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Ultrasonically Activated Scalpel Versus Electrocautery Based Dissection in Acute Cholecystitis Trial

Primary Purpose

Cholecystitis, Acute

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Ultrasonically activated scalpel
Electrocautery
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cholecystitis, Acute

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Emergency laparoscopic cholecystectomy performed for cholecystitis
  • American Society of Anesthesiologists (ASA) score I-III

Exclusion Criteria:

  • Patients unable to express themselves in Swedish
  • Pregnancy
  • Previous open surgery in the upper abdomen
  • American Society of Anesthesiologists (ASA) score >III

Sites / Locations

  • Karolinska University Hospital, Center for Digestive DiseasesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Ultrasonically activated scalpel

Electrocautery

Arm Description

Dissection with ultrasonically activated scalpel. Direction of dissection undecided but by experience most naturally fundus first.

Dissection with electrocautery. Direction of dissection undecided but by experience most naturally cystic duct first.

Outcomes

Primary Outcome Measures

Postoperative complications
Postoperative complications registered according to Clavien-Dindo

Secondary Outcome Measures

Operative time
Time required to complete surgery
Level of technical complexity
Level of technical complexity of the procedure as assessed by the surgeon
Technical performance
Perioperative technical performance assessed by an independent observer
Postoperative stay
Time from surgery to duscharge
Sick leave
Time from surgery to return to work
Conversion rate
Conversion from laparoscopic to open cholecystyectomy
Postoperative pain
Daily assessments of pain on a visual analogue scale
Postoperative inflammatory activity
Daily measurements of c-reactive protein and leukocyte particle concentration
Conversion rate
Number of procedures converted to open cholecystectomy
Direct and indirect medical costs
Analysis of health economics

Full Information

First Posted
January 5, 2017
Last Updated
March 1, 2023
Sponsor
Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT03014817
Brief Title
Ultrasonically Activated Scalpel Versus Electrocautery Based Dissection in Acute Cholecystitis Trial
Official Title
Ultrasonically Activated Scalpel Versus Electrocautery Based Dissection in Acute Cholecystitis. A Randomized, Double Blind, Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2019 (Actual)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The present study aims at analyzing whether ultrasonic tissue coagulation dissection technique offers a smoother peri- and postoperative course and reduces the risk for conversion from laparoscopic to open surgery in acute cholecystectomy patients as compared to electrocautery in case of acute cholecystitis The study is performed as a double-blinded study on patients undergoing laparoscopic surgery for acute cholecystitis. Patients included in the study are randomized to surgery with either the traditional electrocautery based technique or ultrasonic scalpel based dissection.
Detailed Description
Electrocautery is traditionally the method of choice for tissue dissection in laparoscopic cholecystectomy. As an alternative to electrocautery, the ultrasonically activated scalpel has proven to be an effective and safe instrument for the facilitation of dissection and to minimize blood loss in both open and laparoscopic surgery. Whereas electrocautery coagulates by burning at temperatures higher than 150ºC, the ultrasonic scalpel transforms the electric power into mechanical longitudinal vibration of the working part of the instrument by a piezoelectrical transducer. Accordingly, the former technique limits the heating- thermal necrosis effect on the tissue to the area just adjacent to the cutting line. Since the relative-potential benefit of the ultrasonic scalpel is high in technically demanding surgery, the advantage may not be as pronounced in routine laparoscopic gallstone surgery, which can usually be done more uneventfully whichever equipment is used. Laparoscopic cholecystectomy for acute cholecystitis is, however, more demanding connected with longer operative time, more postoperative complications, greater risk of conversion to open cholecystectomy and longer postoperative stay. In addition, we know that operations for acute cholecystitis are associated with a higher risk for severe complications such as bile duct injury. The potential benefit from using the ultrasonic scalpel is thus even greater when doing surgery for cholecystitis. In addition to this there are numerous important aspects on the safety in the implementation of the emergency cholecystectomy. Traditionally, most surgeons have chosen to operate these patients with laparoscopic technique, with the use of a so-called electrocautery hook, which usually allows tissue division with minimal blood loss. Further improvements in the dissection technique followed the introduction of ultrasonic tissue coagulation. This technique offers the option of performing these operations with even less blood loss, a more gentle handling of the inflamed tissue and a sealing of the tissue sections while the tissue is divided. Accordingly this ultrasonic tissue coagulation technique can theoretically be of significant advantage not the least when dividing acutely inflamed tissue like in acute cholecystitis with particular relevance for the dissection of the gallbladder from the liver bed, where bleeding and bile leakage often occurs. Moreover if the surgeon instead chooses to dissect the gallbladder from the doom and downwards, to the part that contains the cystic duct and cystic artery (Calots triangle), unique options can be offered to not only simplify the operation but also make it safer. This latter technique is called "fundus first". The present study aims at analyzing whether ultrasonic tissue coagulation dissection technique combined with "fundus first" approach offers a smoother per and postoperative course in acute cholecystectomy patients as compared to the traditional way of performing the operation. Due to the lower risk of bleeding and better anatomical overview, the technique may also reduce the risk of having to convert the procedure for laparoscopic cholecystectomy to open cholecystectomy. The study is performed as a double-blinded study on patients undergoing laparoscopic surgery for acute cholecystitis. Patients included in the study are randomized to surgery with either the traditional electrocautery based technique or ultrasonic scalpel based dissection with the "fundus first" approach. The choice of dissection approach is determined by the randomization procedure, whether it is done from the triangle of Callot + electrocautery and upwards or from the gallbladder fundus and downwards by the use of the ultrasonic scalpel. Peroperative cholangiography is done routinely. The cystic duct is closed with a clip, not with the ultrasonic scalpel. One month after surgery the patient is contacted by a telephone. In cases the questionnaires have not been returned yet, the patient is reminded about this. At the phone call the exact number of days of sick leave postoperatively and any adverse events occurring after discharge are recorded.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholecystitis, Acute

