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Sponsors and Collaborators: |
IWK Health Centre Duke University |
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Information provided by: | IWK Health Centre |
ClinicalTrials.gov Identifier: | NCT00564785 |
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.
Condition | Intervention | Phase |
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Pain Associated With Epidural Needle Insertion |
Drug: Synera(TM) Other: Placebo patch |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver), Placebo Control, Parallel Assignment, Efficacy Study |
Official Title: | A Randomized, Double-Blind, Controlled Trial of the Synera™ vs. Lidocaine for Epidural Needle Insertion in Laboring Women |
Enrollment: | 33 |
Study Start Date: | February 2007 |
Study Completion Date: | March 2007 |
Arms | Assigned Interventions |
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Placebo: Placebo Comparator |
Other: Placebo patch
placebo patch applied 20 minutes prior to epidural
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Synera(TM): Experimental |
Drug: Synera(TM)
Synera(TM) patch applied 20 minutes prior to epidural
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Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, North Carolina | |
Duke University Medical Center | |
Durham, North Carolina, United States, 27710 |
Principal Investigator: | Ronald B George, MD FRCPC | IWK Health Centre |
Study ID Numbers: | DWA-2007-001 |
Study First Received: | November 27, 2007 |
Last Updated: | November 27, 2007 |
ClinicalTrials.gov Identifier: | NCT00564785 |
Health Authority: | United States: Institutional Review Board |
Lidocaine Pain |