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Synera™ for Epidural Needle Insertion

NCT00564785 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 33

Last updated 2007-11-28

No results posted yet for this study

Summary

We hypothesized that the analgesic effect of Synera™ analgesic patch would be superior to traditional infiltration with lidocaine for pain of epidural needle insertion in laboring parturients.

Conditions

  • Pain Associated With Epidural Needle Insertion

Interventions

DRUG

Synera(TM)

Synera(TM) patch applied 20 minutes prior to epidural

OTHER

Placebo patch

placebo patch applied 20 minutes prior to epidural

Sponsors & Collaborators

Principal Investigators

  • Ronald B George, MD FRCPC · IWK Health Centre

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-02-28
Completion
2007-03-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00564785 on ClinicalTrials.gov