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Whipple Procedure: Standard of Care vs. Thunderbeat

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The Washington University

Status

Terminated

Conditions

Bile Duct Carcinoma
Pancreatic Neoplasms

Treatments

Device: Thunderbeat
Device: Standard of care scissors, ligatures, clips, and sutures

Study type

Interventional

Funder types

Other

Identifiers

NCT02204124
201311146

Details and patient eligibility

About

The Whipple procedure is the standard method for therapy for cancerous tumors, inflammation, and stenosis (narrowing) near the head of the pancreas. This is a prospective study to assess whether or not use of the Thunderbeat™ device may decrease blood loss and postoperative morbidity (the presence of illness or disease). The findings will then be compared to patients whose Whipple procedure will be performed using conventional dissection and hemostasis techniques.

Full description

As the pancreas is fed by many vessels, it is necessary to use lots of ligatures, clips and sutures for hemostasis after dissection. This dissection technique is very time consuming and requires numerous changes of instruments. The devices the investigators currently have available for use in the operating suite are EnSeal and LigaSure. A new type of surgical scissors that delivers ultrasonically generated frictional heat energy and electrically generated bipolar energy simultaneously, known as the Thunderbeat™ (Olympus, Japan), is now an available alternative for dissection and hemostasis.

Thunderbeat™ was provided FDA clearance in March 2012 for use in open, laparoscopic, and endoscopic surgery, or in any procedure in which cutting, vessel ligation (sealing and cutting), coagulation, grasping and dissection is performed.

The Thunderbeat™ device provides the first integration of both bipolar and ultrasonic energies delivered simultaneously from a single multi-functional instrument. This integration provides the surgeon the ability to rapidly cut tissue with ultrasonic energy and to create reliable vessel seals with bipolar energy without having to change devices. The current is provided by a special generator and contains a very high capacity with a low voltage. The body's proteins, such as collagen and elastin, are converted so a permanently sealed zone results. As the tissue between the branches is sealed, lateral thermic tissue damages can be limited to a minimum. Several authors have described a tendency of reduced intraoperative blood loss with bipolar energy devices. Other trials show reduced operating time when a bipolar device is utilized in several surgical procedures, such as thyroid, hepatic, urologic, hemorrhoidectomy and gynecology surgery.

Correct dissection in the operating field is very important to avert secondary bleeding or other complications, which might cause re-operation or elevate the patients' morbidity and mortality.

Enrollment

44 patients

Sex

All

Ages

22 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Scheduled to undergo an elective open or laparoscopic Whipple procedure
  • At least 22 years of age.
  • Karnofsky performance status greater than or equal to 80%.
  • Able to understand and willing to sign a written informed consent document.

Exclusion criteria

  • Pregnant or breastfeeding.
  • Surgeon's opinion at the time of dissection that the subject's well being (e.g. bleeding or other independent acute health problems) would be compromised.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

44 participants in 2 patient groups

Control Group
Active Comparator group
Description:
In the control group, scissors, ligatures, clips and sutures will be used for dissection and hemostasis as necessary.
Treatment:
Device: Standard of care scissors, ligatures, clips, and sutures
Thunderbeat™
Experimental group
Description:
-In the Thunderbeat™ group, dissection and hemostasis of vessels will be performed using the Thunderbeat™ device (Olympus, Japan).
Treatment:
Device: Thunderbeat

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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