods for the following large bowel (colon) procedures: laparoscopic right colectomy, total colectomy, and left colectomy. The study will compare electrocautery, used with surgical clips and/or surgical staplers, and the Ligasure vessel sealer. The investigators will be looking at which procedure is faster and more cost efficient and the investigators will calculate hospital expenses for the two groups to make comparisons.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The application of laparoscopic surgery has expanded over the last decade to include many complex abdominal procedures that have traditionally been performed through a laparotomic incision. The widespread acceptance and utilization of laparoscopy has directly resulted in a continuing need to develop both new techniques and ancillary surgical instrumentation.

Laparoscopic instruments that provide adequate hemostasis and allow for precise dissection of tissues are needed for a safe and efficient operation. Furthermore, as new devices emerge and the volume of laparoscopic cases increases the importance of cost and ergonomically sound instrumentation have become apparent.

The safety and efficacy of laparoscopic colectomy for benign disease has been demonstrated by several case series over the last decade. The advantages of smaller wounds, shorter ileus, earlier resumption of dietary intake, and reductions in hospital stay have been consistently reported as the major benefits of this approach. More recently, in a multi-center randomized prospective trial laparoscopic colectomy for curable cancer resulted in equivalent cancer related survival to open colectomy when performed by experienced surgeons. Adherence to standard cancer resection techniques including but not limited to complete exploration of the abdomen, adequate proximal and distal margins, ligation of the major vessels at their respective origins, containment and careful tissue handling, and en bloc resection with negative tumor margins using the laparoscopic approach resulted in acceptable outcomes.

The advantages of standardized surgical technique's for laparoscopic colectomy that were discussed in this multicenter trial were well outlined in one previous study. This study retrospectively reviewed a consecutive series of patients undergoing laparoscopic sigmoid colectomy from 1999 to 2001 at a single institution. The potential benefits of a standardized technique included 1) standardization of surgical instrument sets, 2) definition of benchmarks for the decision to convert before inappropriate investments in time and equipment, and 3) provision of an easily transferred skill set for residents in training.

Despite the obvious value of this standardized approach, a variety of techniques and laparoscopic instruments for tissue dissection and coagulation are currently utilized. These options include laparoscopic staplers, lap clip appliers, suture ligature, electrothermal bipolar vessel sealers, electric cautery, and ultrasonic shears. Dissection, coagulation, and the division of the mesocolon and mesorectum during laparoscopy, continue to represent a technical and hemostatic challenge. When dealing with inflamed tissues, as in diverticulitis or inflammatory bowel disease, or when the mesocolon and mesorectum are fatty, reliable hemostasis is not always easy to obtain. Concerning tissue dissection and coagulation, electrosurgery, widely implemented in open surgery, has displayed some complications and limits related to minimally invasive techniques. The search for safer multidimensional instruments has led to the development of both the ultrasonic dissector(UCS), (Harmonic Scalpel, Ultracision, Ethicon Endosurgery Inc., Cincinnati, OH) and the endoscopic Ligasure (LIG or EBVS), (Valleylab, Boulder, CO).

Use of ultrasonic dissection in colorectal laparoscopic surgery has recently been reviewed retrospectively in two studies. Both studies concluded that ultrasonic dissection was safe and effective. A prospective randomized clinical trial also demonstrated that use of UCS provided the advantage of a decreased blood loss when compared with ES without and any increase in morbidity.

Recently an electrothermal bipolar vessel sealer, (EBVS) (Ligasure, Valleylab, Boulder, CO, USA) was developed for both laparoscopic and open procedures as an alternative to suture ligatures, hemoclips, staplers and ultrasonic coagulator's for ligating vessels, and tissue bundles. The EBVS is approved by the Food and Drug Administration to seal vessels up to 7mm in diameter. It does so by applying high current and low voltage, which differs from the energy used in standard monopolar and bipolar cautery. This unique form of energy denatures collagen and elastin within the vessel wall and surrounding connective tissue. The addition of extreme pressure applied by the instrument, which also differs from other energy sources, causes the denatured protein to reform, with the vessel walls in apposition. Clinically, the result is a nearly translucent "seal" that may be transected. The Ligasure device has been used in all types of gastrointestinal surgery including small and large bowel resection, gastrectomy, pancreatectomy, splenectomy, esophagogastric devascularization for portal hypertension, and transplantation. To date, the device appears to be cost effective in teaching institutions when used in difficult open and laparoscopic surgery.

The initial results with the EBVS and colorectal surgery were from a prospective review of 98 cases by a single surgeon from 1998 to 2000. These included both laparoscopic and open cases and involved 53 colon resections. No postoperative hemorrhagic complication occurred and there was an estimated mean reduction in operative time of 39 minutes. Additionally, the same authors' applied the ligasure technology to a pig animal model and consistently reported no evidence of postoperative bleeding. They concluded that the EBVS was safe and effective and may potentially reduce operative times.

