Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00848679

Investigating the Novel Observation of Right-left Difference in Uterine Artery Vascular Resistance in Pre-eclampsia

Investigating the Novel Observation of Right-left Difference in Uterine Artery Vascular Resistance in Pre-eclampsia: A Double-blinded, Randomized, Placebo-controlled Study to Assess the Dose-dependent Effect of Epidural Lidocaine on Right-left Uterine Artery Blood Flow Differences in Pre-eclampsia, With Healthy Term Pregnant and Non-pregnant Controls

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Withdrawn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

Summary

The investigators previously demonstrated that epidural ropivacaine reduces uterine artery vascular resistance in a dose dependent manner in pre-eclampsia. The investigators also noted a marked right-left difference in vascular resistance between paired uterine arteries, which was almost completely abolished following epidural ropivacaine. However, this novel observation was not a stated outcome variable before the study began. This study assesses right-left difference in vascular resistance between paired uterine arteries as a primary end-point, assesses the dose-response effect of epidural lidocaine and compares the effect observed in pre-eclampsia with that in two control populations (term normal pregnancy and non-pregnant controls).

Conditions

Interventions

TypeNameDescription
DRUGEpidural lidocaineEpidural 2% lidocaine, administered in 5mL incremental boluses. Looking at dose-response effect.
DRUGEpidural lidocaine 2%5 x 5ml boluses of either epidural lidocaine 2% or epidural saline

Timeline

Start date
2009-03-01
Primary completion
2009-10-01
Completion
2009-10-01
First posted
2009-02-20
Last updated
2019-09-12

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00848679. Inclusion in this directory is not an endorsement.