Clinical Trials Directory

Trials / Completed

CompletedNCT03480984

Continuous Versus Intermittent Bolus Infusion of Paravertebral Blocks for Thoracic Surgery

A Comparison Between Continuous Versus Intermittent Bolus Infusion of Paravertebral Blocks for Thoracic Surgery: A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The researchers are trying to determine pain medication consumption in the first 24 hours after surgery in patients given the standard continuous infusion of local anesthetic versus patients given the same total dose via programmed intermittent dosing. Both groups will receive the option of patient controlled pain medication as well as the same dose of pre-programmed pain medication. The only difference is the rate of administration: continuous vs. hourly intervals.

Conditions

Interventions

TypeNameDescription
OTHERProgrammed Intermittent Bolus6 mL 0.2% ropivacaine hourly, starting on arrival to PACU, given via an hourly programmed bolus
OTHERContinuous Infusion6 mL 0.2% ropivacaine hourly, starting on arrival to PACU, given via continuous infusion

Timeline

Start date
2018-02-05
Primary completion
2020-01-05
Completion
2020-01-31
First posted
2018-03-29
Last updated
2020-04-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03480984. Inclusion in this directory is not an endorsement.