Clinical Trials Directory

Trials / Terminated

TerminatedNCT03592056

Hemidiaphragmatic Paralysis With Diluted Continuous Interscalene Plexus Infusions

Incidence of Hemidiaphragmatic Paralysis Using 0.04% Levobupivacaine for Continuous Interscalene Brachial Plexus Blocks in Arthroscopic Shoulder Surgeries

Status
Terminated
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
Clinica las Condes, Chile · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Interscalene brachial plexus block (ISB) constitutes the analgesic criterion standard for shoulder surgery. However, it is associated with a high incidence of hemidiaphragmatic paralysis (HDP) that may not be tolerated by patients with chronic pulmonary disease. Continuous ISBs have not avoided this complication with the reported and regularly used local anesthetic dilutions (i.e. 0.125% bupivacaine, 0.25% ropivacaine, etc). This observational study will register the incidence of HDP in continuous interscalene block (CISB) using a very diluted solution of levobupivacaine (0.04%) in patients undergoing arthroscopic shoulder surgery. The main objective of this study is to determine the frequency of HDP the first postoperative day before patient discharge(POD).

Conditions

Timeline

Start date
2018-08-10
Primary completion
2019-07-23
Completion
2019-07-23
First posted
2018-07-19
Last updated
2020-01-23

Locations

1 site across 1 country: Chile

Source: ClinicalTrials.gov record NCT03592056. Inclusion in this directory is not an endorsement.

Hemidiaphragmatic Paralysis With Diluted Continuous Interscalene Plexus Infusions (NCT03592056) · Clinical Trials Directory