Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT03230565

Continuous Infusions vs Scheduled Bolus Infusions

Led by Stanford University · Updated on 2025-12-08

240

Participants Needed

1

Research Sites

443 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Continuous Infusions vs Scheduled Bolus Infusions

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients presenting for nerve block catheters for post-operative analgesia
  • ASA physical status I, II, or III
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Incarceration
  • Age under 18 years
  • Body mass index (BMI) over 35
  • Pre-operative opioid use greater than 30 mg morphine equivalents per day
  • Inability to communicate with investigators by telephone
  • Pre-existing neuropathy of the operative extremity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Stanford University

Stanford, California, United States, 94305

Actively Recruiting

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Research Team

A

Aaron J Deng, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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