Continuous Infusions vs Scheduled Bolus Infusions

Recruiting Phase 4 Interventional Study
Surgical Procedure, Unspecified Pain, Postoperative
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
240 (estimated)
Sponsor
Stanford University · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
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.

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Adult patients presenting for nerve block catheters for post-operative analgesia * ASA physical status I, II, or III. Exclusion Criteria: * Pregnancy * Incarceration * Age \<18 * BMI \>35 * Pre-operative opioid use \>30 mg morphine equivalents per day * Inability to communic…
Contacts

Aaron J Deng, BS

408-914-5494

adeng1@stanford.edu

CONTACT