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ultrasonically activated scalpel
Arm Type
Experimental
Arm Description
Dissection with ultrasonically activated scalpel. Direction of dissection undecided but by experience most naturally fundus first.
Arm Title
Electrocautery
Arm Type
Active Comparator
Arm Description
Dissection with electrocautery. Direction of dissection undecided but by experience most naturally cystic duct first.
Intervention Type
Procedure
Intervention Name(s)
Ultrasonically activated scalpel
Intervention Description
Dissection with ultrasonically activated scalpel
Intervention Type
Procedure
Intervention Name(s)
Electrocautery
Intervention Description
Dissection with electrocautery
Primary Outcome Measure Information:
Title
Postoperative complications
Description
Postoperative complications registered according to Clavien-Dindo
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Operative time
Description
Time required to complete surgery
Time Frame
3 hours
Title
Level of technical complexity
Description
Level of technical complexity of the procedure as assessed by the surgeon
Time Frame
3 hours
Title
Technical performance
Description
Perioperative technical performance assessed by an independent observer
Time Frame
3 hours
Title
Postoperative stay
Description
Time from surgery to duscharge
Time Frame
14 days
Title
Sick leave
Description
Time from surgery to return to work
Time Frame
30 days
Title
Conversion rate
Description
Conversion from laparoscopic to open cholecystyectomy
Time Frame
3 hours
Title
Postoperative pain
Description
Daily assessments of pain on a visual analogue scale
Time Frame
7 days
Title
Postoperative inflammatory activity
Description
Daily measurements of c-reactive protein and leukocyte particle concentration
Time Frame
7 days
Title
Conversion rate
Description
Number of procedures converted to open cholecystectomy
Time Frame
3 hours
Title
Direct and indirect medical costs
Description
Analysis of health economics
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Emergency laparoscopic cholecystectomy performed for cholecystitis American Society of Anesthesiologists (ASA) score I-III Exclusion Criteria: Patients unable to express themselves in Swedish Pregnancy Previous open surgery in the upper abdomen American Society of Anesthesiologists (ASA) score >III
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
My Blohm, MD
Phone
+46702900521
Email
My.Blohm@ltdalarna.se
First Name & Middle Initial & Last Name or Official Title & Degree
Gabriel Sandblom, Assoc Prof
Phone
+46 70 415 82 18
Email
gabriel.sandblom@ki.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gabriel Sandblom, Assoc Prof
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska University Hospital, Center for Digestive Diseases
City
Stockholm
ZIP/Postal Code
14186
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriel Sandblom, Ass Prof
Phone
+46704158218
Email
gabriel.sandblom@ki.se

12. IPD Sharing Statement

Plan to Share IPD
No

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Ultrasonically Activated Scalpel Versus Electrocautery Based Dissection in Acute Cholecystitis Trial

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