Clinical Trials Directory

Trials / Completed

CompletedNCT01559285

Effects of Epidurally Administered Ropivacaine Concentration on the Hemodynamic Parameters

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Pusan National University Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

In this trial, the investigators intend to examine whether the concentration of local anesthetics during epidural analgesia could be modulating factor for change of hemodynamics in patients undergoing major upper abdominal surgery.

Detailed description

One hundred and twenty patients scheduled for major abdominal surgery under TEA combined general anesthesia were randomized in a double-blinded method to receive one of three different concentration study solutions in 8 ml of volume after the induction of anesthesia: 0.75% ropivacaine (60 mg), 0.375% ropivacaine (30 mg), or 0.2% ropivacane (16 mg). In each group, the patients were divided into two subgroups at the age of 60 to perform age based analysis. The acquired hemodynamic data after administration of epidural loading dose were compared and analyzed between young and elderly groups in each group.

Conditions

Interventions

TypeNameDescription
DRUG0.75% ropivacaine concentration0.75% ropivacaine 8ml was injected epidurally after induction of general anesthesia
DRUG0.375% ropivacaine concentration0.375% ropivacaine 8ml was injected epidurally after induction of general anesthesia
DRUG0.2% ropivacaine concentration0.2% ropivacaine 8ml was injected epidurally after induction of general anesthesia

Timeline

Start date
2011-11-16
Primary completion
2013-04-19
Completion
2013-04-19
First posted
2012-03-21
Last updated
2017-08-29

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01559285. Inclusion in this directory is not an endorsement.