CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 68 enrolled
Drug / intervention
Ropivacaine +1 moredrug
Likely dose
0.5% Lidocaine or 0.5% Ropivacaine infused via thoracic paravertebral catheterAI-extracted
Key inclusion· 5
  • Age 18–80 years
  • ASA physical status I–III
  • Weight 60–110 kg
  • Height at least 152 cm (60 inches)
Key exclusion· 12
  • ASA physical status IV or greater
  • Contraindications to bilateral thoracic paravertebral catheter placement
  • Chronic painful conditions
  • Preoperative opioid use

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02849678
NCT02849678N/ACompleted

A Comparison of Lidocaine Versus Ropivacaine for Bilateral Continuous Thoracic Paravertebral Nerve Blocks for Post-bowel Surgery Analgesia

Jacques E. Chelly·interventional·Posted Jul 29, 2016·Updated Mar 20, 2018

In Brief

A clinical study evaluating Ropivacaine and Lidocaine for Postoperative Pain. Completed, enrolled 68 participants across 1 site.

Detailed Summary

This research study is testing whether the local anesthetic lidocaine is as effective as ropivacaine for post-operative pain control in continuous thoracic paravertebral nerve blocks. Ropivacaine and Lidocaine are FDA-approved drugs that has been successfully used in this hospital for post-operative pain control for the past few years, thus has become the standard drugs used for this nerve block. Lidocaine has numerous potential advantages over ropivacaine, such as faster onset of action, better safety profile and greater anti-inflammatory action. Catheters placed near both sides of a patient's spine for postoperative pain control are called thoracic paravertebral nerve blocks and are a part of routine care. Through those catheters, a "numbing" medication, or local anesthetic, to block the transmission of pain from the surgical incision to the spinal cord, thus reducing pain. The research part of the study is whether subjects will receive either the local anesthetic lidocaine or ropivacaine. The goal of this study is to determine whether the lidocaine controls pain better and facilitates a faster recovery after abdominal surgery than ropivacaine. In this research study, the investigators will compare patient-reported pain scores, any additional pain medication requirements for adequate pain control, time it takes for bowel function to return to normal following surgery, as well as the incidence of any side effects, such as numbness and weakness, subjects may experience between those receiving lidocaine versus those receiving ropivacaine. The investigators will screen 100 patients and enroll 60 subjects into this study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 29, 2016
Enrollment StartJan 1, 2008
Primary CompletionNov 1, 2013
Study CompletionMay 1, 2016
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 9.9 years ago

Interventions

Ropivacainedrug

0.5% Ropivacaine will be infused through a catheter placed in the thoracic paravertebral space to block the transmission of pain signals at the level of the spinal nerves from the abdominal incision. It is the local anesthetic used as the standard drug in paravertebral nerve blocks at our institution. It is also used in other nerve block infusions at our hospital and institutions across the country. It will be used as the standard drug to which lidocaine is compared.

Lidocainedrug

Lidocaine will be infused through a catheter placed in the thoracic paravertebral space to block the transmission of pain signals at the level of the spinal nerves from the abdominal incision. At a concentration of 0.5%, Lidocaine has been deemed safe to use for peripheral nerve blocks and analgesia. There are several studies to support this as listed in the references. Compared to ropivacaine, lidocaine is shorter-acting, less cardiotoxic, and safer to use.