A second study, also a retrospective analysis, compared Ligasure to an ultrasonic coagulator for total abdominal colectomy in 15 patients with ulcerative colitis. The procedure using Ligasure reduced the operating time, intraoperative bleeding and operator's stress in comparison with ultrasonic coagulation.

A third study, another retrospective comparative model, was conducted to address the differences between EBVS and ultrasonic shears for laparoscopic transverse and sigmoid colectomy. The study included 30 patients and found that the incidence of rebleeding was significantly lower in the EBVS group than in the the UCS group for both surgical procedures. In addition the required time for mesocolon dissection was also significantly shorter when the EBVS was used.

The only prospective randomized study with Ligasure and laparoscopic colorectal surgery addressed the speed, reliability and cost to guide surgeons in their choice for intracorporeal pedicle ligation. This study involved both straight laparoscopy and hand-assisted laparoscopy and compared laparoscopic vascular staplers and disposable clip appliers with the Ligasure Atlas during elective right, left, and total colectomy. Cases were stratified by procedure and failure was defined as any bleeding after pedicle ligation. 100 patients were included in the study and the Ligasure atlas was found to be more cost effective and associated with lower failure rates.

Significance and Purpose The utilization and safety of surgical staplers and disposable clips for laparoscopic colectomy is established and has been adopted by the majority of surgeon's performing these procedures. Although the growing evidence supporting the application of Ligasure to laparoscopic colorectal surgery has demonstrated its safety and efficiency, most of the studies have been limited by sample size and their retrospective nature. There also have been several questions left unanswered. A standardized approach for laparoscopic right, total, and left colectomy has never been substantiated by any prospective study. Furthermore, the difficult and somewhat dangerous steps involved with division of the mesorectum during both laparoscopic sigmoid colectomy and low anterior resection have not been appropriately evaluated.

The objective of this study is to determine the best technical approach to laparoscopic right, total, and left colectomy by comparing the utilization of the Ligasure device to electrocautery with the application of surgical clips and/or surgical stapler's. To answer this question the investigators will compare each approach regarding tissue dissection, colonic mobilization and pedicle ligation. Safety, cost, operative time, time to pedicle ligation and hemostasis will be objectively measured in each treatment group.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Colonic Diseases Rectal Diseases

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Ulcerative colitis Crohn's disease Colorectal polyps Colorectal malignancy Endometriosis Diverticulitis Colonic inertia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group A

Standard of Care

Group Type OTHER

Disposable stapling instruments

Intervention Type PROCEDURE

laparoscopic colectomy using clips, cautery and stapler

Group B

Standard of Care

Group Type OTHER

Bipolar electrosurgical generator and instruments

Intervention Type PROCEDURE

laparoscopic colectomy using the Ligasure device

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Bipolar electrosurgical generator and instruments

laparoscopic colectomy using the Ligasure device

Intervention Type PROCEDURE

Disposable stapling instruments

laparoscopic colectomy using clips, cautery and stapler

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Ligasure Device Staples or Clips

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Subjects who have benign or malignant colonic or rectal disease that mandate resection and are approached laparoscopically. Potential indications or conditions include ulcerative colitis, Crohn's disease, colorectal polyps, colorectal malignancy, endometriosis, diverticulitis, and colonic inertia
* Subjects who are 18 years of age and older
* Subjects of either sex
* Subjects who are willing and able to adhere to protocol requirements, agree to participate in the study program and provide written and informed consent

Exclusion Criteria

* Subjects who undergo conversion to the open approach before mobilization of the colon or pedicle ligation will be excluded from the analysis
* Subjects who are pregnant
* Subjects who have undergone a previous colectomy
* Subjects with a medical condition that may interfere with the evaluation of safety or effectiveness of the study device
* Subjects who have another condition that in the opinion of the investigator precludes further participation in the study
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Tyco Healthcare Group

INDUSTRY

Sponsor Role collaborator

University Hospitals Cleveland Medical Center

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Conor Delaney, MD, PhD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Conor P. Delaney, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospitals of Cleveland/ Institute for Surgical Innovation

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University Hospitals of Cleveland Case Medical Center

Cleveland, Ohio, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

Explore related publications, articles, or registry entries linked to this study.

Adamina M, Champagne BJ, Hoffman L, Ermlich MB, Delaney CP. Randomized clinical trial comparing the cost and effectiveness of bipolar vessel sealers versus clips and vascular staplers for laparoscopic colorectal resection. Br J Surg. 2011 Dec;98(12):1703-12. doi: 10.1002/bjs.7679. Epub 2011 Oct 13.

Reference Type DERIVED
PMID: 21997317 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

10-06-33

Identifier Type: -

Identifier Source: org_study_id