25 Participants NeededMy employer runs this trial

Lidocaine + Epinephrine for Postoperative Pain

(REST Trial)

DM
SA
AB
Overseen ByAshley Burke
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Duke University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

Regional anesthesia techniques (or nerve blocks) are used to provide sensory blockade over the abdominal wall. The most established technique is thoracic epidural. This provides bilateral spread but is also associated with neuraxial complications, which has led to a decrease in clinical usage. The rectus sheath block (RSB) is an established regional anesthesia technique used to provide somatic analgesia to the midline anterior abdominal wall by depositing local anesthetic in the posterior rectus sheath, thereby targeting the terminal anterior branches of the lower thoracic intercostal nerves. The conventional approach involves placing the ultrasound (US) probe transversely across the rectus abdominis muscle and advancing the needle in-plane either lateral-to-medial or medial-to-lateral. While this technique achieves spread within the sheath, the cephalocaudal distribution of local anesthetic may be suboptimal, potentially limiting the extent of dermatomal coverage. A longitudinal probe orientation, with needle insertion from cephalad to caudad, may theoretically facilitate a more extensive cranio-caudal spread by aligning the injection axis with the anatomical fascial plane of the posterior rectus sheath. However, the relative efficacy of these two approaches has not been investigated in a controlled, comparative setting. Thus, this randomized, single-blinded trial aims to evaluate the dermatomal sensory distribution and ultrasound-assessed local anesthetic spread achieved by the transverse versus longitudinal in-plane approaches to ultrasound-guided RSB in healthy adult volunteers. To compare the dermatomal sensory block distribution, investigators will use dermatomal mapping with pinprick, and cold.

Are You a Good Fit for This Trial?

This trial is for healthy adults aged 18 or older, weighing over 60 kg, who are in good health (ASA status 1 or 2), can give written consent, and are willing to follow study procedures.

Inclusion Criteria

I am 18 years old or older.
I weigh more than 60kg.
I am willing and able to follow the study's procedures and timeline.
See 2 more

What Are the Treatments Tested in This Trial?

Interventions

  • Lidocaine with Epinephrine

Trial Overview

The study compares two ways of giving a nerve block (rectus sheath block) using lidocaine with epinephrine. It looks at whether placing the ultrasound probe sideways or lengthwise affects how well pain relief spreads across the abdomen.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Longitudinal Approach to the Rectus Sheath BlockExperimental Treatment1 Intervention
Group II: Transverse Approach to the Rectus Sheath BlockActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Duke University

Lead Sponsor

Trials
2,495
Recruited
5,912,000+