search
Back to results

Whipple Procedure: Standard of Care vs. Thunderbeat

Primary Purpose

Pancreatic Neoplasms, Bile Duct Carcinoma

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Thunderbeat
Standard of care scissors, ligatures, clips, and sutures
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Neoplasms focused on measuring Whipple procedure

Eligibility Criteria

22 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept 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.

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control Group

Thunderbeat™

Arm Description

In the control group, scissors, ligatures, clips and sutures will be used for dissection and hemostasis as necessary.

-In the Thunderbeat™ group, dissection and hemostasis of vessels will be performed using the Thunderbeat™ device (Olympus, Japan).

Outcomes

Primary Outcome Measures

Operative Blood Loss
The measurement of estimated blood loss (EBL) will come from the intraoperative anesthesia notes where (EBL) is recorded during each surgical procedure The estimate of operative blood loss is measured by volume in the suction canisters and pads and is historically documented by the operative nursing staff during the operation.
Post-op Morbidity
-This is a prospective study to evaluate post-operative morbidity following use of the ThunderbeatTM device during the Whipple procedure. This will be compared to patients whose Whipple procedure will be performed using conventional dissection and hemostasis techniques.

Secondary Outcome Measures

Operative Time
-Operation time measured from the beginning of the surgical procedure (incision of the skin) to the end of the surgical procedure (closure of the skin).
Cost Using Thunderbeat Device
-Calculated by the indirect and direct costs during the hospital stay and the costs accumulated 90 days postoperatively
Anesthesia Time
-Anesthesia time measured from the initiation of anesthesia induction to the time of extubation
Number of Participants Who Experienced Perioperative Complications
-Complications experienced during surgery will be reviewed including: Iatrogenic injury need for conversion from laparoscopic approach to open procedure need for the use of other hemostatic devices or therapies intraoperative requirement of blood product transfusion
Number of Participants Who Experienced Postoperative Complications
-Complications experienced after surgery will be reviewed including: secondary bleeding/hematoma wound infection gastroparesis postoperative pancreatic fistula intraabdominal abscess anastomotic leakage re-intervention (operational) postop requirement for blood product transfusion hospital mortality

Full Information

First Posted
July 23, 2014
Last Updated
August 22, 2018
Sponsor
Washington University School of Medicine
search

1. Study Identification

Unique Protocol Identification Number
NCT02204124
Brief Title
Whipple Procedure: Standard of Care vs. Thunderbeat
Official Title
Thunderbeat™ Integrated Bipolar and Ultrasonic Forceps in the Whipple Procedure: A Prospective Registry Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Terminated
Why Stopped
Principal Investigator and Study Sponsor decided to terminate the study early
Study Start Date
January 1, 2015 (Actual)
Primary Completion Date
August 23, 2017 (Actual)
Study Completion Date
August 23, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Neoplasms, Bile Duct Carcinoma
Keywords
Whipple procedure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
The participants will be blinded to the assigned operating technique.
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
In the control group, scissors, ligatures, clips and sutures will be used for dissection and hemostasis as necessary.
Arm Title
Thunderbeat™
Arm Type
Experimental
Arm Description
-In the Thunderbeat™ group, dissection and hemostasis of vessels will be performed using the Thunderbeat™ device (Olympus, Japan).
Intervention Type
Device
Intervention Name(s)
Thunderbeat
Intervention Description
Thunderbeat uses ultrasonic and high frequency bipolar energy simultaneously to seal and cut tissue compared to placebo comparator.
Intervention Type
Device
Intervention Name(s)
Standard of care scissors, ligatures, clips, and sutures
Primary Outcome Measure Information:
Title
Operative Blood Loss
Description
The measurement of estimated blood loss (EBL) will come from the intraoperative anesthesia notes where (EBL) is recorded during each surgical procedure The estimate of operative blood loss is measured by volume in the suction canisters and pads and is historically documented by the operative nursing staff during the operation.
Time Frame
Day of surgery
Title
Post-op Morbidity
Description
-This is a prospective study to evaluate post-operative morbidity following use of the ThunderbeatTM device during the Whipple procedure. This will be compared to patients whose Whipple procedure will be performed using conventional dissection and hemostasis techniques.
Time Frame
Up to 90 days postoperatively
Secondary Outcome Measure Information:
Title
Operative Time
Description
-Operation time measured from the beginning of the surgical procedure (incision of the skin) to the end of the surgical procedure (closure of the skin).
Time Frame
Day of surgery
Title
Cost Using Thunderbeat Device
Description
-Calculated by the indirect and direct costs during the hospital stay and the costs accumulated 90 days postoperatively
Time Frame
Up to 90 days postoperatively
Title
Anesthesia Time
Description
-Anesthesia time measured from the initiation of anesthesia induction to the time of extubation
Time Frame
Day of surgery
Title
Number of Participants Who Experienced Perioperative Complications
Description
-Complications experienced during surgery will be reviewed including: Iatrogenic injury need for conversion from laparoscopic approach to open procedure need for the use of other hemostatic devices or therapies intraoperative requirement of blood product transfusion
Time Frame
Day of surgery
Title
Number of Participants Who Experienced Postoperative Complications
Description
-Complications experienced after surgery will be reviewed including: secondary bleeding/hematoma wound infection gastroparesis postoperative pancreatic fistula intraabdominal abscess anastomotic leakage re-intervention (operational) postop requirement for blood product transfusion hospital mortality
Time Frame
Up to 90 days postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
22 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William Hawkins, M.D.
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.siteman.wustl.edu
Description
Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine

Learn more about this trial

Whipple Procedure: Standard of Care vs. Thunderbeat

We'll reach out to this number within 24 hrs