About this trial

The goal of the study is to compare continuous infusions and scheduled bolus infusions for peripheral nerve blocks and their effect on post-surgical pain.

Eligibility criteria

Qualifiers

Adult patients presenting for nerve block catheters for post-operative analgesia

ASA physical status I, II, or III.

Disqualifiers

Pregnancy

Incarceration

Age <18

BMI >35

Trial design

Treatments tested in this trial

  • Ropivacaine
  • Ropivacaine

Treatment groups

240 Participants
are divided into 2 treatment groups

Locations

1
Stanford University94305, StanfordCalifornia, United States

Sponsors and collaborators

Stanford University

Lead sponsor