Optimum-pressure for Reducing Postoperative Shoulder-tip Pain in Laparoscopic Cholecystectomy

Sponsor
Mahidol University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04212936
Collaborator
(none)
84
1
2
30.2
2.8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Intraabdominal pressure
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
84 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Treatment
Official Title:
Optimum-pressure for Reducing Postoperative Shoulder-tip Pain in Laparoscopic Cholecystectomy, a Prospective Randomized Controlled Trial
Actual Study Start Date :
Dec 25, 2019
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Jun 30, 2022

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group

8 mmHg pressure group

Experimental: Study group

10 mmHg group

Procedure: Intraabdominal pressure
Limited intraabdominal pressure during laparoscopic cholecystectomy between 8 and 10 mmHg.

Outcome Measures

Primary Outcome Measures

  1. Shoulder tip pain [48 hours]

    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

  1. Change of intra-abdominal pressure [Immediately after surgery]

    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.

  2. Difficulty of the operation [Immediately after surgery]

    The difficulty level of the operation which evaluated by the surgeons. The measurement of this outcome by the questionnaire.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age > 15 years

  2. Elective procedure of laparoscopic cholecystectomy

  3. Sign to Inform consent

Exclusion Criteria:
  1. Emergency surgery

  2. Concomitant other procedure performed

  3. Deny to participant

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Medicine, Ramathibodi Hospital, Mahidol University Bangkok Thailand 10400

Sponsors and Collaborators

  • Mahidol University

Investigators

  • Principal Investigator: Narongsak Rungsakulkij, M.D., Faculty of Medicine Ramathibodi Hospital, Mahidol University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Narongsak Rungsakulkij, Assistant Professor, Mahidol University
ClinicalTrials.gov Identifier:
NCT04212936
Other Study ID Numbers:
  • MURA2019/1005
First Posted:
Dec 30, 2019
Last Update Posted:
Feb 25, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 25, 2021