Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01775605

Study of Use of Synera for Pain During Local Skin Infiltration With Lidocaine Before Epidural Placement

Randomized Study of the Use of Synera for Pain Relief During Local Lidocaine Needle Skin Infiltration for Epidural Placement in Subjects Undergoing Elective Cesarean Section.

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Northwell Health · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

Local infiltration with lidocaine prior to epidural placement for cesarean section, although brief, can be painful. This pain can lead to increased anxiety and distress, adversely affecting patient's overall experience. This study proposes to examine the application of Synera pain patch prior to lidocaine infiltration to reduce this pain and anxiety. The primary objective of this study is to determine the effect of the Synera on maternal experience during epidural placement. The efficacy of Synera pain patch in reducing subject pain during skin infiltration with lidocaine prior to epidural placement in subjects presenting for scheduled cesarean section will be assessed.

Conditions

Interventions

TypeNameDescription
DRUGSyneraSynera Pain Patch

Timeline

Start date
2013-11-01
Primary completion
2014-11-01
Completion
2014-11-01
First posted
2013-01-25
Last updated
2015-05-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01775605. Inclusion in this directory is not an endorsement.