Clinical Trial: Ultrasound-guided Rectus Sheath Block for Post-operative Pain Control Following Umbilical Hernia Repair
Study Status: Completed
Recruit Status: Completed
Study Type: Interventional
Official Title: Ultrasound-guided Rectus Sheath Block for Post-operative Pain Control Following Umbilical Hernia Repair
Brief Summary:
The purpose of this study is to compare the effectiveness of local infiltration to an ultrasound guided nerve block placed by the anesthesiologist for children undergoing umbilical hernia repair.
This is a double-cohort, double blinded, randomized study comparing local infiltration to ultrasound-guided rectus sheath block in children 1 to 17 years of age undergoing epigastric or umbilical hernia repair.
We will first compare pain scores to see if one method is more adequate then the other in providing post-op analgesia. Our second aim is to compare morphine consumption between the two groups.
Our third aim is to measure the levels of local anesthetic in the blood following local anesthetic infiltration or USGRSB.
Detailed Summary:
Healthy children, aged 1 to 17 years of age, undergoing elective umbilical hernia repairs will be considered for this study. After informed consent/assent has been obtained, the subject will be randomized into one of two groups. Group A will receive local infiltration of 0.25% bupivacaine by the surgeon at the end of the subject's surgery. Group B will undergo an ultrasound-guided rectus sheath block using 0.25% bupivacaine prior to incision by an anesthesiologist skilled in the performance of this block.
All subjects will receive a standardized anesthetic for their surgery. Subjects assigned to Group A (local infiltration) will receive 2mcg/kg of fentanyl prior to incision for intra-operative pain management. Subjects assigned to Group B will have their Rectus Sheath Block and no fentanyl will be given at this time.
Fentanyl is a short-acting opioid analgesic. It's duration of action in the dose we will be using is approximately one hour which is close to the expected length of surgery. Therefore, it is not expected to influence the pain management after surgery.
Pain scores will be assessed by a member of the research team. They will be blinded to which technique the subject has been randomized to. This person will not be involved in the direct care of the subject. These observations will be made using an age-appropriate scoring system (FLACC or FACES scale). Scoring will be done every 5 minutes when the subject is in the recovery room and every 30 minutes when they are in Phase II. This will be done until the subject is discharged from the hospital.
Families will be followed by phone for 48 h post discharge, to collect data on medication use.
Sponsor: Seattle Children's Hospital
Current Primary Outcome: pain scores [ Time Frame: 4 hours ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
- morphine consumption [ Time Frame: 4 hours ]
- plasma bupivacaine levels [ Time Frame: 0, 10, 20, 30, 45, 60 minutes after injection ]
Original Secondary Outcome: Same as current
Information By: Seattle Children's Hospital
Dates:
Date Received: February 3, 2009
Date Started: February 2009
Date Completion:
Last Updated: June 10, 2014
Last Verified: June 2014
