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Trans-incisional vs Laparoscopic Guided Rectus Sheath Block for Pediatric Single Incision Laparoscopic Cholecystectomy

Primary Purpose

Pain, Postoperative

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Trans-incisional rectus sheath block
Laparoscopic guided rectus sheath block
Ropivacaine
Sponsored by
Johns Hopkins All Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Pain, Postoperative

Eligibility Criteria

10 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged 10-21 years old undergoing single-incision laparoscopic cholecystectomy

Exclusion Criteria:

  • Patients with choledocolithiasis, gallstone pancreatitis, or sickle cell disease
  • Allergy to bupivacaine
  • Concurrent surgical procedure
  • Developmental delay or neurologic diagnosis that would interfere with post- operative pain score assessment
  • Chronic pain medication use, chronic pain disorder or complex regional pain syndrome
  • Anesthesiologist classification of III or greater

Sites / Locations

  • Johns Hopkins All Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Trans-incisional rectus sheath block

Laparoscopic guided rectus sheath block

Arm Description

rectus sheath block under direct visualization through the umbilical incision by the attending surgeon

rectus sheath block under direct laparoscopic visualization by the attending surgeon

Outcomes

Primary Outcome Measures

Post Operative Pain Rating
Using the Wong-Baker FACES Pain Rating Scale (WBFPRS). The WBFPRS is a visual pain rating scale in which the participant looks at pictures of faces depicting levels of pain and chooses the one that most closely resembles their own pain. The scale ranges from 0 "no hurt" to 10 "Hurts Worst."

Secondary Outcome Measures

Operative Time
Operative time is measured as the time between X and Y. Reported in minutes.
Use of Post-operative Intravenous/Oral Opioid and Non-opioid
Amount of postoperative intravenous/oral opioid and non-opioid medications received by patient. This is being recorded as Morphine milligram equivalents (MME)/kilogram(kg) for days 1-5.
Time to First Rescue Analgesic
Amount of time in minutes until the first analgesic is given postoperatively.
Number of Participants With Side Effects
Number of participants with side effects such as nausea, vomiting, allergic reactions.
Number of Participants With Complications
Number of participants with complications such as infection, bleeding, intravascular injection, bowel puncture.
Total Number of Complications
Total number of complications such as infection, bleeding, intravascular injection, bowel puncture.

Full Information

First Posted
July 8, 2015
Last Updated
January 4, 2021
Sponsor
Johns Hopkins All Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02494336
Brief Title
Trans-incisional vs Laparoscopic Guided Rectus Sheath Block for Pediatric Single Incision Laparoscopic Cholecystectomy
Official Title
Trans-incisional Rectus Sheath Block Versus Laparoscopic Guided Rectus Sheath Block for Pediatric Single Incision Laparoscopic Cholecystectomy: A Prospective, Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
June 2015 (undefined)
Primary Completion Date
October 1, 2018 (Actual)
Study Completion Date
October 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins All Children's Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a prospective, double-blinded, randomized controlled study comparing the efficacy of trans-incisional rectus sheath block to laparoscopic guided rectus sheath block for pediatric single-incision laparoscopic cholecystectomy (SILC). umbilical hernia repair in children. Patients aged 10-21 years old undergoing SILC for cholelithiasis, cholecystitis, or biliary dyskinesia will be screened for study inclusion. Eligible patients and their parents/guardians will be approached and, if agreeable, consented for the study pre-operatively. Patients will be randomized to receive either trans-incisional rectus sheath block or intra-operative rectus sheath block under direct laparoscopic visualization. Both will be done by the attending pediatric surgeon. The patient, patient guardians, select research team members, and Post anesthesia care unit (PACU) staff will be blinded to the method of analgesic administration.
Detailed Description
Regional anesthesia has been increasingly utilized for providing post-operative analgesia for a number of surgical procedures in children. Rectus sheath block and local anesthetic infiltration of the surgical site are two common modes for providing post-operative analgesia. Studies comparing the two modes have shown ultrasound-guided rectus sheath block to improve immediate pain scores and reduce use of post-operative analgesia in pediatric patients undergoing umbilical hernia repair. However, these studies have compared pre-incisional ultrasound-guided rectus sheath block to post-operative local anesthetic infiltration as a subcutaneous and/or intradermal injection. Also, to our knowledge, there are no studies evaluating the use or efficacy of laparoscopic guided rectus sheath block for pediatric single-incision laparoscopic surgery. Single-incision surgery involves performing abdominal operations though a single, small incision, usually located at the umbilicus. The purpose of this study is to compare the efficacy of trans-incisional rectus sheath block to intra-operative infiltration of the rectus sheath under direct laparoscopic visualization via an intra-abdominal approach for providing post-operative analgesia following single-incision laparoscopic cholecystectomy (SILC) in children. The investigators propose a prospective study where pediatric patients who are undergoing single-incision laparoscopic cholecystectomy will be randomized pre-operatively to receive either a trans-incisional rectus sheath block after facial closure but prior to skin closure or intra-operative infiltration of the rectus sheath under direct laparoscopic visualization after cholecystectomy. The primary outcome is the post-operative pain rating based on the Wong-Baker Faces Pain Rating Scale (WBFPRS) following SILC. Additional outcomes measured will include: operative times, the use of intravenous/oral opioid and/or non-opioid medication in the post-operative period, duration of analgesia following surgery based on time to first rescue analgesic, intra-operative hemodynamic changes, post-operative hemodynamic changes, incidence of side-effects, and complications. Patients/patient guardians will receive a sheet to document post-operative WBFPRS scores, oral opioid and non-opioid medication administration once discharged to home for a total of 5 days.

