Post-operative Pain Control-TAP Block Using Exparel vs. Marcaine for Hernia Repairs

Inguinal Hernia Clinical Trial

Official title:

The Evaluation of Post-operative Pain Control With a TAP Block Using Exparel vs. Marcaine for Hernia Repairs

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05177991
• Other study ID #: Anesthesia_Hernia_Pain
• Status: Recruiting
• Phase: Early Phase 1
• Start date: March 1, 2022
• Est. completion date: December 31, 2024

Study information

• Verified date: October 2023
• Source: Our Lady of the Lake Hospital
• Contact: Christine LeBoeuf, DNP
• Phone: 225-765-5956
• Email: Christine.LeBoeuf[@]fmolhs.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

While studies have shown improved postoperative pain control with TAP blocks after inguinal and ventral hernia repair, data comparing Liposomal bupivacaine (Exparel) to bupivacaine alone in formulation of the TAP block is particularly scarce. Therefore, we designed a prospective, randomized trial comparing the postoperative pain control in minimally invasive ventral and inguinal hernia repair patients who receive an Exaparel-based TAP block compared to the traditional bupivacaine (Marcaine) TAP block.

Description:

Approximately 200 patients in the study will be randomized to one of two arms: TAP block with Exparel or TAP block with bupivacaine. Randomization will be performed using a permuted block randomization algorithm (Ex. AABBABABABBABBAA, where A=Exparel group and B=Bupivacaine group). Only the participant will be blinded to the arm assignment as the knowledge of the assignment for the surgeon and anesthesiologist is needed. The bilateral TAP block will be performed by the department of anesthesia under ultrasound guidance using 20cc of local anesthetic per side. Additional local anesthetic will be supplied by the surgeon at the incision sites. Both of these anesthetics being evaluated and the dosage are commonly administered as standard of care (SOC). The choice of anesthetic used is up to the discretion of the surgeon in most instances. The patients will be blinded to which local anesthetic they receive. Operative technique will be standardized amongst all participating surgeons. All patients with ventral hernias will undergo an IPOM+ technique detailed by primary closure of the defect in addition to circumferential mesh fixation with a running suture. Three or four trochars will be used ranging from 5-12mm in size. Mesh selection will be at the discretion of the surgeon with a minimum of 5cm overlap of the original defect in all directions. Defect size will be measured intraoperatively with a ruler intra-abdominally. All patients with an inguinal hernia will undergo a transabdominal preperitoneal hernia repair with mesh placement. Three or four trochars ranging from 5-12mm will be used. Size of mesh and fixation of mesh at one or two points will be at the surgeon's discretion. The length of surgery will be recorded. The patients will be given a packet of VAS pain assessments to take home with pre-marked time intervals to fill out at 2h, 6h, and 12h post operatively as well as every 12 hours thereafter. The patients will also be asked to record how many narcotic medications they will be consuming on a daily basis. Our team will contact patients daily to collect the data verbally which will also serve as a reminder to patients to complete this task faithfully. Each patient will follow up at one week and provide the surgeons with the packet of VAS assessments as well as bring in any excess narcotics that they did not consume. Each patient will also be told to take tylenol 500mg every 6 hours for the first 96 hours and to record whether they take any additional alternative pain medications (NSAIDs, muscle relaxants, gabapentinoids). Upon discharge, patients will be prescribed 15 pills of 5mg hydrocodone-325mg acetaminophen to be taken every 6 hours as needed for severe pain. Data collection will include demographics of the patients including age, sex, ASA status, height/weight, BMI, preoperative pain level and previous abdominal surgeries. Intraoperative variables will include defect size, ventral vs. inguinal, number of trochar, mesh size and type, operative time. Postoperative collection will include pain scores as outlined above and narcotic use. Data analysis will include differences, if any, in post operative pain scores as well as narcotic use. This will be stratified to the inguinal hernia group vs. ventral hernias and the ventral hernia group will be stratified to size of defect and length of surgery.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years of age or older
• Have a ventral or inguinal hernia requiring surgical repair

Exclusion Criteria:

• Less than 18 years of age
• Chronic pain patients
• Having a defect >10 cm in transverse dimension
• Having a defect <4 cm
• Has an allergy to bupivacaine
• Has recurrent hernias as per medical history
• A TAP block performed at any time aside from just prior to the start of the procedure
• If bupivacaine is mixed with other anesthetics
• Under the instance of an emergency surgery (trauma)
• Concomitant surgery
• History of EtOH abuse
• History of liver/kidney dysfunction
• If the procedure must be converted to open
• Inidividual's weight < 50kg
• Individual's BMI > 45

Related Conditions & MeSH terms

• Hernia
• Hernia, Inguinal
• Hernia, Ventral
• Inguinal Hernia
• Pain, Postoperative
• Ventral Hernia

Intervention

Drug:
• Liposomal Bupivacaine
20cc of Liposomal Bupivacaine for TAP block
• Bupivacaine
20cc of Bupivacaine for TAP block

Locations

Country	Name	City	State
United States	Karl LeBlanc	Baton Rouge	Louisiana

Sponsors (2)

Lead Sponsor	Collaborator
Leslie Son	Our Lady of the Lake Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Subjective Pain Scores using Visual Analog Scale (VAS)	Lower mean daily post-operative pain scores between participants in the Exparel vs. Bupivacaine arms recorded multiple times over the observation period. The pain scale is 0-10 with 0 being no pain to 10 being the worst pain possible.	For 1 week post-operation
Secondary	Opioids Used Post-Operatively compared in anesthesia arms	The amount of opioid pills taken, as measured by morphine equivalents, is reduced depending on the type of anesthetic used during the TAP block. We will be measuring the post operative opioid usage by asking the patients how many narcotic pills they take daily after surgery for one week. Variability comes into play if we prescribe different doses of Norco or if we use Percocet, therefore we will standardize this by converting these differing dosages in to morphine equivalents for both groups.	For 1 Week post-operation
Secondary	Opioids Used Post-Operatively related to Hernia Size and Surgical Time	A decrease in the total number of opioid pills taken post-operatively compared to the total surgical time and how large the hernia defect is. Increased surgical times and larger hernias may play a role in the amount of pain medication an individual may need post-operatively.	After 1 week post-operation