Optimum-pressure for Reducing Postoperative Shoulder-tip Pain in Laparoscopic Cholecystectomy
Primary Purpose
Pain, Postoperative
Status
Unknown status
Phase
Not Applicable
Locations
Thailand
Study Type
Interventional
Intervention
Intraabdominal pressure
Sponsored by
About this trial
This is an interventional treatment trial for Pain, Postoperative
Eligibility Criteria
Inclusion Criteria:
- Age > 15 years
- Elective procedure of laparoscopic cholecystectomy
- Sign to Inform consent
Exclusion Criteria:
- Emergency surgery
- Concomitant other procedure performed
- Deny to participant
Sites / Locations
- Faculty of Medicine, Ramathibodi Hospital, Mahidol UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control group
Study group
Arm Description
8 mmHg pressure group
10 mmHg group
Outcomes
Primary Outcome Measures
Shoulder tip pain
The shoulder tip pain was assessed by the investigator during postoperative period unfil 48 hours. The measurement of the outcome, the investigator would ask the participant by the clinical record form and questionnair. The answer of the questionnaire is presence or absence of the shoulder pain or pain around the shoulder and scapular region.
Secondary Outcome Measures
Change of intra-abdominal pressure
The change of intra-abminal pressure was measure by two parameters. Firstly, the adjustment of the pressure during the operation was recorded by the questionnaire. The answer of the questionnaire is the presence or absence of the intra-abdominal pressure change. Secondly, the maximum intra-abdominal pressure which is the highest pressure used during the operation, is measure by the level of the pressure appearing in the laparoscopic station by mmHg unit.
Difficulty of the operation
The difficulty level of the operation which evaluated by the surgeons. The measurement of this outcome by the questionnaire.
Full Information
NCT ID
NCT04212936
First Posted
December 23, 2019
Last Updated
February 23, 2021
Sponsor
Mahidol University
1. Study Identification
Unique Protocol Identification Number
NCT04212936
Brief Title
Optimum-pressure for Reducing Postoperative Shoulder-tip Pain in Laparoscopic Cholecystectomy
Official Title
Optimum-pressure for Reducing Postoperative Shoulder-tip Pain in Laparoscopic Cholecystectomy, a Prospective Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 25, 2019 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
June 30, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mahidol University
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
Laparoscopic cholecystectomy (LC) is the standard treatment of gallbladder disease. LC is the common procedure for general surgeons. Although LC is a safe procedure with very low mortality (<1%), it has some associated major morbidity. Bile duct injury is the most serious complication of LC. However, there are some postoperative morbidity including shoulder-tip pain. The incidence of shoulder-tip pain is about 15-45%, which might be influencing the patient outcome including length of hospital stay. From the previous studies, one of the important factor associated with this condition is pneumoperitoneum pressure. Thus, the suggestion of the intra-abdominal pressure should be low pressure as about 8 mmHg. However, the optimum pressure for the low-pressure during laparoscopic cholecystectomy is controversial.
Detailed Description
We designed the prospective randomized controlled trial to comparing the postoperative shoulder tip pain between two low pressure level (8 and 10 mmHg) during laparoscopic cholecystectomy. After the enrolled participant signed the inform consent, the participant was randomly assigned to 8 or 10 mmHg group. The standard procedure of the laparoscopic cholecystectomy was performed by experience surgeons. During the operation, the pressure limit can be adjusted to facilitate the procedure according to the surgeons. Following the operation, the investigator will ask about the shoulder tip pain from the participant during 48 hours. The standard of care including pain medication during postoperative period was performed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
84 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
No Intervention
Arm Description
8 mmHg pressure group
Arm Title
Study group
Arm Type
Experimental
Arm Description
10 mmHg group
Intervention Type
Procedure
Intervention Name(s)
Intraabdominal pressure
Intervention Description
Limited intraabdominal pressure during laparoscopic cholecystectomy between 8 and 10 mmHg.
Primary Outcome Measure Information:
Title
Shoulder tip pain
Description
The shoulder tip pain was assessed by the investigator during postoperative period unfil 48 hours. The measurement of the outcome, the investigator would ask the participant by the clinical record form and questionnair. The answer of the questionnaire is presence or absence of the shoulder pain or pain around the shoulder and scapular region.
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Change of intra-abdominal pressure
Description
The change of intra-abminal pressure was measure by two parameters. Firstly, the adjustment of the pressure during the operation was recorded by the questionnaire. The answer of the questionnaire is the presence or absence of the intra-abdominal pressure change. Secondly, the maximum intra-abdominal pressure which is the highest pressure used during the operation, is measure by the level of the pressure appearing in the laparoscopic station by mmHg unit.
Time Frame
Immediately after surgery
Title
Difficulty of the operation
Description
The difficulty level of the operation which evaluated by the surgeons. The measurement of this outcome by the questionnaire.
Time Frame
Immediately after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > 15 years
Elective procedure of laparoscopic cholecystectomy
Sign to Inform consent
Exclusion Criteria:
Emergency surgery
Concomitant other procedure performed
Deny to participant
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thanida Janbavonkij, M.D.
Phone
(660)909851540
Email
Than_bow@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Narongsak Rungsakulkij, M.D.
Phone
(660)22011527
Email
narongsak.run@mahidol.ac.th
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Narongsak Rungsakulkij, M.D.
Organizational Affiliation
Faculty of Medicine Ramathibodi Hospital, Mahidol University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Medicine, Ramathibodi Hospital, Mahidol University
City
Bangkok
ZIP/Postal Code
10400
Country
Thailand
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Narongsak Rungsakulkij, M.D.
Phone
(660)2011527
Email
narongsak.run@mahidol.ac.th
First Name & Middle Initial & Last Name & Degree
Thanida Janbavonkij, M.D.
Phone
(660)909851540
Email
Than_bow@hotmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
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Optimum-pressure for Reducing Postoperative Shoulder-tip Pain in Laparoscopic Cholecystectomy
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