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
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Trans-incisional rectus sheath block
Arm Type
Active Comparator
Arm Description
rectus sheath block under direct visualization through the umbilical incision by the attending surgeon
Arm Title
Laparoscopic guided rectus sheath block
Arm Type
Active Comparator
Arm Description
rectus sheath block under direct laparoscopic visualization by the attending surgeon
Intervention Type
Procedure
Intervention Name(s)
Trans-incisional rectus sheath block
Intervention Description
After removal of the gallbladder, a predetermined volume of 0.2% ropivacaine (1cc/kg, max dose 10cc, divided into equal doses bilaterally) will be administered under direct visualization into the rectus sheath bilaterally by the attending surgeon. This will be done after closure of the fascial incision but prior to closure of the skin incision.
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic guided rectus sheath block
Intervention Description
After removal of the gallbladder, a predetermined volume of 0.2% ropivacaine (1cc/kg, max dose 10cc, divided into equal doses bilaterally) will be administered intra-abdominally under direct laparoscopic visualization into the rectus sheath bilaterally by the attending surgeon.
Intervention Type
Drug
Intervention Name(s)
Ropivacaine
Other Intervention Name(s)
Naropin
Intervention Description
Ropivacaine is a long-acting local anesthetic. It has been shown to be effective for peripheral nerve, caudal, and lumbar/thoracic epidural blocks and produce less motor blockade than bupivacaine after caudal administration. It will be the local anesthetic used to perform the rectus sheath block for both arms.
Primary Outcome Measure Information:
Title
Post Operative Pain Rating
Description
Using the Wong-Baker FACES Pain Rating Scale (WBFPRS). The WBFPRS is a visual pain rating scale in which the participant looks at pictures of faces depicting levels of pain and chooses the one that most closely resembles their own pain. The scale ranges from 0 "no hurt" to 10 "Hurts Worst."
Time Frame
5 days
Secondary Outcome Measure Information:
Title
Operative Time
Description
Operative time is measured as the time between X and Y. Reported in minutes.
Time Frame
1 day
Title
Use of Post-operative Intravenous/Oral Opioid and Non-opioid
Description
Amount of postoperative intravenous/oral opioid and non-opioid medications received by patient. This is being recorded as Morphine milligram equivalents (MME)/kilogram(kg) for days 1-5.
Time Frame
5 days
Title
Time to First Rescue Analgesic
Description
Amount of time in minutes until the first analgesic is given postoperatively.
Time Frame
1 day
Title
Number of Participants With Side Effects
Description
Number of participants with side effects such as nausea, vomiting, allergic reactions.
Time Frame
5 days
Title
Number of Participants With Complications
Description
Number of participants with complications such as infection, bleeding, intravascular injection, bowel puncture.
Time Frame
30 days
Title
Total Number of Complications
Description
Total number of complications such as infection, bleeding, intravascular injection, bowel puncture.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 10-21 years old undergoing single-incision laparoscopic cholecystectomy Exclusion Criteria: Patients with choledocolithiasis, gallstone pancreatitis, or sickle cell disease Allergy to bupivacaine Concurrent surgical procedure Developmental delay or neurologic diagnosis that would interfere with post- operative pain score assessment Chronic pain medication use, chronic pain disorder or complex regional pain syndrome Anesthesiologist classification of III or greater
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicole M Chandler, MD
Organizational Affiliation
Johns Hopkins All Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins All Children's Hospital
City
Saint Petersburg
State/Province
Florida
ZIP/Postal Code
33701
Country
United States

12. IPD Sharing Statement

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Trans-incisional vs Laparoscopic Guided Rectus Sheath Block for Pediatric Single Incision Laparoscopic Cholecystectomy

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