Clinical Trials Directory

Trials / Completed

CompletedNCT00197327

Dilute Versus Concentrated Epidural Bupivacaine in Labor

Analgesia Requirement and Maternal Satisfaction Following Epidural PCA in Nulliparous Labor: the Effect of a Four-Fold Change in Local Anesthetic Concentration.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
60 (planned)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

This study studies labor epidural analgesia and compares dilute (0.0625%) with concentrated (0.25%) bupivacaine. We hypothesize that patients randomize to receive the concentrated drug will require more drug, will have a more profound motor block, will be more likely to require instrumental delivery and will be less satisfied than those receiving dilute epidural drugs.

Detailed description

This study examines the effect of two different local anesthetic concentrations used for epidural analgesia in labor. Patients are randomized to receive epidural bupivacaine, either as a concentrated (0.25%), or a dilute (0.0625%) solution, both administered by patient-controlled epidural analgesia (PCEA).

Conditions

Interventions

TypeNameDescription
DRUGEpidural bupivacaine (0.25% versus 0.0625%)

Timeline

Start date
1998-02-01
Completion
2000-03-01
First posted
2005-09-20
Last updated
2006-03-03

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00197327. Inclusion in this directory is not an endorsement.